Senior Clinical Project Manager

Full Job 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:

• 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.

Key Skills:

• 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

This role requires 2 days a week in Surrey offices

For more information contact or click "Easy Apply".