stillingsbetegnelse: Medical Writer

jobbeskrivelse:
- Research & Development - Denmark - Søborg Our growth is your opportunity 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. Clinical Reporting is looking for a medical writer in a 1-year temporary position. You will be offered a challenging job with a significant amount of individual responsibility in an international and dynamic atmosphere. 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 Reporting is the medical writing function at Novo Nordisk and is part of Global Development. We are currently 70+ employees, primarily medical writers and clinical publishers. We are a diverse group with different nationalities and professional backgrounds working together in a pleasant and informal atmosphere. We are responsible for preparing clinical documents for submission to regulatory authorities worldwide as well as abstracts and posters for scientific conferences and manuscripts to scientific journals. The job As a medical writer, your main tasks involve writing of regulatory clinical documents such as clinical trial reports, investigator’s brochures, summary documents and other documents covering interpretation and documentation of clinical data. As we cover all clinical development projects within Novo Nordisk’s different therapy areas, the focus and daily tasks depend on the type of document and the life cycle stage of the project. Planning and coordination of activities in a cross-disciplinary setting is also a central part of the job, and we expect that you are capable of driving the writing process and manage the involved stakeholders. The job is globally oriented and requires close collaboration with colleagues in other skill areas both in Denmark and abroad. All documents are written in English and must comply with internal Novo Nordisk standard operating procedures as well as external guidelines. Qualifications You have a university degree within natural sciences (M.Sc., M.Sc.Pharm. or equivalent) including skills within statistics and scientific research methods. Preferably you have developed your scientific research methods and scientific writing skills by completing a Ph.D. You master written and spoken English at a professional level, and you have a flair for, and a genuine interest in scientific communication. In addition, you should be able to communicate in a reliable, professional and trustworthy manner. You are a strong team player who adapts easily to a changing environment with tight deadlines, and you are good at planning, coordinating, managing stakeholders and reaching consensus. You are thorough, structured and conscientious, and you have a good sense of humour. At Novo Nordisk Research & Development, you will work with dedicated specialists from around the world in a growing organisation. We offer unique opportunities for you to progress in your career and play an important role in our evermore imperative work of bringing new and better treatments to the market. Contact For further information please contact Tine Møller +45 3075 7052 or Mette Pierri Stensler-Thomsen +45 3075 2575. Deadline 15 February 2015.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse: Farmaceutarbejde

land: Danmark

region: Hovedstaden

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark