International Trial Manager

Novo Nordisk A/S

Gladsaxe, 1 stilling

- Drug Development

- Denmark - Søborg





Do you have a passion for planning and driving a large global phase III clinical trial programme? And do you want to exert your influence being part of a new team in the process of being created? Then we may have just the right job for you. Clinical Operations, Semaglutide is looking for International Trial Managers to join us.



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 Clinical Operations, Semaglutide we are approximately 50 highly skilled and ambitious employees and we continue to grow as the use of Semaglutide is being further explored. We are right now establishing a new team for handling a large scale innovative programme within oral treatment for type 2 diabetes.



We are responsible for the planning, execution and finalisation of clinical trial activities and collaborate with external vendors, and our colleagues in the Novo Nordisk affiliates worldwide. We value an open, trust-based and creative working environment, great team spirit and a high quality mind-set. We offer unique opportunities for you to play an important role in our evermore imperative work of bringing new and better treatments to the market.



The job

The job as International Trial Manager demands that you are capable of directing and driving activities within global clinical trials. You will be responsible for ensuring that project key deliverables are met in time, at a high quality and within budget. You will be part of the international study group, where you will contribute to planning and conducting team meetings with focus on stakeholder engagement, knowledge sharing and decision making



The job requires that you apply a structured and analytical approach during development of relevant trial documents such as trial protocol, informed consent, recruitment strategies, risk analysis plans, communication plans and trial budgets. You are detail-oriented, while able to maintain overview, digest complex data and evaluate the adequate level of quality.



Qualifications

You hold an academic degree within life science or healthcare. You have knowledge of clinical trial planning, execution and finalisation with a minimum of 2 years’ experience in managing large clinical trials. You are a clear communicator and can inspire and motivate a team to deliver their best in an ever-changing environment. The job requires proficiency in English. You work independently while also being a dedicated team player and have good cross-cultural awareness skills.



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 Benedikte Lertoft at +45 3079 2893



Deadline

25 October 2015.