stillingsbetegnelse:
Experienced Trial Manager with ability to work in a global setting

jobbeskrivelse:
- Clinical Trial Management - Denmark - Søborg As International Trial Manager, people around the world depend on you to develop the best in class bleeding disorder treatments. If you find such a challenge exciting and inspiring, you may be our new colleague within our Haemophilia project portfolio. 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 Clinical Operations, Haemophilia is a team of 70 highly skilled and ambitious colleagues responsible for the planning and execution of clinical trial activities in accordance with the Product Development Plans within haemophilia and rare bleeding disorders. The scope of our activities is phase 1 to 4 clinical trials and non-interventional studies in collaboration with Novo Nordisk affiliates. Our environment is characterised by a vast global network with challenging assignments in a project centric organisation. We focus on continuous personal and professional development and exciting opportunities which arise when working for a large headquarter function. The job As International Trial manager you will be the project manager for the timely planning, executing, and finalising of clinical trials/non-interventional studies. You will be responsible for the development of the protocol, key contributor to the setup of clinical IT systems, laboratories for the execution of the clinical trials/non-interventional studies. You will in close collaboration with Novo Nordisk affiliates ensure timely recruitment. You are together with the study group responsible for the delivery of the final dataset and the trial documentation. As chairperson of the international study group, you will organise and execute internal meeting. You will participate in and contribute to Investigator and Monitor meetings. Travel days are expected. Qualifications You hold a university degree in medical, biological, pharmaceutical science or equivalent with at least 2 years of experience in trial management related positions. You have a broad knowledge of clinical trial methodology. You have excellent presentation, communication and negotiation skills. You are used to work with stakeholders and have the ability to facilitate decisions with the focus on meeting deadlines. You have a high degree of flexibility and have the ability to prioritise in a dynamic environment. You are structured and analytical using your operational and therapeutic experiences in solving assignments. A quality mind-set with an eye for details is a must. You are a dedicated team player with cross-cultural awareness who inspires trust amongst colleagues and external partners. Fluency in written and spoken English is essential. At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth. Contact For further information, please contact Marianne Willert at +45 3079 3277 or Nis Hjortskov Jensen at +45 3079 7857. Deadline 14 December 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