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Pharma Field Sales - District Business Manager (DBM)-Hershey, PA Job (Hershey, PA, US)

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Requisition ID 17481BR
Title Pharma Field Sales - District Business Manager (DBM)-Hershey, PA
Job Category Field Sales
Job Description Pharma Field Sales - District Business Manager (DBM)-Hershey, PA

PURPOSE:
To develop and lead sales teams in the execution of sales strategies that increase profitability to maximize sales objectives. Works with RBD to manage, train, develop staff, and prepare regional budget and business plans. This is an entry level district business manager position.

RELATIONSHIPS:
Reports to the Regional Business Director. Manages a region’s sales force, and has direct supervisory responsibility for Pharmaceutical Sales Representatives. Works closely with RBD, peers and the home office to achieve sales objectives and to ensure the development of people. Other relationships include physicians, key accounts, co-promotion partners, associations, field and home office personnel.

PRINCIPAL ACCOUNTABILITIES:

BUSINESS PLANNING
•Work to develop a full understanding of the content and then execute the regional business plan to achieve the fulfillment of Plan objectives/requirements. This includes delivery-of-care system delineation, account targeting, needs assessment, and program implementation.
•Execute regional level account targeting strategy in business unit to fulfill regional account targeting strategy requirements.
•Manage business unit customer needs assessment. Apply assessment frameworks against accounts in region by overseeing DCS account assessment activities. Identify program/service requirements for addressing needs. Work with the VP Diabetes Sales, Field Sales, Regional Directors and appropriate home office management to feed requirements into program development (contracting, marketing programs).
•Oversee regional account relationship development/management. Manage critical regional account relationships and set account relationship development objectives for regional staff.
•Manage regional resource allocation.
•Monitor regional program/initiative effectiveness.
•Monitor performance against strategic account management objectives/directives.

COORDINATION/PARTNERSHIP
•Ensure contractual requirements are met for the region (# of physician calls per day).
•Work with RBD, DBMs, home office and CSO counterparts to gain insight into programs and initiatives.
•Gain an understanding of regional level coordination between field resources, intra-organization resources and inter-organizational resources. Work with RBD to incorporate district.
•Ensure appropriate level of coordination to attain regional business plan objectives.

ADMINISTRATION
•Communicate Regional activity of competitive products through timely submission of monthly highlight reports as directed.
•Review and audit expense reports.
•Evaluate appropriate use of regional resources to ensure attainment of profitability goals.
•Develop and monitor performance against regional budgets.
•Establish and oversee regional implementation, and monitor adherence to administrative policies and procedures.
•Ensure timely and accurate submission of administrative requirements.

ADHERE TO AND SUPPORT COMPANY POLICIES, PROCEDURES AND SALES/MARKETING DIRECTION. IMPLEMENT COMPANY POLICIES, PROCEDURES AND SALES/MARKETING DIRECTION THROUGHOUT THE RBU
•Monitor and reinforce the use of the Sales Force Automation System.
•Ensure timely and accurate transmission of DCS call data.
•Adhere to the Prescription Drug Marketing Act of 1987 and all related Novo Nordisk policies regarding the judicious use of physician samples and stock items.

DEVELOPMENT OF PEOPLE/MANAGEMENT
•Fill open territories with high quality talent within 6 weeks.
•Ensure that reporting personnel have Performance Achievement Plans with annual goals and measurements that are consistent with the priorities of the business, and that interim reviews are held so that their work is focused on those priorities, and they understand their level of accountability for results and the measurement process.
•Manage the application and communication of all Novo Nordisk policies, procedures, and Novo Nordisk Way of Management.
•Ensure that development and training plans are in place for all reporting personnel to enable the achievement of goals and capability to assume increased levels of responsibility.
ATTAIN AND MAINTAIN PROFICIENT LEVELS OF NNPI AND COMPETITIVE PRODUCT KNOWLEDGE
•Continuously improve the knowledge of Novo Nordisk products, competitive products, and management skills through ongoing home study and participation in company sponsored/approved training programs.

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS:

• At least 5 Years Progressive Pharmaceutical/Healthcare Sales experience required
• 2 Years Previous Supervisory experience preferred
• Bachelor Degree required from College or University accredited by an organization recognized by the US Department of Education; major in Business or Marketing preferred.
• Top 20% sales ranking for 1 out of last 2 years, documented (Regionally)

OTHER:
•Works within NNPI’s established policies and procedures and ensures alignment of their work to Novo Nordisk Fundamentals.
•Minimum of 5 years of progressive pharmaceutical/healthcare sales experience required.
•Significant record of sales accomplishments.
•Two years previous supervisory experience preferred.
Department SALES - HERSHEY PA
Position Location US - Field Based - Across US
City Hershey
State/Provinces US - PA
Degree Required Bachelor's Degree Required
Percent Travel 20 - 30%

Process Engineer I - Line Filler 36 Proj Job (clayton, NC, US)

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Requisition ID 17497BR
Title Process Engineer I - Line Filler 36 Proj
Job Category Engineering
Job Description Position Purpose:
Serve as the work package owner for procurement, installation and start-up of a new Cartridge Line Filler within the aseptic production area.
Improve system and equipment reliability for the core processes to meet all customer, business and regulatory requirements through the following activities:
•People Focus
•Equipment Focus
•Standards “Gatekeeper”

Education: BS in Engineering/related field or Equivalent (experience + education)

Experience: 2-5+ years engineering experience in Maintenance, Design, Process Improvement; cLean 1-Star

Technical/Process/Functional Knowledge: Knowledgeable in the following systems: Instrument and Electrical, Mechanical, Control/SCADA/PLCs, Process Improvement Methodologies, Root Cause Analysis (RCA)

Physical Requirements:
Ability to work in confined spaces and near operating equipment.
Ability to work in loud noise environments
Ability to travel internationally.Ability to work hours necessary to support production and maintenance activities.
Department Line Filler 36 Project
Position Location US - Clayton, NC
City clayton
State/Provinces US - NC
Degree Required Bachelor's Degree Required
Percent Travel 0 - 10%

Manager-Sr. Manager, Regulatory Affairs - Regulatory Intelligence Job (Princeton, NJ, US)

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Requisition ID 17435BR
Title Manager/Sr. Manager, Regulatory Affairs - Regulatory Intelligence
Job Category Regulatory Affairs
Job Description PURPOSE:

Manage Regulatory Intelligence and Registration Information Management System (RIMS) support for the Regulatory Affairs department. Proactively monitor the US regulatory environment, identify and analyze information pertinent to Novo Nordisk, and communicate such information to stakeholders. Ensure that RIMS activities for Regulatory Affairs are carried out according to established procedures. Contribute to additional Regulatory Intelligence and RIMS projects as needed. Assist Regulatory Affairs Management in assuring Novo Nordisk compliance with internal SOPs and Federal and State regulations.

RELATIONSHIPS:

Reports to Regulatory Operations and Innovation management. Works with personnel in other departments including Marketing, CMR, Legal, as well as counterparts in NN/AS Regulatory Affairs and the RA Global Services Center (GSC) in Bangalore. Works closely with RA Therapeutic Area (TA) team members on Regulatory Intelligence and RIMS activities. A positive approach to projects and willingness to maintain constructive and positive interactions with coworkers is necessary.

ESSENTIAL FUNCTIONS:

• Assist supervisor in the coordination of information flow from and to pharmaceutical organizations such as PhRMA, BIO and AdvaMed to promote Novo Nordisk positions in relation to regulatory environment.
• Explore internal and external regulatory intelligence for the preparation and submission of regulatory documents, assuring NNI compliance with Federal and State Regulations and tracking submission status for corporate database.
• Identify and analyze relevant external intelligence sources e.g. FDA, HHS, PHRMA, US Government, NN Project intraweb, competitor website, and industry publications. Provide summaries of information to product/project teams.
• Maintain surveillance of regulatory environment and competitor development and provide evaluation to product/project teams.
• Maintain up-to-date general knowledge of FDA guidances and regulations to facilitate collection and evaluation of ongoing regulatory climate.
• Monitor and evaluate regulatory landscape e.g. Federal, State, HHS, FDA communications/rules/guidelines for information pertinent to Novo Nordisk business.
• Publish and disseminate intelligence (weekly Highlights or summary of pertinent articles) in a timely manner, to relevant groups within RA/CMR, NN-US (e.g. Legal, Marketing, Sales) or Headquarters.
• Manage collection of research, analyze information, and compose letters on Novo Nordisk opinions/position on FDA draft guidances, proposed rules etc. to provide comments on regulatory initiatives.
• Manage input of submission information into Regulatory Information Management System (RIMS) through RA Global Services Center (GSC), provide required data to Headquarters and GSC, and ensure that all US data in RIMS is complete, correct and handled within required timelines.
• Collaborate with Regulatory Affairs TA to ensure that RIMS data are specifically aligned with FDA submissions.
• Work with colleagues in HQ and GSC on projects and initiatives supporting RIMS activities.
• Provide RIMS training to Regulatory Affairs department.
• Assist with overflow in other areas as needed and handle other duties and/or special projects as assigned by Regulatory Affairs management.

PHYSICAL REQUIREMENTS:

• Approximately 10% overnight travel

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS
• A BA/BS required (life science or related area); advanced degree preferred
• A minimum of 6 years related regulatory affairs experience required
• Advanced knowledge of pertinent FDA regulations
• Experience with regulatory intelligence activities and pharmaceutical registration databases is preferred
• Detail & deadline oriented; well organized
• Excellent verbal & written communication skills
• Good interpersonal skills; ability to interact with staff on all levels
• Knowledge of diabetes and diabetes management beneficial
• Previous supervisory/management experience advantageous
• Works independently with minimal supervision
• An advanced proficiency in Microsoft Office Suite required
• Effective personal time management and project management skills
Department CMR - REG AFFAIRS (5a)
Position Location US - Princeton, NJ
City Princeton
State/Provinces US - NJ
Degree Required Bachelor's Degree Required
Percent Travel 0 - 10%

ASSOCIATE MANAGER - PRODUCT COMMUNICATIONS Job (Princeton, NJ, US)

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Requisition ID 16903BR
Title ASSOCIATE MANAGER - PRODUCT COMMUNICATIONS
Job Category Marketing
Job Description PURPOSE:
This position is accountable for helping manage diabetes product communications at Novo Nordisk Inc. targeting key external and internal stakeholders. This position is a partner to diabetes brand teams, participating in extended brand team meetings, and providing communications counsel and direction, and program specific recommendations (specifically as it relates to tactical planning). This position also collaborates with various teams to ensure close alignment, integration and coordination of related strategies. This position will help with the execution of strategic branded public relations campaigns and tactics to ensure successful program execution and measurement.

RELATIONSHIPS:
• Key external relationships include media, diabetes patient and professional opinion leaders; professional and patient/consumer third party groups; and public relations agencies.
• This position reports to the Senior Manager, Product Communications, Diabetes Marketing, and interacts with all areas within Novo Nordisk Inc. and Novo Nordisk A/S regarding product communications programs, goals and needs. In addition to Diabetes Marketing, this position partners with Public Affairs, Legal, Regulatory, Medical, Compliance, BioPharm and other business functions. Key relationships in Novo Nordisk A/S include global marketing, corporate communications, and corporate branding.

ESSENTIAL FUNCTIONS:

Issues Management:
• Develops communications plan around issues, collaborating across work groups to ensure accurate information to the media and consumers.
• Prepares for and manages issues.
• Strategizes and collaborates with Public Affairs to ensure effective integration, alignment, and collaboration on execution to minimize impact on overall Company reputation.

Measurement:
• Charts and reports progress and adjusts plans/tactics accordingly.
• Collaborates with brands to establish meaningful and brand-aligned objectives and measurements for product communications programs that are aligned with business goals.
• Ensure integration of branded programs and messaging into media efforts, alignment on measurement tools.
• Holds agencies accountable for delivering on measurement targets.

Product Communications:
• Accountable for executing programs within budget parameters. Accountable to manage the budget process for designated scope. Monitor agency expenses by looking for opportunities to maximize value while minimizing agency costs.
• Assists in the development and implementation of proactive product communications and media relations strategies to support the brand/portfolio business goals and strategies of Novo Nordisk. Programs are closely aligned to specific business objectives. Other projects and responsibilities, as assigned.
• Cultivates relationships with patients and celebrity ambassadors using NNI brands, contract negotiation, and program management as assigned.
• Follows internal and external procedures in managing contracts. Regularly tracks and reconciles expenses to ensure budget is on track.
• Helps drive positive media coverage for assigned Novo Nordisk products in various media venues to enhance visibility of company and its brands.
• Identifies external resources needed to implement public relations programs; directs agency or consultants in tactical execution of various programs; and conducts reviews/assessments of agency performance twice per year.
• Prepares/coaches internal spokespeople for media interviews and external speaking opportunities.

PHYSICAL REQUIREMENTS:
Approximately 20% overnight travel.

DEVELOPMENT OF PEOPLE:
Not applicable.

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS
• A Bachelors or higher degree in journalism, public relations, English or a related communications discipline required.
• Ability to handle multiple priorities and coordinate contacts with various vendors and internal customers.
• At least 4 years of product communications, media or public relations experience required, preferably in the pharmaceutical industry.
• Demonstrated ability to treat confidential matters with appropriate discretion.
• Media relations skills, pre-existing relationships with reporters, patient opinion leaders, etc. is desired.
• Proven ability to effectively manage projects.
• Proven ability to solve difficult problems and overcome conflict situations with effective solutions.
• Proven strategic planning, issues/crisis management skills are essential for this position.
• Strong interpersonal, communication, and customer service skills.
• The ability to function effectively as part of a multidisciplinary team.
Department DM - PRODUCT COMMUNICATIONS (1)
Position Location US - Princeton, NJ
City Princeton, NJ
State/Provinces US - NJ
Degree Required Bachelor's Degree Required
Percent Travel 10 - 20%

BUDGET SUPPORT SPECIALIST - PORTFOLIO MARKETING Job (Princeton, NJ, US)

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Requisition ID 17344BR
Title BUDGET SUPPORT SPECIALIST - PORTFOLIO MARKETING
Job Category Marketing
Job Description PURPOSE:
Reports into the Senior Director of Portfolio Strategy and Execution. Supports the functional objectives of the Portfolio Strategy and Execution Team by performing a variety of complex activities of a responsible nature in support of the functional processes, programs, and/or services.

RELATIONSHIPS:
Extensive inter and intra-departmental contact is required as well as contact with individuals representing outside organizations; may research complex or sensitive issues for customers; may provide information on products that directly impact buying decisions. May provide guidance and assistance to lower level clerical positions.

ESSENTIAL FUNCTIONS:
• Coordinates multiple processes, procedures, or programs. Independently researches and develops reports and budgets, draws conclusions, and makes recommendations.
• Demonstrates competencies in the technical, regulatory, legal, or other terminology specific to the appropriate functional processes, as well as a thorough knowledge of department and organization policies and procedures in assigned area of responsibility.
• May be responsible for assisting with the preparation and distribution of clinical documents; budget planning and tracking; providing support of clinical trial activities; assisting with electronic publishing and storage of clinical documents, as well as providing support for timely regulatory submissions.
• May perform a variety of complex activities in support of finance, such as assisting in the monthly close process, account analysis, and reconciliations. May ensure compliance for expense reports by performing targeted audits and providing employee training. May have responsibility for providing IT support for in-house IT clients via phone, email, or intranet requests.
• May perform a variety of complex purchasing, procurement, or pricing duties; manage rebate payments and reporting, provide high quality customer service to patients, pharmacists and health care professionals regarding our products and services, and have responsibility for project management activities.
• May perform duties similar to that of the Business Support Coordinator, in addition to performing a variety of complex activities in support of the functional objectives of assigned department or team, such as Human Resources, Finance, Sales/Marketing, Purchasing, Legal, or Medical/Clinical.
• May provide high level technical and administrative support to Payroll, Fleet, Compensation, Benefits, or other HR functions. May coordinate the training process for field sales personnel. May provide support in the areas of mail distribution, facilities, and equipment.
• Uses software and new/emerging technologies in performing the duties of the position to compile and generate reports, statistics, timelines, tables, graphs, correspondence, and presentations.
• Works independently on a variety of complex and diversified department activities and projects, requiring sound planning, judgment, adaptability, and accountability.
• Works under limited supervision, exercising independent discretion and judgment, where input to changes in work processes and work flow is often required.

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS:
• A high school diploma and 6-8 years of administrative or related experience required.
• Senior level position requiring extensive knowledge of the job and department served; complete knowledge of Company operations.
• Must possess demonstrated skills in PC applications, typically involving new/emerging technologies, such as on-line databases, optical technology, intranet/internet, and computer software programs specific to the function.
• Demonstrated competencies in the technical, regulatory, and legal terminology of the functional processes.
Department DM - PORTFOLIO STRATEGY & EXECUTION
Position Location US - Princeton, NJ
City Princeton, NJ
State/Provinces US - NJ
Degree Required High School Education Required
Percent Travel None

Lead Clinical Research Associate (CRA) Job (Princeton, NJ, US)

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Requisition ID 17457BR
Title Lead Clinical Research Associate (CRA)
Job Category Clinical
Job Description PURPOSE:
Responsible for the performance of assigned sites in accordance with Good Clinical Practice (GCP), ICH guidelines and federal regulations. Responsible for operational aspects of planning and management of site performance in accordance with departmental productivity expectations. Acts as primary liaison between In-House CRAs, Field Based CRAs and the PM for assigned sites. Close collaboration with other members within Clinical Trial Management (CTM) and with various representatives within CMR.

RELATIONSHIPS:
Reports to an Associate Director/Senior Manager/Manager of Site Management (SM) within CTM. Accountable for actively participating in multiple internal cross-functional teams locally to ensure the effective delivery of assigned project milestones. External relationships are with clinical investigators, Contract Research Organizations (CROs), and other clinical research vendors as needed to support business objectives for the department and/or function.

ESSENTIAL FUNCTIONS:

COORDINATION / COMMUNICATION, ADMINISTRATION AND PERSONNEL DEVELOPMENT:
- Ensure compliance with the application and communication of all Novo Nordisk® policies, procedures and fundamentals.

FUNCTIONAL SUPPORT:
- May participate in continuous improvement processes for function.

PROJECT SUPPORT:
- Accountable for the quality of site performance for assigned sites. Responsible for collaborating with the CRA to develop any Corrective Action Plan (CAP). Accountable for ensuring that the CAP is delivered and issues escalated to the PM in accordance with the CTM escalation pathway. Accountable to assist sites, internal staff and CRAs with the preparation for GCP audits, including file review according to the CTM Audit Management Plan.
- Accountable for providing oversight of the entire site management process for the life cycle of the assigned sites, with the development of essential documents and tracking of site performance metrics.
- Accountable for reviewing and approving all trip reports for assigned sites. Accountable for ensuring that any issues are escalated in accordance with the CTM escalation pathway to the PM.
- Determine and drive the SSV process (track and report progress, review data) ensuring that all sites are selected and supplies provided in accordance with study start expectations.
- Develop and may finalize the country recruitment/retention strategy in collaboration with the Project Manager (PM). Identify potential risks to the enrolment targets based on feasibility analysis in collaboration with the PM.
- Develop Informed Consent (ICF) in accordance with expectations of NNI.
- Develop SSV/SIV and other training tools and training materials in support of the project for the project assigned CRAs.
- Develop study tools for sites and CRA use.
- Ensure that monitoring visits are performed in accordance with protocol/SOP requirements and that these are tracked, including report status and sign off.
- Accountable for the quality of the trip report content and sign off timelines for all assigned sites.
- Facilitate the review of the Monitoring Guideline and ensure that a member of the CRA project team provides input.
- Generate potential site list from key stakeholders across CMR and drive site feasibility process.
- May provide review of eCRF.
- Provide review of protocol and protocol amendments.
- Responsible for the development of any mass site communication as appropriate.
- Responsible to develop and maintain the project Q and A documents.- Responsible to ensure internal productivity metrics, especially for trip report completion within the assigned timeframes and to the expectations of CTM.
- Review and enter all protocol deviations in collaboration with the CRAs.
- Review and provide input to the Trial Materials Manual and ensure distribution to assigned sites and project team members as appropriate (CRAs).

STAFF DEVELOPMENT:
- May provide active mentorship of CTM staff to build talent across the department.
- May develop and maintain guidelines, training programs, policies and procedures for the functional locally.
- May support in the identification of training gaps within function, may support the development of training materials to meet that gap and then provision of training as required to improve core competency and skill set of the department.

TEAM COORDINATION:
- Accountable for the compliance and quality of CATS reporting.
- Active membership to local project teams, contributor to Clinical Team Unit (CTU) Meetings.
- Participates in cross-functional teams, locally, to assure timely attainment of project milestones.
- Responsible for conducting oneself in accordance with expectations as a project team member to ensure the success of a matrix management structure.
- Responsible for ensuring that the mandatory trial entries are made in IMPACT, NovoDOCs, iSITE, EDC administration and updates, and ensure CSIM entries and updates are made.
- Responsible for maintaining focus, locally, for specific project activities within CMR priorities.

TRAINING:
- Attend relevant symposia, conferences and scientific meetings, as necessary
- Provide support and potential identification of training needs across CTM and may support the creation, development and potentially provide training support to meet those needs. This includes any lessons learned sharing across the project team members and/or CTM.

PHYSICAL REQUIREMENTS:
- Approximately 40% overnight travel to visit assigned sites.
- Office based in Princeton, NJ

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS
- A Bachelors’ degree (science-related discipline preferred).
- At least a minimum of 6-8 years of clinical trial experience within pharmaceutical, biotechnology or CRO and/or healthcare setting, of which 4 years must be where the previous roles were directly related to the management of site performance in accordance with clinical trial execution.
- A minimum of 12 months of site monitoring experience required.
- Demonstrated computer skills (MS Office, MS Project, PowerPoint).
- Demonstrates core understanding of medical terminology and clinical trial activities in relation to execution of a clinical development plan.
- Knowledge of GCP as relates to clinical trial management.
Department CMR - SITE MANAGEMENT (4a)
Position Location US - Princeton, NJ
City Princeton
State/Provinces US - NJ
Degree Required Bachelor's Degree Required
Percent Travel 30 - 40%

Associate Manager,Automation Engineering Job (clayton, NC, US)

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Requisition ID 17431BR
Title Associate Manager,Automation Engineering
Job Category Information Technology
Job Description Position Purpose:
Provides leadership and guidance to IT Systems staff responsible for IT and Automation infrastructure, and service and support. Responsible for assisting in developing strategic goals and objectives in alignment with local, DFP, PS and NN business plans. Provides information, feedback and insight to both ITS Manager and site leadership on IT and Automation issues, plans, projects and concerns.

Education: BS/BA in related field

Experience: Min. 6 years IT experience
Min. 4 years supervisory experience

Technical/Process/Functional Knowledge:
Windows Operating Systems
Relational databases (MS SQL, Oracle and Manufacturing Execution Systems (MES))
Automated control systems, related and supporting infrastructure and protocols
Manufacturing information systems
Six Sigma methodologies
Lean manufacturing techniques and methodologies
Proven Process analysis
System development life cycle

Physical Requirements:
Majority of work is performed in a normal office environment Manage relationships with customers, local, corporate management, and external vendors and contractors. Must be able to work flexible hours to support 24/7 manufacturing operation as required.
Department IT Systems
Position Location US - Clayton, NC
City clayton
State/Provinces US - NC
Degree Required Bachelor's Degree Required
Percent Travel 0 - 10%

Sr. QA Area Specialist - Line Filler 36 Job (Clayton, NC, US)

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Requisition ID 17371BR
Title Sr. QA Area Specialist - Line Filler 36
Job Category Quality
Job Description Position Purpose:
Perform compliance and Quality technical review/approvals of protocols/protocol data, specifications, deviations, configuration item lists, etc. Coordinates daily processes and Quality activities for the Line 36 project to ensure objectives are met. Verify systems developed for the L36 project are compliant with applicable regulations and company policies. Perform QA duties on the project and provide input to the project team on compliance. Coordinates with Quality Assurance Aseptic Production (QAAP) and other departments in corrective actions and quality improvement initiatives related to the L36 Project.

Education: Bachelor’s Degree in Life Sciences, Engineering, or related field.

Experience: 6+ years of QA and/or related experience in the pharmaceutical or medical device industry with progressively increasing responsibility.
Demonstrated expertise in Regulations and quality systems (e.g. validation, Change Control, NC/CAPA, Audits, etc.)
Preferred:
Familiarity with local processes and quality systems

Technical/Process/Functional Knowledge:
Audit experience
Demonstrate knowledge of critical controls and input/output requirements for processes in these areas: semi-finished manufacturing and utilities, automation
Expert understanding of validation/system development life cycle approach. Expert in validation concepts with specific competency in Quality Compliance for computer validation
Expert in root cause analysis techniques and cGMP documentation practices. Expert understanding of change control processes.
Expert knowledge of US, EU regulations and guidelines, ISO standards and application of GMPs in aseptic manufacturing. Knowledge of compliance policies and procedures (such as Code of Federal Regulations/21 CFR Part 11).
Excellent written and verbal communication skills.
Basic computer skills in MS Office, MS Project, PowerPoint, etc.
Auditing experience with certification preferred
Mastery of Six Sigma and LEAN tools, cLEAN® 2 star or equivalent

Physical Requirements:
Normal office working environment.
Department Line Filler 36 Project
Position Location US - Clayton, NC
City Clayton
State/Provinces US - NC
Degree Required Bachelor's Degree Required
Percent Travel 20 - 30%

Entry Level Pharmaceutical Sales Representative - Savannah, GA Job (Savannah, GA, US)

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Requisition ID 17051BR
Title Entry Level Pharmaceutical Sales Representative – Savannah, GA
Job Category Sales
Job Description Entry Level Pharmaceutical Sales Representative – Savannah, GA

Novo Nordisk is a focused healthcare company and a world leader in diabetes care. We are actively working to change the course of the diabetes pandemic, improve the daily lives of people with diabetes, and to expand the possibilities for people with hemophilia.

PURPOSE:

The position represents Novo Nordisk to Prescribers within an assigned territory with the goal of maximizing sales and positioning Novo Nordisk as the leading company in diabetes care. Provides an in-house talent pool for future Diabetes Care Specialist (DCS) roles.

RELATIONSHIPS:

Externally, the Diabetes Care Associate (DCA) maintains relationships with physicians, nurses, and other paramedical customers. Internally, the DCA reports to a District Business Manager. The DCA also interacts and collaborates on a regular basis with other field-based employees covering the same geographic areas.

ESSENTIAL FUNCTIONS:

• Actively contribute to the overall sales goals of the Company and its Sales/Marketing Departments by:
o Communicating territory activity through timely submission of monthly highlight reports and other appropriate reports
o Contributing to sales and marketing meetings, training programs, conventions and displays as appropriate
o Partnering with the Novo Nordisk Sales/Marketing Departments to maximize appropriate and effectively use selling materials and product information
o Providing recommendations towards sales and marketing solutions based on understanding and evaluation of trends, dynamics, customer needs, and competitors’ products or services
o Recording notes of calls, including products discussed, key issues and concerns addressed, sales aids utilized, samples distributed, and any other information that will ensure maximum effectiveness for future sales calls
• Develop and maintain a mastery of product knowledge and consultative promotion techniques through:
o Continuously promoting and improving knowledge of Novo Nordisk’s products, competitive products, and sales and promotional skills through participation in company sponsored/approved training programs
o Educating physicians, nurses, and other members of patients’ primary care team on diabetes and the use of Novo Nordisk’s products, including the approved uses and benefits of Novo Nordisk’s products for their patients, related disease states, and the Novo Nordisk brand
o Understanding the most up-to-date clinical studies to educate customers and anticipate questions/concerns about Novo Nordisk’s products
• Coordinating with a manager to effectively prioritize time and available resources to achieve maximum sales in the local territory by:
o Evaluating, identifying, and developing order of calls and routes that maximize the opportunity to call on targeted customers
o Developing and implementing the most effective distribution of product samples in territory
o Ensuring maximum customer penetration and sales volume with limited supervision
o Exercising prudent control over samples and other company property in accordance with company policies and procedures and legal requirements
o Managing a discretionary budget to support sales and additional marketing activities
• Identify, develop, maintain, and leverage relationships with physicians, nurses, and other individuals who make or influence purchasing/prescribing decisions by:
o Analyzing and leveraging an understanding of the patient profiles of targeted and non-targeted physicians in the territory and how those profiles impact territory sales
o Evaluating and determining which stakeholders have greatest opportunity to impact sales and use personalized communication techniques to build and maintain effective relationships with those stakeholders
o Identifying and responding to obstacles to use of Novo Nordisk’s products
o Leveraging an understanding of the impact of managed care on physicians’ prescribing decisions and adjusting sales and marketing strategies accordingly
• Sell and promote Novo Nordisk’s portfolio of diabetes products by:
o Developing a customized approach for each call on each customer to assess customer needs and increase sales of Novo Nordisk’s products
o Utilizing available resources to sell and promote Novo Nordisk’s products, including determining which resources to use in any given situation
o Explaining and promoting features and benefits of Novo Nordisk’s portfolio of products, with an emphasis on which products are best suited for particular patient profiles or circumstances
o Coordinating and implementing medical education activities, programs, and special projects to Impact the local retail market share
o Obtaining maximum commitment from customers on every call
o Listening to customers, including anticipating and responding to customers’ questions, objections, and concerns.
o Determining appropriate messages that reading and react to the customer environment to achieve maximum effect on each sales call
• Learn and stays up-to-date with the “Novo Nordisk Way” of selling

PHYSICAL REQUIREMENTS:

• Approximately 20-40% overnight travel (1-2 days)
• Must maintain a valid driver’s license and obey all applicable traffic laws

DEVELOPMENT OF PEOPLE:

• Not Applicable

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS

• Bachelor degree required
• An aptitude for learning and communicating technical and scientific product and disease information
• Basic computer skills (Excel and Word)
• A valid driver’s license required; willing to travel
• Previous experience in retail, Non-Retail/Inside sales or customer service experience preferred.
• Previous formal leadership role in volunteer/community service, military, or organized athletic team/club preferred.
• Must live within the boundaries of the territory or be willing to relocate
Department SALES - DIABETES SALES
Position Location US - Field Based - Across US
City Savannah
State/Provinces US - GA
Degree Required Bachelor's Degree Required
Percent Travel 30 - 40%

Entry Level Pharmaceutical Sales Representative - STATE COLLEGE, PA Job (State College, PA, US)

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Requisition ID 16796BR
Title Entry Level Pharmaceutical Sales Representative - STATE COLLEGE, PA
Job Category Field Sales
Job Description Entry Level Pharmaceutical sales Representative – State College, PA.

Novo Nordisk is a focused healthcare company and a world leader in diabetes care. We are actively working to change the course of the diabetes pandemic, improve the daily lives of people with diabetes, and to expand the possibilities for people with hemophilia.

PURPOSE:

The position represents Novo Nordisk to Prescribers within an assigned territory with the goal of maximizing sales and positioning Novo Nordisk as the leading company in diabetes care. Provides an in-house talent pool for future Diabetes Care Specialist (DCS) roles.

RELATIONSHIPS:

Externally, the Diabetes Care Associate (DCA) maintains relationships with physicians, nurses, and other paramedical customers. Internally, the DCA reports to a District Business Manager. The DCA also interacts and collaborates on a regular basis with other field-based employees covering the same geographic areas.

ESSENTIAL FUNCTIONS:

• Actively contribute to the overall sales goals of the Company and its Sales/Marketing Departments by:
o Communicating territory activity through timely submission of monthly highlight reports and other appropriate reports
o Contributing to sales and marketing meetings, training programs, conventions and displays as appropriate
o Partnering with the Novo Nordisk Sales/Marketing Departments to maximize appropriate and effectively use selling materials and product information
o Providing recommendations towards sales and marketing solutions based on understanding and evaluation of trends, dynamics, customer needs, and competitors’ products or services
o Recording notes of calls, including products discussed, key issues and concerns addressed, sales aids utilized, samples distributed, and any other information that will ensure maximum effectiveness for future sales calls
• Develop and maintain a mastery of product knowledge and consultative promotion techniques through:
o Continuously promoting and improving knowledge of Novo Nordisk’s products, competitive products, and sales and promotional skills through participation in company sponsored/approved training programs
o Educating physicians, nurses, and other members of patients’ primary care team on diabetes and the use of Novo Nordisk’s products, including the approved uses and benefits of Novo Nordisk’s products for their patients, related disease states, and the Novo Nordisk brand
o Understanding the most up-to-date clinical studies to educate customers and anticipate questions/concerns about Novo Nordisk’s products
• Coordinating with a manager to effectively prioritize time and available resources to achieve maximum sales in the local territory by:
o Evaluating, identifying, and developing order of calls and routes that maximize the opportunity to call on targeted customers
o Developing and implementing the most effective distribution of product samples in territory
o Ensuring maximum customer penetration and sales volume with limited supervision
o Exercising prudent control over samples and other company property in accordance with company policies and procedures and legal requirements
o Managing a discretionary budget to support sales and additional marketing activities
• Identify, develop, maintain, and leverage relationships with physicians, nurses, and other individuals who make or influence purchasing/prescribing decisions by:
o Analyzing and leveraging an understanding of the patient profiles of targeted and non-targeted physicians in the territory and how those profiles impact territory sales
o Evaluating and determining which stakeholders have greatest opportunity to impact sales and use personalized communication techniques to build and maintain effective relationships with those stakeholders
o Identifying and responding to obstacles to use of Novo Nordisk’s products
o Leveraging an understanding of the impact of managed care on physicians’ prescribing decisions and adjusting sales and marketing strategies accordingly
• Sell and promote Novo Nordisk’s portfolio of diabetes products by:
o Developing a customized approach for each call on each customer to assess customer needs and increase sales of Novo Nordisk’s products
o Utilizing available resources to sell and promote Novo Nordisk’s products, including determining which resources to use in any given situation
o Explaining and promoting features and benefits of Novo Nordisk’s portfolio of products, with an emphasis on which products are best suited for particular patient profiles or circumstances
o Coordinating and implementing medical education activities, programs, and special projects to Impact the local retail market share
o Obtaining maximum commitment from customers on every call
o Listening to customers, including anticipating and responding to customers’ questions, objections, and concerns.
o Determining appropriate messages that reading and react to the customer environment to achieve maximum effect on each sales call
• Learn and stays up-to-date with the “Novo Nordisk Way” of selling

PHYSICAL REQUIREMENTS:

• Approximately 20-40% overnight travel (1-2 days)
• Must maintain a valid driver’s license and obey all applicable traffic laws

DEVELOPMENT OF PEOPLE:

• Not Applicable

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS
• Bachelor degree required
• An aptitude for learning and communicating technical and scientific product and disease information
• Basic computer skills (Excel and Word)
• A valid driver’s license required; willing to travel
• Previous experience in retail, Non-Retail/Inside sales or customer service experience preferred.
• Previous formal leadership role in volunteer/community service, military, or organized athletic team/club preferred.
• Must live within the boundaries of the territory or be willing to relocate
Department SALES - STATE COLLEGE, PA
Position Location US - Field Based - Across US
City State College
State/Provinces US - PA
Degree Required Bachelor's Degree Required
Percent Travel 30 - 40%

Entry Level Pharmaceutical sales Representative - Palos Verdes, CA Job (Palos Verdes, CA, US)

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Requisition ID 16992BR
Title Entry Level Pharmaceutical sales Representative – Palos Verdes, CA
Job Category Sales
Job Description Entry Level Pharmaceutical sales Representative – Palos Verdes, CA

Novo Nordisk is a focused healthcare company and a world leader in diabetes care. We are actively working to change the course of the diabetes pandemic, improve the daily lives of people with diabetes, and to expand the possibilities for people with hemophilia.

PURPOSE:

The position represents Novo Nordisk to Prescribers within an assigned territory with the goal of maximizing sales and positioning Novo Nordisk as the leading company in diabetes care. Provides an in-house talent pool for future Diabetes Care Specialist (DCS) roles.

RELATIONSHIPS:

Externally, the Diabetes Care Associate (DCA) maintains relationships with physicians, nurses, and other paramedical customers. Internally, the DCA reports to a District Business Manager. The DCA also interacts and collaborates on a regular basis with other field-based employees covering the same geographic areas.

ESSENTIAL FUNCTIONS:

• Actively contribute to the overall sales goals of the Company and its Sales/Marketing Departments by:
o Communicating territory activity through timely submission of monthly highlight reports and other appropriate reports
o Contributing to sales and marketing meetings, training programs, conventions and displays as appropriate
o Partnering with the Novo Nordisk Sales/Marketing Departments to maximize appropriate and effectively use selling materials and product information
o Providing recommendations towards sales and marketing solutions based on understanding and evaluation of trends, dynamics, customer needs, and competitors’ products or services
o Recording notes of calls, including products discussed, key issues and concerns addressed, sales aids utilized, samples distributed, and any other information that will ensure maximum effectiveness for future sales calls
• Develop and maintain a mastery of product knowledge and consultative promotion techniques through:
o Continuously promoting and improving knowledge of Novo Nordisk’s products, competitive products, and sales and promotional skills through participation in company sponsored/approved training programs
o Educating physicians, nurses, and other members of patients’ primary care team on diabetes and the use of Novo Nordisk’s products, including the approved uses and benefits of Novo Nordisk’s products for their patients, related disease states, and the Novo Nordisk brand
o Understanding the most up-to-date clinical studies to educate customers and anticipate questions/concerns about Novo Nordisk’s products
• Coordinating with a manager to effectively prioritize time and available resources to achieve maximum sales in the local territory by:
o Evaluating, identifying, and developing order of calls and routes that maximize the opportunity to call on targeted customers
o Developing and implementing the most effective distribution of product samples in territory
o Ensuring maximum customer penetration and sales volume with limited supervision
o Exercising prudent control over samples and other company property in accordance with company policies and procedures and legal requirements
o Managing a discretionary budget to support sales and additional marketing activities
• Identify, develop, maintain, and leverage relationships with physicians, nurses, and other individuals who make or influence purchasing/prescribing decisions by:
o Analyzing and leveraging an understanding of the patient profiles of targeted and non-targeted physicians in the territory and how those profiles impact territory sales
o Evaluating and determining which stakeholders have greatest opportunity to impact sales and use personalized communication techniques to build and maintain effective relationships with those stakeholders
o Identifying and responding to obstacles to use of Novo Nordisk’s products
o Leveraging an understanding of the impact of managed care on physicians’ prescribing decisions and adjusting sales and marketing strategies accordingly
• Sell and promote Novo Nordisk’s portfolio of diabetes products by:
o Developing a customized approach for each call on each customer to assess customer needs and increase sales of Novo Nordisk’s products
o Utilizing available resources to sell and promote Novo Nordisk’s products, including determining which resources to use in any given situation
o Explaining and promoting features and benefits of Novo Nordisk’s portfolio of products, with an emphasis on which products are best suited for particular patient profiles or circumstances
o Coordinating and implementing medical education activities, programs, and special projects to Impact the local retail market share
o Obtaining maximum commitment from customers on every call
o Listening to customers, including anticipating and responding to customers’ questions, objections, and concerns.
o Determining appropriate messages that reading and react to the customer environment to achieve maximum effect on each sales call
• Learn and stays up-to-date with the “Novo Nordisk Way” of selling

PHYSICAL REQUIREMENTS:

• Approximately 20-40% overnight travel (1-2 days)
• Must maintain a valid driver’s license and obey all applicable traffic laws

DEVELOPMENT OF PEOPLE:

• Not Applicable

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS
• Bachelor degree required
• An aptitude for learning and communicating technical and scientific product and disease information
• Basic computer skills (Excel and Word)
• A valid driver’s license required; willing to travel
• Previous experience in retail, Non-Retail/Inside sales or customer service experience preferred.
• Previous formal leadership role in volunteer/community service, military, or organized athletic team/club preferred.
• Must live within the boundaries of the territory or be willing to relocate
Department SALES - DIABETES SALES
Position Location US - Field Based - Across US
City Palos Verdes
State/Provinces US - CA
Degree Required Bachelor's Degree Required
Percent Travel 30 - 40%

BRAND DIRECTOR - NOVOLOG Job (Princeton, NJ, US)

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Requisition ID 16881BR
Title BRAND DIRECTOR - NOVOLOG
Job Category Marketing
Job Description PURPOSE:
• Brand Director is accountable for the development and execution of strategic and tactical plans to drive the achievement of Diabetes Brand Marketing business objectives which include: Anchor Budget sales revenue, brand-specific and overall analog market shares (value and volume), TRx, NBRx, value upgrade and non-personal selling initiatives. Oversees and directs all life cycle activities.
• Drives the development of brand strategies and implementation of tactics. Works closely with Marketing Effectiveness to establish, own and defend the brand forecast. Leads the Extended Brand Team (EBT) for designated brand and is responsible for the Brand Plan. Develops key messages and positioning for that brand and proactively communicates with Portfolio Leads and others to ensure transparent communications within and outside the department. Works with Portfolio Leads to create POA “Call to Action” and develops personal and non-personal HCP promotional materials. Ensures brand alignment for all initiatives.
• Incumbent chairs the EBT to ensure execution of plans across the organization.

RELATIONSHIPS:
• Reports to the VP, NovoLog. Manages brand team members and works closely with other internal functional areas including Diabetes Sales, Managed Markets Sales, Managed Markets Strategy & Operations (MMSO), Medical, Commercial Effectiveness (CE), Legal/Government/ Quality (LGQ), and Diabetes Brand Marketing (DBM): Primary Care Professional (PCP), Trade, Institutions and Market Shaping, as well as Global Marketing and Medical colleagues. Other relationships include external vendors/agencies, consultants as well as key opinion leaders and professional organizations.

ESSENTIAL FUNCTIONS:
Fiscal:
• Accountable for the ongoing management and oversight of multi-million dollar brand-specific budget to target levels.
• Ensures budget remains on track.
• Establishes, oversees implementation, and monitors adherence to administrative policies and procedures.
• Evaluates appropriate use and allocation of resources to ensure attainment of unit, department and Company profitability goals.
• Reviews and audits staffs' expense reports.

Product Investment:
• Appropriately seeks human and financial resources to optimize brand within context of overall Diabetes portfolio.
• Develops relationships with and receives commitment from relevant departments and NNAS to ensure the successful execution of strategies.
• Maximizes revenue and profitability and understands return on investment (ROI) concepts to ensure optimization of marketing spend.
• Partners with Marketing Effectiveness to develop and implement marketing metrics. Regularly reviews marketing programs progress to ensure profitability/budget goals are on track. If not meeting metrics, proactively implements corrective measures to increase business impact and overall value.

Promotions:
• Develops and oversees implementation of promotional programs, including coordination with external suppliers.
• Develops and oversees the implementation of marketing plans with promotional budget responsibility.
• Oversees the management of the advertising agency and promotional review board (PRB) process to implement overall campaign elements, educational, promotional and public relations programs.
• Supports the identification, selection and management of professional services to create effective marketing programs to maximize return on investment. This includes symposia, speaker’s programs, print materials, and Phase IV studies.

Strategic Brand Leadership:
• Acts as a key representative of NovoLog product line to outside organizations.
• Demonstrates a strong leadership role across the organization by effectively promoting and engaging in close collaboration with key internal stakeholders.
• Develops and encourages innovative approaches/strategies to maximize brand objectives.
• Develops and oversees implementation of strategic business and related tactical plans.
• Develops and presents compelling plans and strategies for management endorsement.
• Ensures self and team effectively promote/engage in close collaboration with key internal stakeholders (e.g. Diabetes Sales/Medical/Managed Market Sales (MMS) /MMSO/CE).
• Establishes and implements key metrics to track and communicate level of value and impact of brand initiatives to relevant stakeholders.
• Leads the effective integration of various marketing tactics – clinical, medical education, market research and forecasting, advertising, public relations, sales force, patient education, etc.
• Leads the effective planning and coordination with other NNI brands, implementation and quality of all designated marketing strategies and plans. Identifies and implements improvements related to life-cycle activities.
• Leads the NovoLog Extended Brand Team (EBT).
• Provides leadership oversight in ensuring the effective alignment of brand tactics across the various customer segment marketing activities in the Endo and PCP teams to drive business objectives.
• Works closely with Sales Vice Presidents/Regional Business Directors (RBDs), etc. to ensure marketing strategies and programs are developed that strongly support customer needs and are of high impact.
• Works effectively with international colleagues for coordination of the brand strategies and to share best practices, etc.

PHYSICAL REQUIREMENTS:
Approximately 40% overnight domestic and international travel.

DEVELOPMENT OF PEOPLE:
• Ensures that reporting personnel have 3P (Annual Performance Management) forms with annual goals and measurements that are consistent with the priorities of the business, and that interim reviews are held so that their work is focused on those priorities, and they understand their level of accountability for results and the measurement process.
• Ensures that the Individual Development Plan (IDP) forms include completed Learning and Aspiration plans and are in place for all reporting personnel to enable the achievement of goals and capability to assume increased levels of responsibility.
• Leads, directs, motivates, inspires, develops and coaches staff.
• Manages the application and communication of all Novo Nordisk policies, procedures, and Novo Nordisk Way of Management.

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS
• 10 years progressive marketing/brand management and sales experience demonstrating a steady career progression with increasing roles of responsibility within the pharmaceutical industry required.
• A Bachelor’s degree required.
• At least 2 years solid management experience required.
• Demonstrated collaboration skills in leading cross-functional teams required.
• Excellent presentation/communications skills required.
• Proven track record of innovative market shaping accomplishments/high impact results (based on metrics/ROI).
• Solid understanding of the marketplace and competition, preferably within diabetes.
• Strategic Planning, Execution and follow-through skills required.
Department DM - NOVOLOG / NOVOLOG MIX 70/30 (3)
Position Location US - Princeton, NJ
City Princeton, NJ
State/Provinces US - NJ
Degree Required Bachelor's Degree Required
Percent Travel 30 - 40%

Senior Project Manager, Clinical Project Management Job (Princeton, NJ, US)

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Requisition ID 16909BR
Title Senior Project Manager, Clinical Project Management
Job Category Clinical
Job Description PURPOSE:
Responsible for the operational and financial management of clinical trial planning and execution for assigned projects. Close collaboration with other members within Clinical Trial Management (CTM) and with various functional units of NNI as well as HQ. Accountable for performance of assigned staff in project delivery.

RELATIONSHIPS:
Reports to the Associate Director/Director of Portfolio Management within Clinical Trial Management (CTM). Accountable for actively leading internal cross-functional teams locally to ensure the effective delivery of all project milestones. Effectively manages to the direction and strategy for performance within clinical trials at NNI thereby facilitating the CTM department to effectively manage all its business deliverables. Reporting to this position are Project Managers. External relationships are with clinical investigators, Contract Research Organizations (CROs), and other clinical research vendors as needed to support business objectives.

ESSENTIAL FUNCTIONS:
Budget & Contract Coordination:
- Ensuring project budget is developed and managed in line with organizational expectation, including the development of appropriate site budgets.

Coordination/Communication, Administration and Personnel Development:
- Ensure compliance with the application and communication of all Novo Nordisk® policies, procedures and fundamentals within the assigned staff.
- Ensure that all personnel understand and work towards corporate, department and individual goals and that the measures of those goals are understood and accepted.
- Ensure that all personnel understand the priorities of the business, that they are focused on those priorities and that their level of accountability is understood and accepted within a matrix environment.
- Ensure that all personnel understand the priorities of the business, that they are focused on those priorities and that their level of accountability is understood and accepted.
- Responsible for the coaching, development and growth leading directly to improvement of talents of the personnel within the assigned region to meet increasing levels of responsibility.

Departmental Management and Staff Development:
- Active mentorship of CTM staff to build talent across the department.
- Actively follows and manages the application and communication of all Novo Nordisk policies, procedures, and Novo Nordisk Way of self and instill in all staff across CTM department.
- Responsible for ensuring that the IDP forms include completed Learning and Aspiration plans and are in place for all reporting personnel to enable the achievement of goals and capability to assume increased levels of responsibility.

Functional Management Support:
-Implements and may participate in continuous improvement processes for function.

Project Management and Staff Development:
- May support and communicate functional, departmental or organizational initiatives.
- May support the maintenance of guidelines, training programs, policies and procedures for the functional locally. Approves vacation requests, meeting attendance, expense reports and check requests for staff.

Project Management/Support:
- Cross team membership, coordination and motivation of the region across NNI. Lead Clinical Trial Unit (CTU) meetings across CMR. Responsible to represent NNI at International Study Group Meetings with HQ.

Project Management:
- Accountable for all aspects of vendor management for assigned studies, responsible to drive them to complete their activities in accordance with any contracted terms.
- Accountable for all project timelines and deliverables. Evaluates and communicates the probability and impact of risks, develops quality and risk management plans for performance and ensures this is integrated into the overall plan for the monitoring management project deliverables in accordance with project plan.
- Accountable for leading the activities relating to the execution of the CTM Audit Management Plan for assigned studies.
- Accountable for the quality of the clinical trial execution in partnership with CTM Managers and the assigned Lead CRA. Accountable for the development of the study specific quality plan.
- Active leadership to local project teams.
- Development and finalization of the study communication plan.
- Ensure local protocol amendments are written and submitted in a timely manner in accordance with local expectations.
- Facilitate the review of protocols with CTM team members, ensure PRC submission is completed in line with departmental expectations.
- Oversee the development of the eCRF or CRF as appropriate.
- Oversee the feasibility process, development of the feasibility questionnaire through collaboration across CMR key stakeholders. Accountable the final determination of the study site list from the site selection process.
- Oversight of the label approval process.
- Prepare and provide input into materials for Investigator Meetings and Monitors Training Meetings.
- Prepare and work with meeting planning group and HQ to plan and execute the coordination of the Investigator Meetings.
- Responsible to ensure that all data pertaining to study status is compiled and reported monthly as appropriate.

Staff Management and Staff Development:
- Active membership to local management teams.
- Direct supervision of assigned staff, including training, development, hiring, discipline, and terminations for them and the function. Ensures that standardized goals and objectives are implemented on corporate and local BSC targets.
- May support the identification of training gaps within function or assigned personnel, may support the development of training materials to meet that gap and then provision of training as required to improve core competency and skill set of the department or assigned staff.
- May support the maintenance of guidelines, training programs, policies and procedures for the functional locally. Approves vacation requests, meeting attendance, expense reports and check requests for staff.
- Responsible for the implementation and execution of strategies employed by the staff to meet corporate or local goals or directives.
- Responsible to ensure that reporting personnel have 3P forms with annual goals and measurements that are consistent with the priorities of the function, and that interim reviews are held so that their work is focused on those priorities, and they understand their level of accountability for results and the measurement process.

Team Coordination:
- Accountable for the compliance and quality of CATS reporting for assigned personnel.
- May support the implementation cross departmental work, locally, and communications for assigned as per the clinical development plans.
- May support the implementation of work within cross-functional teams, locally, to assure timely attainment of department milestones within CMR.
Additional Information Team Coordination Continued:
- Responsible to ensure that staff are consistently driving and partnering with the project teams to ensure transparency and partnership structure that assures the appropriate updates are provided, that performance is to their expectations and that there clear understanding of expectations as a project team member from the function to ensure to the success of a matrix management structure.
- Responsible to ensure that the mandatory trial entries are made in IMPACT, NovoDOCs, iSITE, EDC administration and updates, and ensure CSIM entries and updates are made.
- Responsible to maintains focus, locally, for specific department activities within CMR priorities.

Training:
- Attend relevant symposia, conferences and scientific meetings, as necessary.
- Provide support to needs across CTM and direct the creation, development and potentially provide training support to meet those needs.

PHYSICAL REQUIREMENTS:
- Approximately 20-40% overnight travel
- Office Based - Princeton, NJ

DEVELOPMENT OF PEOPLE:
- Active mentorship of CTM staff to build talent across the department.
- Approves vacation requests, meeting attendance, expense reports and check requests for staff.
- Direct supervision assigned staff, including training, development, hiring, discipline, and terminations.
- Ensure staff are actively developed in the accordance with the departmental expectations.
- Ensure that reporting personnel have 3P forms with annual goals and measurements that are consistent with the priorities of the business, and that interim reviews are held so that their work is focused on those priorities, and they understand their level of accountability for results and the measurement process.
- Ensure that the IDP forms include completed Learning and Aspiration plans and are in place for all reporting personnel to enable the achievement of goals and capability to assume increased levels of responsibility.
- May develop and maintain guidelines, training programs, policies and procedures for the functional locally.
- May identify training gaps within region/function, may support the development of training materials to meet that gap and then provision of training as required to improve core competency and skill set of the department.
- Provides standardized goals and objectives to the function based on corporate and local BSC targets.

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS
- A Bachelors’ degree required (scientific discipline preferred) .
- A minimum of 10 years of clinical trial experience within pharmaceutical, biotechnology, CRO company and/or healthcare setting, i.e. managing the logistics of clinical trial conduct and developing/executing project plans for clinical development programs.
- A minimum of 12 months on site monitoring or related equivalent experience required.
- A minimum of 2 years of experience in international trial management.
- A minimum of 2 years of supervisory experience preferred.
- Analytical, negotiation, meeting management, cross-functional team and leadership skills required as demonstrated from representation at a management level.
- Demonstrated computer skills (MS Office, MS Project, PowerPoint).
- Demonstrates core understanding of medical terminology and clinical trial activities in relation to execution of a clinical development plan.
- Knowledge of GCP as relates to clinical trial management.
Department CMR - PROJECT MGMT (1d)
Position Location US - Princeton, NJ
City Princeton
State/Provinces US - NJ
Degree Required Bachelor's Degree Required
Percent Travel 20 - 30%

Executive Assistant with lean competences and leadership potential (Hillerød, Denmark)

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Executive Assistant with lean competences and leadership potential

- Research & Development
- Denmark - Hillerød

In this job, 366 million people worldwide will depend on you to support the development of the world’s best medical devices. If you find challenges like this exciting and inspiring, you may be our new Senior LEAN Consultant & Executive Assistant in the Competency Centre, supporting our portfolio of medical device projects.

About the department
Device Research & Development is an area within Global R&D, responsible for the development of medical devices for self-treatment within all business areas of Novo Nordisk A/S. Device Research & Development has a long and outstanding track-record of developing the best, most innovative and widely-used injection devices in the world.

In the Device R&D Competency Centre, we are more than 100 highly skilled employees covering a broad range of specialist areas with deep subject matter expertise supporting the portfolio of Device innovation and development projects. We are responsible for project support, such as prototyping, device testing, computer aided engineering, materials, risk management and packaging for all Novo Nordisk drugs and medical devices.

To read more about Device R&D use this link: www.novonordisk.com/Device-RD

The job
You will report to the VP of Competency Centre and will be part of the Competency Centre Management team, characterised by a high expertise level and profound insight into our business. We focus on improving the value of our offerings and reducing the lead times in device development projects.

Your overall focus will be to identify and conduct improvement projects, with special focus on the interaction between the Competency Centre and the development projects, while optimising the internal processes in the Competency Centre. Together with a team of consultants you will support the management team in the implementation of LEAN leadership.

On a day-to-day basis you will support and challenge the Management Team in achieving ambitious results and securing clear communication both internally and towards our many stakeholders. Furthermore you will be responsible for budget planning and follow-up. You can anticipate a very independent job where you actively contribute to lasting and measurable improvements.

Qualifications
You must have an academic degree, e.g. within engineering or business. Proven track record and experience of implementing improvement projects / LEAN in complex environment are also key. Most likely this experience is gained within a Research & Development organisation, perhaps in the pharmaceutical or medical device industry, but experience could also be gained in other complex industries.

Most important are your personal skills. You are able to communicate organisational and improvement matters to engineering specialists as well as to management. In addition, you come across as data driven with clearly strong analytical skills as well as the ability to think critically and challenge. You must have a high energy level and empathy as well as engagement and a decisive approach. Moreover, you must have a positive mind set and the ability to complete tasks. Career ambitions are welcome and your long term ambitions may include leadership roles.

Device R&D is an organisation with many international employees and we welcome non-local applicants. We have great experience helping people move to Denmark and will support relocation.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same within a global business environment.

Contact
For further information, please contact Lars Stenholt at +45 3079 9856.

Deadline
5 January 2014

Pharma Field Sales -District Business Manager (DBM)Coastal Carolina,NC Job (Wilmington, NC, US)

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Requisition ID 16571BR
Title Pharma Field Sales -District Business Manager (DBM)Coastal Carolina,NC
Job Category Field Sales
Job Description Pharma Field Sales - District Business Manager (DBM)-Coastal Carolina, NC

PURPOSE:
To develop and lead sales teams in the execution of sales strategies that increase profitability to maximize sales objectives. Works with RBD to manage, train, develop staff, and prepare regional budget and business plans. This is an entry level district business manager position.

RELATIONSHIPS:
Reports to the Regional Business Director. Manages a region’s sales force, and has direct supervisory responsibility for Pharmaceutical Sales Representatives. Works closely with RBD, peers and the home office to achieve sales objectives and to ensure the development of people. Other relationships include physicians, key accounts, co-promotion partners, associations, field and home office personnel.

PRINCIPAL ACCOUNTABILITIES:

BUSINESS PLANNING
•Work to develop a full understanding of the content and then execute the regional business plan to achieve the fulfillment of Plan objectives/requirements. This includes delivery-of-care system delineation, account targeting, needs assessment, and program implementation.
•Execute regional level account targeting strategy in business unit to fulfill regional account targeting strategy requirements.
•Manage business unit customer needs assessment. Apply assessment frameworks against accounts in region by overseeing DCS account assessment activities. Identify program/service requirements for addressing needs. Work with the VP Diabetes Sales, Field Sales, Regional Directors and appropriate home office management to feed requirements into program development (contracting, marketing programs).
•Oversee regional account relationship development/management. Manage critical regional account relationships and set account relationship development objectives for regional staff.
•Manage regional resource allocation.
•Monitor regional program/initiative effectiveness.
•Monitor performance against strategic account management objectives/directives.

COORDINATION/PARTNERSHIP
•Ensure contractual requirements are met for the region (# of physician calls per day).
•Work with RBD, DBMs, home office and CSO counterparts to gain insight into programs and initiatives.
•Gain an understanding of regional level coordination between field resources, intra-organization resources and inter-organizational resources. Work with RBD to incorporate district.
•Ensure appropriate level of coordination to attain regional business plan objectives.

ADMINISTRATION
•Communicate Regional activity of competitive products through timely submission of monthly highlight reports as directed.
•Review and audit expense reports.
•Evaluate appropriate use of regional resources to ensure attainment of profitability goals.
•Develop and monitor performance against regional budgets.
•Establish and oversee regional implementation, and monitor adherence to administrative policies and procedures.
•Ensure timely and accurate submission of administrative requirements.

ADHERE TO AND SUPPORT COMPANY POLICIES, PROCEDURES AND SALES/MARKETING DIRECTION. IMPLEMENT COMPANY POLICIES, PROCEDURES AND SALES/MARKETING DIRECTION THROUGHOUT THE RBU
•Monitor and reinforce the use of the Sales Force Automation System.
•Ensure timely and accurate transmission of DCS call data.
•Adhere to the Prescription Drug Marketing Act of 1987 and all related Novo Nordisk policies regarding the judicious use of physician samples and stock items.

DEVELOPMENT OF PEOPLE/MANAGEMENT
•Fill open territories with high quality talent within 6 weeks.
•Ensure that reporting personnel have Performance Achievement Plans with annual goals and measurements that are consistent with the priorities of the business, and that interim reviews are held so that their work is focused on those priorities, and they understand their level of accountability for results and the measurement process.
•Manage the application and communication of all Novo Nordisk policies, procedures, and Novo Nordisk Way of Management.
•Ensure that development and training plans are in place for all reporting personnel to enable the achievement of goals and capability to assume increased levels of responsibility.
ATTAIN AND MAINTAIN PROFICIENT LEVELS OF NNPI AND COMPETITIVE PRODUCT KNOWLEDGE
•Continuously improve the knowledge of Novo Nordisk products, competitive products, and management skills through ongoing home study and participation in company sponsored/approved training programs.

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS:

• At least 5 Years Progressive Pharmaceutical/Healthcare Sales experience required
• 2 Years Previous Supervisory experience preferred
• Bachelor Degree required from College or University accredited by an organization recognized by the US Department of Education; major in Business or Marketing preferred.
• Top 20% sales ranking for 1 out of last 2 years, documented (Regionally)

OTHER:
•Works within NNPI’s established policies and procedures and ensures alignment of their work to Novo Nordisk Fundamentals.
•Minimum of 5 years of progressive pharmaceutical/healthcare sales experience required.
•Significant record of sales accomplishments.
•Two years previous supervisory experience preferred.
Department SALES - COASTAL CAROLINA NC
Position Location US - Field Based - Across US
City Wilmington
State/Provinces US - NC
Degree Required Bachelor's Degree Required
Percent Travel 20 - 30%

Operations Area Specialist 12hr days + every other weekend Job (clayton, NC, US)

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Requisition ID 16735BR
Title Operations Area Specialist 12hr days + every other weekend
Job Category Manufacturing
Job Description Position Purpose:
Serve as key member of shift production leadership team providing operations support and coaching.

Education: BA/BS degree or industry equivalent experience.

Experience: Five (5) years of manufacturing experience in a pharmaceutical environment.
Two (2) years of Aseptic Processing experience (Aseptic Processing Department only).

Technical/Process/Functional Knowledge: Experience using Lean/Six Sigma methodologies and achieving sustainable process improvements. .
Ability to communicate technical information clearly in writing and presentations.
Demonstrates knowledge of adult learning methodologies and is able to use multiple methods to train and coach others.
Computer expertise in the following applications: MS Word, Outlook, Excel, PowerPoint, Access, SAP and novoLIMS

Physical Requirements:
Ability to work 12 hour shifts or longer, day or night.
Ability to attain clean room gowning certification and work with hazardous materials including sanitants. (Aseptic Production)Ability to work hours necessary to support shift production.
Ability to travel internationally
Ability to achieve core gown certification (Aseptic Production)
Department Aseptic Production Team A
Position Location US - Clayton, NC
City clayton
State/Provinces US - NC
Degree Required Bachelor's Degree or equivalent experience
Percent Travel 0 - 10%
Shift Day

HPLC QC Chemist with extensive GMP experience (Gentofte, Denmark)

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HPLC QC Chemist with extensive GMP experience

- Quality
- Denmark - Gentofte

Do you want to be a part of a team in growth? Are you customer orientated and do you want to ensure the right quality of analysis in Biopharm? Then you might be our new colleague for a two year temporary position.

About the department
Biopharm QC Chemistry performs chemical and biological analysis on finished products, API, and handles stability studies and customer complaints, covering several biopharmaceutical products.

The department consists of about 80 dedicated employees divided into four teams. We have a busy and stimulating working environment with lots of opportunities to develop both your professional and personal competencies. The position is placed in one of our two HPLC teams. Today the HPLC team consists of 10 laboratory technicians, 5 chemists and 1 Associate Manager. The main responsibilities for the team are HPLC and GC analysis on Norditropin and Glucagon.

The Job
As a QC Chemist you will be one of the key players in securing compliance and you will be a part of the daily operation from analysis to result release on product. You have to be able to evaluate and solve challenges via your scientific skills and your solid knowledge within GMP compliance. It is important that you can handle several tasks at ones and be able to finish them timely. Typical daily tasks could be release of analytical results, handling of non-conformities, laboratory investigations and change requests as well as many different types of compliance projects.

Qualifications
You have an academic degree (Cand. Pharm, chemical engineer, biochemist, or other equivalent level of education) and you have several years of experience with GMP and the requirements of the authorities in the pharmaceutical industry.

You have experience working with HPLC and you are familiar with qualification of equipment and validation. You are experienced with Lean and one of your strengths is your analytic ability to perform systematic troubleshooting. You are fluent in Danish and English both spoken and written and you have flair for preparing documentation. You possess good communication skills and will be able to present documentation at inspections.

Contact
You have a strong quality mind-set. You are open minded and engaged and you are capable of motivating and inspiring your colleagues. You keep a sense of perspective and high spirits in a busy working environment. You work in a structured and systematic way and are used to deliver according to targets.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth

Contact
For further information please contact Anders W. Nielsen on +45 3075 9440.

Deadline
05 January 2014.

Director, Health Economics & Outcomes Research-Strat & Research Collab Job (Princeton, NJ, US)

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Requisition ID 16587BR
Title Director, Health Economics & Outcomes Research-Strat & Research Collab
Job Category Medical Information
Job Description PURPOSE:

Position is responsible for contributing to the development and implementation of Health Economics and Outcomes Research (HEOR) related strategies and tactics across the Diabetes and Biopharm portfolios. The incumbent develops strategies and tactics for strategic research collaboration partnerships with appropriate customers, and development of strategy regarding Comparatives Effectiveness Research (CER) initiatives and related policy. S/he provides HEOR scientific data, research, and training expertise to support key internal customers in CMR, Government Affairs, Commercial Effectiveness, Marketing, and other appropriate functions. S/he also leads the effort in providing HEOR scientific data, research, and training expertise to support key external customers who are health care policy and/or formulary decision makers in academia, payor, clinical, and regulatory environments.

RELATIONSHIPS:

This position reports to the Senior Director, HEOR, Strategic Development and Analytics. The other key internal relationships include Medical Affairs, Managed Markets Sales, and Managed Markets Strategy, Government Affairs, and Commercial Effectiveness personnel. External relationships include key national and regional payers including (Managed care organizations, federal and non-federal institutions, long-term care, influential academic health economic or health policy key opinion leaders (KOL’s) and other key formulary influencers (KFI’s).

ESSENTIAL FUNCTIONS:

ADMINISTRATIVE DUTIES:

• Develop and manage budget for HEOR research collaboration partnerships and HEOR data field dissemination
• Effectively manage assigned HEOR projects
• Provide monthly report on assigned HEOR activities to manager
• Ensure that all required NNI training is completed in a timely manner to ensure compliance.
.
HEOR ADVOCACY DEVELOPMENT:

• Develop strategy and serves as a champion for NNI HEOR research collaborations with appropriate costumers by actively identifying and developing research relations with key HEOR/CER decision makers in health-care, health-policy, academia, and other related settings in order to support the NNI portfolio and expand NNI knowledge and influence in external HEOR/CER related trends and policy development
• Attend assigned meetings and symposia to maintain up-to-date knowledge of current issues and new data pertaining to NNI products and disease areas
• Maintain a thorough and detailed working knowledge of products within the NNI portfolio, as well as current scientific, health economic, and health policy research in order to be regarded as a subject matter expert in HEOR/CER trends and policy to both internal and external stakeholders
• Be a strong partner with key internal stakeholders within Managed Markets Sales and Medical Scientific Affairs to identify HEOR/CER specific scientific support needs at key MMS accounts
• Partner with HEOR team leaders in the development of appropriate HEOR research to support NNI brand strategies and tactics.

HEOR RESEARCH

• Takes a leading role in establishment of strategic research partnerships with appropriate external entities; including identification and evaluation of potential partners, contracting, development and participation in research projects, and communication of results within established NNI guidelines. Accountable for day to day management of field research projects using Real World Data.
• Provides clinical and health systems expertise to internal stakeholders for HEOR research conducted using the One NN Databases as appropriate.
• Participates in the coordination of appropriate communication of research results via the development of abstract/poster/manuscripts in collaboration with NNI internal stakeholders and Publication Planning as required.

HEOR COMMUNICATION AND TRAINING

• Works closely with HEOR group leaders and develop strategy for HEOR data field dissemination
• Presents results of HEOR research projects to external stakeholders using appropriate tools in accordance with appropriate NNI policies.
• Presents results of HEOR research projects to internal stakeholders in CMR, Marketing, and other appropriate functions using appropriate tools in accordance with appropriate NNI policies and SOPs.
• Takes lead in development appropriate tools and deliverables; including slide decks, to communicate results of HEOR research projects to appropriate internal and external stakeholders in accordance with NNI policies and SOPs.
• Takes lead for the development of and participates in the training with HEOR deliverables for both NNI Field Medical Employees and Field Sales Employees at POA, Pre-POA, FME meetings etc., in collaboration key internal stakeholders, as appropriate.
• Establish role of primary HEOR contact for internal stakeholders in Diabetes and Biopharm commercial and medical field functions; including Managed Markets Account Executives and Field Medical Liaisons.
• Assist with the development and delivery of presentations at HEOR scientific and payer advisory board meetings.

TRAVEL - 30 %

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS

• A PhD Preferred or Masters degree in appropriate field required (heath economics, epidemiology, outcomes research, public health, business/health services research, biostatistics). A PharmD is plus.
• At least seven years of experience in Managed Care, academia, health technology assessment, healthcare industry, or pharmacy practice.
• Demonstrable record of peer-reviewed scientific publications and strategic, customer-focused HEOR tool development helpful.
• Demonstrated experience in working within cross-functional teams.
• Experience in diabetes, growth hormone, or hemophilia therapeutic areas is a plus.
• Experience in HEOR or CER research required.
• Advanced knowledge and experience of health care systems in the U.S., including managed care organizations, PBMs, Medicare, and Medicaid.
• Proven record of outstanding written and verbal communication and negotiation skills, with experience interacting with and presenting to various stakeholders.
• Strong quantitative and analytical skills.
• Strong relationship management skills.
Department CMR - HEOR (1)
Position Location US - Princeton, NJ
City Princeton
State/Provinces US - NJ
Degree Required Master's Degree Required
Percent Travel 20 - 30%

Director - Hemostasis Job (Princeton, NJ, US)

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Requisition ID 16549BR
Title Director - Hemostasis
Job Category Medical
Job Description PURPOSE:
Within Clinical Development & Medical Affairs, Biopharmaceuticals, this Director functions as a
clinical/medical advisor for NNI and key external customers to further scientific exchange. Incumbent provides product and field scientific support to Clinical, Medical and Marketing by using academic credentials and scientific expertise to communicate with health care providers and organizations. The Director will also provide leadership and direction for the conduct and reporting of ongoing local Phase I-IV clinical trials. The Director will provide support to Medical Information, Marketing and Regulatory Departments as needed and will be responsible for overseeing the publication of data and review articles in the hemostasis therapeutic area. The Director will also play a major role in the establishment and function of expert advisory panels in the areas of hemostasis and hemophilia. In addition, the Director will work with and influence medical and scientific aspects of global clinical development projects.

RELATIONSHIPS:
Position reports to the Executive Director, Hemophilia. The Director will work closely with Headquarters, the Clinical Trial Management organization, Medical Writing department, The Regulatory Affairs department and Medical Affairs and Marketing organizations Additional key internal relationships are with the regional medical liaisons and directors, research clinicians and clinical project managers, marketing, MCT&G, and Sales personnel. External relationships include key opinion leaders (KOL’s), academic institutions, managed care organizations, physicians, nurse practitioners, and pharmacists.

ESSENTIAL FUNCTIONS:
- Provide monthly (or more frequent, when required) report on all activities to Executive Director
- Identify, contact, develop and maintain relations with health care providers to establish and/or support the use of NNI products; when necessary, assist in resolving issues pertaining to that use.
- Responsible for establishing and coordinating the scientific activities of consultant and advisory boards.
- Maintain a thorough working knowledge of NNI, its products, current scientific research and publications associated with same. Provide medical review for hemophilia related promotional materials.
- Provides leadership for scientific support activities and supports CTO personnel as needed.
- Provides support to Medical Affairs, conduct needs assessment for therapeutics in healthcare, the risks of intervention and the potential market for intervention.
- Scientific support for marketed products and development projects focusing on NovoSeven® in the hemophilia/congenital bleeding disorder area.
- Support the drug information unit, by providing timely review of materials developed for communication with customers, as well as responding to inquiries where specific professional expertise in hemostasis/hemophilia clinical science is required.
- Works with the Executive Director, Hemostasis, the Director, Marketing and the Project Manager(s) to identify scientific needs and research opportunities and implements tactics to support scientific and business needs in the U.S.
-Assist in the development of timelines, and budgets, relevant to the management of ongoing local trials and registries.
- Ensure timely publication of clinical trial results.
- Helps to support and analyze clinical trial and registry data relating to Phase I-IV studies.
- Identify academic centers and investigators to initiate and/or participate in clinical trials and identify key areas of future research.
- Obtain expert medical community input as required to design high quality studies.
- Provide regional medical input on the global clinical development plans related to hemophilia.
- Serve as an advisor to clinical research teams for projects in early stage development.
- Write, review, and/or approve and ensure quality Phase I-IV clinical trial protocols.
- Assist with training of field personnel on product knowledge and use of technical information in selling situations.
- Design, develop, and deliver scientific presentations to individuals and groups of strategic importance to NNI.

PHYSICAL REQUIREMENTS:
Approximately 30% overnight travel.

KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS
An M.D. degree with completed residency program required, preferably in hematology, critical care or related field.
Clinical trial experience desirable.
Minimum of 5 years’ experience in a pharmaceutical company, preferred hemostasis, hemophilia, bleeding
and clotting disorders experience strongly preferred
Strong strategic mindset, understanding of market needs, resource allocation, etc.
Strong tactical familiarity with the design, overseeing and assessment of clinical trials and with other MA tools
Department CMR - HEMOSTASIS
Position Location US - Princeton, NJ
City Princeton
State/Provinces US - NJ
Degree Required Doctorate Degree Required
Percent Travel 20 - 30%

Training Partner - teaching, facilitating & developing (Kalundborg, Denmark)

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Training Partner – teaching, facilitating & developing

Learn more about the largest site in Novo Nordisk�s global production network using this link www.novonordisk.com/kalundborg-careers

- Human Resources
- Denmark - Kalundborg

Do you have experience in developing and implementing training in a production environment, do you have solid project management skills and are you a strong communicator who thrives in being involved with many stakeholders? Then you might be one of our three new Training Partners in Site Denmark

About the department
The Training department service our production sites in Denmark with development and implementation of standards for and documentation of training and consist of 19 employees. We are part of the production of insulin in Product Supply/Novo Nordisk.

The Job
As Training Partner your main role will be to support the implementation of our Operational Training Standard on our productions sites in Kalundborg, Hillerød and Bagsværd with approximately 1.250 employees.

You will primarily spend your time on the production floor in Kalundborg and the job entails a great deal of variation such as project management responsibility, teaching and facilitation at workshops as well as supporting the development of training roles and responsibilities across our sites.

You will be responsible for training various employees in the standard tools and methods we use, while relating the training standard to the employee’s context. You will be an advocate for and communicate the training system to the organisation as well as supporting the organisation to effectively perform training and learning related processes as well as ensuring sustainability going forward.Finally you will organise, develop and coach site training staff and contribute to continuous improvement of our training standards.

Qualifications
You hold a relevant MSc. or MA e.g. within psychology, communication, education or training. It is absolutely essential that you are an excellent trainer and coach and able to set a clear direction. You are able to drive processes proactively in a complex production environment with many stakeholders and you enjoy building relations across organisational areas and levels.Experience with change management processes as well as project management is a prerequisite.

Based on your experience in handling high complexity you are able to prioritise and deliver results without compromising the overall focus and priorities across the organisation.

Your personal qualities define you as robust and a self-starter with a high level of energy. You can safely navigate in an environment of change and are able to establish relations to and cooperate with a wide variety of colleagues. You are driven to achieve results in close interaction with others and are able to take the lead but also to gather others for a common goal is equally important. As a person you have a contagious energy and humour.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information please contact Benjamin Risum at +45 3079 2298.

Deadline
5 January 2014.
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