stillingsbetegnelse: International Trial Manager

jobbeskrivelse:
- Clinical Trial Management - Denmark - Søborg Are you our new colleague? Do you want to be a part of a dynamic team that runs the cardiovascular outcome trial, DEVOTE? Are you also prepared to embrace and tackle constant challenges as part of your work each day? Then we may have just 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. We work in global project teams with focus on delivering viable products that make a difference to patients and ultimately benefit society. About the department ClinOps 1, Insulin & Diabetes Outcomes is one out of four departments in Clinical Operations, Insulin & Diabetes Outcomes. The department consists of a well-established team of 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 two cardiovascular outcome trials within the diabetes area. 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 In the temporary position 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 several years of experience with execution of clinical trials and a good understanding of project management. You have a high 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. You have excellent cross-cultural awareness and like to contribute in multi-cultural project groups. Fluency in written and spoken English is essential. 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 Lisbeth Grinder at +45 3079 5591. Deadline 23 June 2015.

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