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Team Leader, DM Standards & Support (Søborg, Denmark)

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Team Leader, DM Standards & Support

- Research & Development
- Denmark - Søborg

Are you interested in working in an international and challenging environment where you can use your managerial and technical skills? We are looking for a new Team Leader for our team of CDW Mappers within the Data Management Standards & Support department. We are part of the Global Development organisation responsible for transforming promising new drug candidates into effective treatments for patients.

About the department
The department is situated in Søborg and currently employs 22 people working in various roles to support standard ways of handling data across Novo Nordisk clinical trials. You will be part of a team that supports the use and governance of our clinical data standards across multiple systems used for data collection and reporting of our clinical trials. We are currently in the process of implementing CDISC standards and redefining processes to ensure future compliance. We work closely with multi-functional and international teams on a variety of clinical and technical projects in a pleasant and informal atmosphere.

The job
As Team Leader you will be responsible for day to day management of our CDW Mapper team, whose primary focus is ensuring standardised transfer of data to Novo Nordisk’s custom-built Clinical Data Warehouse (CDW), including mapping of data from CDMS (Oracle Clinical) to CDW for individual trials. You will provide leadership, direction, and prioritisation for CDW Mappers. You will work closely with the Manager of Data Management Standards & Support and the Team Leader for the Global Librarian team, as well as the Manager and Team Leader heading up CDW Mappers at our Global Service Center in Bangalore, India. You will coach, mentor and develop the team in alignment with business needs and Novo Nordisk Way.

Qualifications
You have a strong understanding of the clinical development process within the pharmaceutical industry and a flair for project management and IT. You understand relational databases and regulatory requirements that apply to data collected in clinical trials. Your experience is backed by a degree in a technical or Natural Science discipline. You have minimum 3 years of experience with clinical trial conduct and preferably 2 years’ experience with project or line management, preferably including experience working in international and culturally diverse professional teams. Knowledge of CDISC requirements is also an asset.

As a person you are out-going, motivated, enthusiastic, proactive, and independent. You have excellent communication and presentation skills. You are adaptable with a flexible attitude, both regarding organisation, staff and environment. As a leader, you are able to motivate others, support to the team in meeting new challenges, and lead individuals in a constructive and empathetic manner. We also expect that you are honest, committed, responsible, and well-organised with an efficient and systematic approach.

The position is based in Clinical Systems & Data Management in Søborg, Denmark. Some travelling is expected due to engagement with stakeholders around the world e.g. affiliates and vendors.

At Novo Nordisk, we use our skills, dedication and ambition to help people with diabetes. We offer the chance to be part of a truly global work place, where passion and engagement are met with opportunities for professional and personal development.

Contact
For further information, please contact Heather Brage at +45 3075 0076.

Deadline
8 August 2013.

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