stillingsbetegnelse: Senior International Trial Manager

jobbeskrivelse:
- Research & Development - Denmark - Søborg In this job, 300.000 people worldwide depend on you to develop the world’s best bleeding disorder treatments. If you find challenges like this exciting and inspiring, you may be one of our new Senior International Trial Managers 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 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 in collaboration with our 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 Senior International Trial Manager you will be the responsible project manager ensuring timely planning, executing and finalizing of clinical trials using your operational and therapeutic experience. You will coordinate trial management activities in a proactive fashion through clear communication and good team work. As a chairperson of the international study team you will organise and execute team meetings and ensure the involvement of relevant stakeholders for decision making. You will participate in and contribute to relevant Investigators and Monitor meetings. You have a structured and analytical approach during development of critical trial documents like the trial protocol, and at the same time you have an eye for important details while keeping the overview. You are able to digest complex data output and to evaluate the adequate levels of quality in all you do. By joining us you will get the opportunity to further develop your competencies within trial management in an international environment. Qualifications You hold a university degree in medical, biological, pharmaceutical science or equivalent with at least 2-4 years of experience with trial management in an headquarter within the pharmaceutical industry. You have a broad knowledge of clinical trial methodology and you have good presentation, communication and negotiation skills. A quality mind set is a must, together with a focus on meeting deadlines, communicating effectively and knowing how to prioritise between different tasks in a dynamic environment. You are a dedicated team player with a high degree of flexibility and cross-cultural awareness who inspires trust amongst colleagues and partners. 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 Helle Lundholm at +45 3079 4302 or Nis Hjortskov Jensen at +45 3079 7857. Deadline 15 February 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