stillingsbetegnelse: Clinical trial Administrator

jobbeskrivelse:
- Administrative - Denmark - Søborg Being part of Novo Nordisk Research & Development means working at one of the world's largest and most successful biopharmaceutical companies. Our R&D organisation is vital to Novo Nordisk's continued growth and we always welcome talented people who would like to grow with us. If you are motivated by supporting the planning and execution of clinical trials within quality-, timeline- and budget deliverables, you may be our new Clinical Trial Administrator (CTA) in Haemophilia, Clinical Operations. About the department Haemophilia, Clinical Operations is a team of 70 highly skilled and ambitious colleagues responsible for planning and execution of clinical trial activities, hereby securing Novo Nordisk a world leading position within the treatment of haemophilia and rare bleeding disorders. The scope of our activities is phase 1 to 4 clinical trials in collaboration with our Novo Nordisk affiliates. Being a headquarter division our environment is characterised by a vast global network with high quality standards, challenging assignments and continuous career opportunities. The Job Each clinical trial must be conducted according to agreed targets for time and cost and to excellent quality standards in order to ensure approval of the drug. The CTA supports this goal and has a significant role in trial planning and execution by supporting the International Trial Managers with trial related tasks in a proactive and independent manner. The CTA acts as a coordinator for the study team, including coordination of trial activities in collaboration with colleagues at Novo Nordisk affiliates worldwide. Further, the CTA establishes trial master files according to Novo Nordisk Standard Operational Procedures, prepares and maintains trial documents and files. The CTA compiles, archives, creates and imports documents in an internal electronic archive, carries out quality checks and finalises documents. The CTA also supports the study team in meeting planning, execution, and taking meeting minutes. The responsibilities also include preparation and updates of the trial budgets in collaboration with the International Trial Managers. The CTA coordinates trial newsletters and maintains websites as applicable, and finally updates trial information in relevant clinical IT systems (e.g. IMPACT), and prepares trial updates to management. Qualifications Your educational background could include a bachelor degree, preferably within IT or science, with at least two years of experience with similar tasks in the medical/pharmaceutical industry. Fluent in written and spoken English. Team oriented personality with high degree of flexibility and cross-cultural awareness, good communication skills, systematic with attention to details, responsible, preferably a good understanding of project management. Ability and willingness to adjust quickly to new situations in a continuously developing environment. Experienced user of Microsoft Office Package (Outlook, Word, Excel, PowerPoint), preferably with a general flair for IT systems. At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and more than 371 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference. Contact For further information, please contact Karolina Rask at +45 3079 2670 or Nis Hjortskov Jensen at +45 3079 7857. Deadline 25 October 2014.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Job kort beskrivelse: Softwareudvikling

land: Danmark

region: Hovedstaden

Kontrakt varighed: Fast

Kontrakttype: Fuldtid

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark