stillingsbetegnelse: International Trial Manager

jobbeskrivelse:
- Clinical Trial Management - Denmark - Søborg Do you want to be driver of global clinical trials in the Insulin and Diabetes Outcomes project? In Clinical Operations, Insulin & Diabetes Outcomes, we are looking for a new colleague to join us working as International Trial Manager. About the department Clinical Operations, Insulin and Diabetes Outcomes consist of four departments with experienced and enthusiastic Clinical Trial Administrators, International Trial Managers and Clinical Project Managers. Together, as well as in close collaboration with Novo Nordisk affiliates all over the world, we are responsible for planning and conducting clinical trials within the diabetes area from phase 2-4. The Insulin & Diabetes Outcomes 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. Our working environment is characterised by exciting new challenges, a global network, knowledge sharing and continuous professional and personal development which comes when working for a large headquarter function. The job As International Trial Manager you will be responsible for timely planning, execution and finalisation of clinical trials, using your operational and therapeutic expertice. 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 team work. You will organise and execute team meetings as well as planning, preparing and presenting at global Investigator and Monitor meetings. You have a high quality mindset and use a structured and analytic approach when developing trial documents such as protocols, monitoring guidelines, recruitment and retention strategies, risk management plans, communication plans etc. You sense the importance of details when setting up the trial and providing input to clinical IT systems, and at the same time you are able to digest complex data output and evaluate the level of data quality during the trial. You have experience with and proven track record of your ability to drive the progress of trial activities within given timelines and in accordance with the trial budget prepared by you. Qualifications You hold a university degree in medical, biological, pharmaceutical science or equivalent and have broad knowledge and experience with execution of clinical trials and a good understanding of project management. You have a high quality mindset, meet your deadlines, good communication skills, and know how to prioritise between different tasks in a dynamic environment. You are a dedicated team player who inspires trust amongst colleagues and good teamspirit. You have excellent cross-cultural awareness and like to contribute in multi-cultural project groups. Fluency 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 Line Elmøe Glesner on +45 3075 1950. Deadline 11 January 2016.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse: Farmaceutarbejde

land: Danmark

region: Hovedstaden

Kontrakt varighed: Fast

Kontrakttype: Fuldtid

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark