- To manage the life cycle, from start up to close out conduct of post-authorisation studies and interventional clinical trials in accordance with protocols, both local and international regulations, GxP guidelines and Company SOPs, including management of all appropriate documentation.
- Management and oversight of cross-functional team
- Assist with the management of safety reporting requirements of clinical trials and studies, including implementation and regular review of Risk Minimisation Measures
- Participate in key conferences and Company events, as relevant.
- Management and oversight of cross-functional team for clinical trials and post-authorisation studies.
- Previous experience managing clinical research trials/projects (preferably 3 years).
- A nursing, science or related health professional background is desirable.
- Ability or previous experience managing and developing people.
- Excellent working knowledge of ICH/GCP, ethical and regulatory requirements
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Senior Clinical Project Manager - Surrey, United Kingdom - Leaman Life Sciences
Description
My client are looking for a highly motivated Senior Project Manager to manage the conduct of post-authorisation studies and interventional clinical trials in accordance with protocols, GxP guidelines, applicable local and international regulations, and Company SOPs.
Key Responsibilities:
Key Skills:
This role requires 2 days a week in Surrey offices
For more information contact or click "Easy Apply".
