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International Trial Manager for Global Development Søborg Denmark,  


Posted on : 28 March 2017

Project Description

Requisition ID 45871BR Title International Trial Manager for Global Development Job Category Research & Development Job Description Do you want to be part of a dynamic team that drives clinical trial activities in the Insulin and Devices project? In Trial Operations, Insulin & Devices, we are looking for a new colleague to join us working as International Trial Manager.The Insulin and Devices Project is part of Global Development. 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 departmentTrial Operations, Insulin & Devices, is responsible for the set-up and execution of phase 2-4 clinical trials within our diabetes, device and digital health portfolio. We are a large area of approximately 70 enthusiastic colleagues such as International Trial Managers, Clinical Trial Administrators and Clinical Project Managers divided into 5 departments. Our environment is characterised by a vast global network, knowledge sharing and challenging assignments in a dynamic project centric organisation which offers continuous personal and professional development opportunities.The positionAs International Trial Manager you will be responsible for timely planning, execution and finalisation of clinical trials, using your operational and therapeutic expertise. You will chair or co-chair the International Study Group and ensure coordination of trial management activities in a proactive fashion through clear communication and great teamwork. You will organise and execute project meetings as well as planning, preparing and presenting at global Investigator and Monitor meetings. Through a structured and analytic approach and with a quality mind-set you will develop trial documents such as protocols, risk based monitoring plans, recruitment and retention strategies, risk management plans, communication plans etc.QualificationsYou hold a university degree in Biological, Pharmaceutical or Health Science or equivalent with at least 2 years of experience in trial management related positions. You have a good understanding of project management as well as a broad knowledge of clinical trial methodology.  You have a high quality mind-set, meet your deadlines, have good communication skills both in writing and orally, and know how to prioritise between different tasks in a dynamic environment. You sense the importance of details and structure when setting up a trial or project and providing input to clinical IT systems.You are a dedicated team player with a good sense of humour who inspires trust amongst colleagues and good team spirit. You have excellent cross-cultural awareness and like to contribute in multi-cultural project groups. Finally, you must thrive in an environment where ongoing changes are a part of our business development. Fluency in written and spoken English is essential.Working at Novo NordiskAt 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.   ContactFor further information, please contact Tove K. Stryhn +45 3075 3109. Deadline17 April 2017. State/Provinces Denmark Position Location Denmark - S

Locations

Denmark Søborg

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