stillingsbetegnelse: Senior GCP Advisor with interest in Quality

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. 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. Do you wish to work in a highly professional, engaged and global environment where you can use your solid GCP knowledge, process optimisation skills and a quality mindset bringing clinical projects to registration and market? You may be one of our new GCP Advisors. In Global Development, we take responsibility for new products based on proteins and peptides from early development phases to product introduction. We are responsible for managing clinical drug development worldwide, securing 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 Global Clinical Compliance department in R&D Quality is expanding and thus seeking a GCP Advisor. The job offers exciting challenges in developing and maintaining our quality management system, with a strong focus on GCP and compliance globally. The department is divided into two teams. The open position is located in the GCC Quality Support Team. The job You will be responsible together with 8 colleagues for ensuring that Novo Nordisk maintains one global clinical quality management system in compliance with GCP and other relevant external and internal requirements. You will be involved in cross-departmental working groups, provide advice on GCP and provide training sessions. You will be responsible for compliance surveillance and for communicatíng compliance issues to the organisation. You enjoy to make presentations within your field of expertise and is good at conveying a message. Qualifications You have a degree in pharmacy, medicine, science or similar and a strong command of written and spoken English. You have at least five years’ experience in clinical research and drug development, as well as solid knowledge of GCP and other relevant regulations. Experience with clinical quality assurance, trial management, or monitoring is required. You take a pragmatic approach to problem solving and have strong interpersonal skills. You are organised, detail-oriented and quality-conscious. You are a team player who thrive working across departments in an international organisation. 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 Lisbeth Bonefeld on +45 3075 8096 or Susanne Nørskov on +45 3079 8151. Deadline 10 December 2014.

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