Requisition ID 43151BR<br/>Title Industry Practice Fellowship- Multidisciplinary (PharmD)<br/>Job Category Fellowships<br/>Job Description The Postdoctoral Multidisciplinary Fellowship is a two-year, experiential program based in Plainsboro, New Jersey. This fellowship is intended to provide an experience for Doctor of Pharmacy within the pharmaceutical industry. The postdoctoral fellow will contribute to different functional areas at Novo Nordisk Inc., where a PharmD’s training and expertise will provide value to the organization. The fellow will gain the skills needed to pursue a career within the pharmaceutical industry where their education and experience can make a significant contribution to satisfying customer needs and achieving company goals.<br/><br/>During this one-year fellowship, the fellow will gain experience in three concentrated focus areas: qw months in Medical Information and two 6 months in another functional areas within Novo Nordisk Inc., which may include Global Information & Analysis, Medical Education, Medical Writing or Product Safety Surveillance. The fellow will be selected on a nationally competitive basis.<br/><br/>RELATIONSHIPS:<br/>The fellow will report to their Fellowship Manager/preceptor within Medical Information throughout the 2-year program and will also have a reporting relationship with a manager in the respective functional areas during their rotations. Additional key internal relationships may include CMR Leadership, Medical Affairs, Medical Communications, CMR Training, Clinical Trial Management, Clinical Development, Marketing and Market Shaping.<br/><br/>ESSENTIAL FUNCTIONS:<br/><br/>GENERAL:<br/>* Each fellow will have regular contact with cross functional areas including Medical Operations, Regulatory Affairs, Marketing and Market Shaping, among others. This structured approach will allow for a broad, “hands-on” experience enabling the fellows to gain the skills needed to pursue a career within the pharmaceutical industry.<br/>* All postdoctoral fellows will complete a Fellowship project for presentation at a key conference/congress. Additionally, fellows may be asked to attend other relevant scientific conventions, national team meetings and other travel as required for business needs related to fellow projects as appropriate.<br/>* The following are examples of tasks associated with functional areas. Postdoctoral Multidisciplinary Fellows will gain experience for 12 months in Medical Information and two additional 6-month rotations in one of the functional areas listed below.<br/><br/>MEDICAL INFORMATION:<br/>* Gain an understanding of the role and responsibilities of a Medical Information Scientist in a pharmaceutical industry setting<br/>* Develop the skills needed to provide accurate, fair balanced, and current medical and technical information about Novo Nordisk products to healthcare professionals, consumers, managed care organizations and health systems<br/>* Develop competencies in 1) responding to inquiries in both verbal and written forms, and 2) tailoring the responses to the target audience<br/>* Update or create standard Medical Information letters and perform literature searches to stay abreast of the latest scientific information in relevant areas<br/>* Participate in Medical Information projects or task forces<br/>* Participate in product training for sales representatives and in-house colleagues.<br/>* Be the medical accuracy reviewer as needed for promotional pieces undergoing review by the Promotional Review Board (PRB)<br/><br/>Medical Writing (option):<br/>* Gain an understanding of guidelines for ethical publication practice and reporting of clinical trial data (e.g., ICJME, GPP3, CONSORT)<br/>* Gain exposure to regulatory writing processes<br/>* Provide medical writing support to authors in the development of scientific publications (e.g., abstracts, primary manuscripts, secondary manuscripts) and scientific presentations (e.g., posters and oral presentations)<br/>* Coordinate internal medical review and author review of publications<br/>* Assist medical writing members in the preparation of regulatory documents (e.g., clinical trial reports, clinical summary documents)<br/>* During the development of scientific documents, interact and collaborate with internal and external stakeholders including authors, clinicians, biostatisticians, publication planning group, trial managers, regulatory affairs professionals and medical communications agencies<br/>* Attend relevant meetings, such as publication planning group meetings, authors’ meetings, and project meetings<br/><br/>MEDICAL EDUCATION (option)<br/>* Gain an understanding of industry regulations pertaining to independent medical education and ensure that all programs are funded and executed in compliance with these guidelines<br/>* Participate in the review and evaluation of proposals and grant requests submitted by various medical education companies and accredited providers. Analyze needs assessments, educational objectives and program content in submitted grant requests to ensure alignment with medical education strategy<br/>* Project manage assigned medical education programs to ensure successful implementation of programs within budget<br/>* Provide onsite monitoring of select national or regional programs<br/>* Complete medical accuracy review of live and enduring programs, such as web-based programs, monographs and journal supplements, after their dissemination to intended audiences<br/>* Help draft internal communications to highlight the value of medical education<br/><br/>*<br/>GLOBAL INFORMAITON & ANALYSIS (option):<br/>* Collaborate with cross-functional areas including Medical Affairs, Market Shaping, Marketing, Competitive Intelligence, Medical Writing, Health Economics and Outcomes Research and other Information Research & Management units in the U.S. and globally<br/>* Perform and communicate monthly scientific literature analyses (including competitor publication insights and strategies) to cross-functional teams<br/>* Conduct clinical data and conduct publication gap analyses for planning of scientific communications and integration into strategic planning processes<br/>* Contribute to the development of current and “future state” therapeutic area landscapes and assessments<br/>* Serve as the Information Specialist on research/project teams attending meetings and providing needed research assistance and information support to the teams<br/><br/>PRODUCT SAFETY (option):<br/>* Collaborate with Product Safety case management and functional groups to learn about general pharmacovigilance-related activities<br/>* Gain an understanding of basic FDA/Global Health Authority regulations related to capturing and reporting of safety information<br/>* Collect verbal and written safety information from physicians, investigators, healthcare professionals, consumers and NNI sales and field personnel for post-marketing and clinical trial adverse event reports<br/>* Perform and prioritize data entry and verification of safety data into the required complaint and safety databases based on internal and external timelines<br/>* Identify and submit relevant follow-up queries to obtain additional/missing safety information<br/>* Collaborate with Global Safety, vendors, CROs and relevant NNI departments including Customer Care Center, Medical Information and Clinical Trial Management.<br/><br/>Department CMR - MEDICAL INFORMATION<br/>Position Location US - Princeton, NJ<br/>City Plainsboro<br/>State/Provinces US - NJ
<br/><br/>At Novo Nordisk, we know that driving change on a global level and improving treatment outcomes for people with diabetes and other chronic diseases begins here at home. That's why we make an unmatched commitment to our employees, our families and our communities. That means outstanding rewards, industry-leading training programs, and an environment that supports you to achieve your goals at every level. It's all part of the Novo Nordisk Way. It includes our Vision and our commitment to the Triple Bottom Line principle – helping us find the right balance between compassion and competitiveness
<br/><br/>With a career at Novo Nordisk, you’ll feel a difference right from the start. It’s a sense of inspiration and mobility that comes from a shared belief in driving positive change for people, families, and communities everywhere. Congratulations on taking your first step!
<br/><br/><p class="eeo_desc">Novo Nordisk is committed to equal employment opportunity and providing reasonable accommodations to applicants with physical and/or mental disabilities. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, gender, sex, age, religion, creed, national origin, ancestry, citizenship, marital status, physical or mental disability, medical condition, veteran status, genetic information, or any other characteristic protected by federal, state, or local law.<br/><br/>
Novo Nordisk will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.<br/><br/>
If you are interested in applying for employment with Novo Nordisk and need special assistance or an accommodation to use our website or to apply for a position, please call the U.S. Toll Free number at 1-855-411-5290 or click on the following link to submit your request: <a href="https://www.surveymonkey.com/r/novoaccommodation" target="_blank" title="Accomodation Survey">https://www.surveymonkey.com/r/novoaccommodation</a>. Please note we do not accept applications for employment or employment related solicitations through this site. If you are requesting special assistance, please specify your request by selecting "Yes" in Question 2 on the site. We will not be able to respond to requests unless you specify the need for special assistance or an accommodation in Question 2. Determinations on requests for reasonable accommodation are made on a case-by-case basis.</p>
↧