International Trial Manager for Trial Operations, Obesity

Clinical Trial Management
Denmark - Søborg
Do you have experience in setting up and running global clinical trials and do you want to be part of a team developing new and better treatments for people with obesity? Do you thrive in working as a Project Manager, motivating and engaging stakeholders to deliver on time? Then we might have the right job for you.

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.

About the department
In Trial Operations, Obesity we are approximately 30 highly skilled and ambitious employees. We are responsible for the planning, execution and finalisation of clinical trial activities in phase 2-4 within the obesity portfolio.

We collaborate closely with other functional areas, Contract Research Organisations and our colleagues worldwide. We value an open, team and trust-based working environment. Our working environment is characterised by interesting and complex assignments and continuous professional development opportunities.

The position
You will be part of the International Study Group and ensure coordination of trial management activities in a proactive way through clear communication and teamwork skills. Organising and executing team meetings as well as planning, preparing and presenting at Global Investigator and monitor meetings are also part of your responsibility.

You have a structured and analytical approach as well as a high quality mind-set when developing trial documents such as protocols, monitoring guidelines, recruitment and retention strategies, risk management plans, communication plans etc.

You sense the importance of detail when setting up a trial and providing input to clinical IT systems. At the same time, you are able to digest complex data output and evaluate the level of data quality during a trial.

You are able to ensure progress of trial activities within given timelines and in accordance with the trial budget.

Qualifications
You hold a university degree in Natural Science or equivalent with experience in trial management as well as clinical trial methodology. You have solid project management/leadership skills and work in an independent manner. You must have the drive and focus to meet challenging deadlines and know how to prioritise between different tasks in a dynamic environment. You are a dedicated team player with a high degree of flexibility and cross-cultural awareness who inspires trust amongst colleagues and partners.

Proficiency in written and spoken English is essential.

Working at Novo Nordisk
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 Louise Høyer at +45 3075 1535.

Deadline
30 April 2017.