2603 International Trial Manager

• R&D-Clinical Development
• Denmark - Søborg
• Date posted: 23 Mar 2010
• Deadline: 6 Apr 2010

Do you want to be part of a dynamic team that drives the trial activities through a fast track development path within our future GLP-1 project portfolio?

Clinical Operations GIC, Future GLP-1 is looking for 3 International Trial Managers to join us. GIC is a combination of a basal insulin and a GLP-1 analogue that is being developed for treatment of type 2 diabetes. This development is supporting our vision of becoming the world’s leading diabetes care company.

By joining us you will be offered exciting opportunities to increase your experience within trial management and develop your competences within a trial life cycle ranging from trial preparation through implementation to trial finalisation.

Challenges
You will function as a global project manager for a single clinical trial with responsibility for the international coordination of trial activities.

You will coordinate trial management activities in a pro-active fashion through clear communication and great team spirit. As chairperson of the international study group you will organise and execute constructive ISG meetings and ensuring the involvement of relevant stakeholders for decision making. You will participate in and contribute to relevant Investigator meetings and monitor meetings.

You will use a structured and analytic approach during protocol development and elaboration of other trial related document such as IC, patient diaries, recruitment strategies, risk analysis plan, communication plans etc.

You sense the important detail through development of specifications to the clinical IT systems set up for the trial, and at the same time you are able to digest complex data output and evaluate the adequate level of quality.

You have the ability to drive the progress of trial activities within given timelines and in accordance with the trial budget that you have prepared and updated.

Our environment is characterised by a vast global network, knowledge sharing and challenging assignments in a dynamic project centric organisation and continuous personal and professional development.

Qualifications
You hold a university degree in medical, biological, pharmaceutical science or equivalent and have broad knowledge of and several years of experience with the execution of clinical trials as well as have a good understanding of project management. You have a quality mindset, meet your deadlines, communicate effectively, and know how to prioritise between different tasks in a dynamic environment. You are a dedicated team player who inspires trust amongst colleagues and partners. You have excellent cross-cultural awareness and like to contribute in multi-cultural project groups. Fluency in written and spoken English is essential.

Contact
For further information, please contact Eva Lysdal Maare, phone +45 3075 1402.

Apply now