Novo Nordisk A/S
Gladsaxe, 1 stilling
- Research & Development
- Denmark - Søborg
Would you like to assist a dedicated team within Global Development? Clinical Pharmacology is looking for a Technical Trial Manager to join us. In this job you will be offered exciting opportunities to increase your experience within clinical pharmacology trials and to develop your competencies within a trial life cycle ranging from trial preparation through implementation to trial finalisation.
In Global Development we are responsible for managing clinical drug development worldwide from early development phases to product introduction. We ensure medical and scientific documentation for clinical submissions and authorities while ensuring that the process lives up to uniform global standards, regulations and business ethics. We work in global project teams with focus on delivering viable products that make a difference to patients and ultimately benefit society.
About the department
Clinical Pharmacology is part of Global Development and our main responsibility is planning, execution, and reporting of clinical pharmacology trials within the areas of diabetes, obesity, haemophilia and growth disturbances.
The job
As Technical Trial Manager, you will play a key role in coordinating the trial activities in close collaboration with the trial responsible Clinical Pharmacology Scientist in all relevant aspects of trial preparation, trial conduct, documentation, and archiving. You will be responsible for setting-up and maintaining the trial master file, and you will be involved in the preparation of monitoring guidelines, laboratory manuals, enrolment updates, trial budgets, IMPACT updates, handling of contracts, update of clinical documents such as protocol and protocol amendments and ensure electronic filing of documents. In addition you will support meeting planning, help with document submissions, and you will be collaborating with a wide range of internal and external stakeholders worldwide. The position is based in Søborg, Denmark.
Qualifications
You are at present working with clinical trial management or otherwise experienced in the development process around clinical programmes. A degree within relevant area such as nurse or bachelor of science is preferable. You are reliable, loyal and service-minded. You have a can-do attitude, enjoy working under tight deadlines and master good coordination skills. You have solid IT skills and work in a structured manner with a sense for the details. It is essential that you can act independently, but also as a team player who thrives on contributing to any team you are a part of. You have the ability and willingness to adjust quickly to new situations in a continuously developing environment. Fluency in written and spoken English is essential.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Charlotte Keller at +45 3079 1641.
Deadline
20 December 2015.
