Vice President of Trial Operations

This is an exciting opportunity for the clinical expert with solid people and stakeholder management skills to make a difference heading an area responsible for clinical trial operations. If you are able to set direction, foster innovation and drive change, then this may be the right job for you.

In Global Development, we are responsible for managing clinical drug development worldwide from early development phases to market approval and life cycle management. We ensure medical and scientific documentation for clinical submissions to authorities while ensuring that the processes live 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
Trial Operations, GLP-1 Diabetes, New Anti Diabetics (NADs) & Complications is part of Global Development and consists of approximately thirty employees. We are responsible for the planning, execution and finalisation of clinical trial activities in phase 2-4 developing new and innovative treatments within the area of diabetes and related complications.

We collaborate closely with other functional areas, vendors and colleagues worldwide. We value an open, trust-based and creative working environment, a great team spirit and a high quality mind-set. Our working environment is characterised by interesting and complex assignments and continuous professional development opportunities.

The position
As Vice President, you will report to the Corporate Project Vice President of GLP-1 Diabetes, NADs & Complications in Global Development and be responsible for providing leadership and direction to the Trial Operations area. As part of the Management team, you will contribute significantly to the clinical development of all projects within the area, to the clinical development strategy and to generating high-level clinical documents for submission of new drug applications worldwide. You will also be responsible for ensuring alignment of better practices by active participation in the respective meeting fora.

Some degree of travel should be expected.

Qualifications
You are an experienced people manager with documented experience in the conduct of clinical trials within the pharmaceutical industry. You hold a relevant academic degree within natural sciences or healthcare. We expect you to have profound experience in the operational aspects of planning and conducting clinical trials and demonstrated ability to apply new and innovative methods.

You have solid leadership and coaching skills, a positive personality, constructive team approach and willingness to manage a diverse group in a project centric organisation. You possess an innovative mind-set and the ability to drive change.

Strategic understanding of drug development in the global regulatory arena will be considered an advantage.

Due to the high degree of interaction with external key opinion leaders, commercial partners and health care authorities, we expect you to be a strong communicator, have highly developed social skills and high professional standards.

Working at Novo Nordisk
At Novo Nordisk Research & Development, you will work with specialists from around the world. Our ambitious teams strive to develop innovative drugs, devices and processes and work towards providing the next generation of care. We offer unique possibilities for personal and professional development, as well as a chance to work alongside the best in the field.

Contact
For further information, please contact Karin Kramer Nielsen at +45 3075 4843.

Deadline
28 February 2018.

We will be screening and interviewing candidates on an ongoing basis.


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Indrykket:23. februar 2018
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