Scientific Affairs Manager
Term: Permanent
Salary: £53,000 - experience dependant
Location: South coast
This is an ideal opportunity to join a growing and respected pharmaceutical company in a varied and challenging position. You will be charged with managing a multi-disciplinary group responsible for Regulatory Affairs, Medical Information, Quality Assurance and Pharmacovigilance.
Duties:
- Manage the multi-disciplinary group.
- Help oversee reorganising of Medical Information and Regulatory Affairs departments top provide a more flexible service.
- Depending on experience, deputise for the Medical Director in case of absence.
Requirements:
- Several years in pharmaceutical industry with experience in one or more of the above areas but an interest in all.
- Ideally experienced in management.
Key words: clinical pharmaceutical biotechnology medical devices CRO clinical trials clinical development pharmacology health medical research drug safety pharmacovigilance GMC QP management manager medical director
We are dedicated to the clinical research industry, offering candidates a unique service including our free \"Pipeline Watch\" career advisory consultation. To find out more call us on 0118 9594990 or email apply@clinicalprofessionals.co.uk
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