GCP Advisor
- Research & Development
- Denmark - Søborg
Do you want to join a team of highly engaged colleagues working with GCP focusing on GCP inspection coordination, as well as following up on implementation of new requirements in the organisation, then 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 conduct of GCP inspections and reporting to management. Furthermore, you will be involved in ensuring new regulatory requirements are processed through the Clinical Issues Focus Group (CIFG) 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 of 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.
Some travel can be expected.
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 +45 3075 8096, or Susanne Nørskov +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 GCP inspection coordination, as well as following up on implementation of new requirements in the organisation, then 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 conduct of GCP inspections and reporting to management. Furthermore, you will be involved in ensuring new regulatory requirements are processed through the Clinical Issues Focus Group (CIFG) 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 of 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.
Some travel can be expected.
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 +45 3075 8096, or Susanne Nørskov +45 3079 8151.
Deadline
26 September 2013.