GCP Advisor
- Research & Development
- Denmark - Søborg
Do you want to join a team of highly engaged colleagues working with GCP focusing on the clinical non-conformity process and CAPA investigations you may be one of our new GCP Advisors.
About the department
Global Clinical Compliance department in Quality R&D is expanding and thus seeking additional GCP Advisors. 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 Clinical Support Team.
The job
You will be responsible together with 21 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 the handling of the clinical non-conformities, feeding into the CAPA processes and be a key resource for providing GCP advice to the organisation.
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’re 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
26 September 2013.
- Research & Development
- Denmark - Søborg
Do you want to join a team of highly engaged colleagues working with GCP focusing on the clinical non-conformity process and CAPA investigations you may be one of our new GCP Advisors.
About the department
Global Clinical Compliance department in Quality R&D is expanding and thus seeking additional GCP Advisors. 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 Clinical Support Team.
The job
You will be responsible together with 21 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 the handling of the clinical non-conformities, feeding into the CAPA processes and be a key resource for providing GCP advice to the organisation.
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’re 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
26 September 2013.