stillingsbetegnelse: Clinical Trial Administrator

jobbeskrivelse:
- Administrative - Denmark - Søborg Do you want to assist a dedicated team within Global Development? Clinical Pharmacology is looking for a Clinical Trial Administrator to join us. In this job you will be offered exciting opportunities in an international setting and you will be interacting with many colleagues from different parts of the organisation. 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 Clinical Pharmacology is part of Global Development and our main responsibility is planning, execution, and reporting of clinical pharmacology trials within the areas of diabetes, obesity, haemophilia and growth disturbances. The position is based in Søborg, Denmark. The job As Clinical Trial Administrator, you will be responsible for providing assistance to the Clinical Pharmacology Scientist (CPS) in all relevant aspects of trial preparation, trial conduct, documentation, and archiving. You will be responsible for setting-up and maintaining the trial master file, and you will be involved in the preparation of monitoring guidelines, laboratory manuals, enrolment updates, trial budgets, IMPACT updates, handling of contracts, update of clinical documents such as protocol and protocol amendments and ensure electronic filing of documents, all in close collaboration with the trial responsible Clinical Pharmacology Scientist. In addition you will support meeting planning, help with document submissions, and you will be collaborating with a wide range of internal and external stakeholders. Qualifications You have an education as Registered Nurse, Laboratory Technician, or similar, and are experienced in the planning and execution of clinical trials. You are reliable, loyal and service-minded. You have a can-do attitude, enjoy working according to tight deadlines, and possess good coordination skills. You have solid IT skills and work in a structured manner with a sense for the details. It is essential that you can act independently, but also as a team player who thrives on contributing to any team you are part of. You have the ability and willingness to adjust quickly to new situations in a continuously developing environment. You are proficient in both written and spoken English. 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 Birgitte Damholt at +45 3079 4749. Deadline 6 December 2015.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse:
Teknikerarbejde inden for kemisk og fysisk videnskab

land: Danmark

region: Hovedstaden

Kontrakt varighed: Fast

Kontrakttype: Fuldtid

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark