Senior Clinical Site Manager

Senior Clinical Site Manager focuses on coordinate priorities, people, activity, budgets, projects, or operational standards according to the role.

What the role involves

• Coordinate priorities, people, activity, budgets, projects, or operational standards according to the role.
• Track progress, solve delivery issues, and communicate clearly with relevant stakeholders.

Skills and requirements

• Minimum of 2-3 years of clinical trial site management experience, ideally in an imaging Clinical Research Organisation or Core Imaging Lab.
• Experience of clinical study site qualification and management for pharaceutical studies, e.g. site qualification, site training.
• Maintain key stakeholder relationships, both internally and externally.
• Experience working within a Quality Management System (QMS), e.g., ISO 9001, ISO 13485 is desirable.

Confirmed role details

• A comprehensive benefits package that includes an annual bonus plan, private medical insurance, life insurance, and a contributory pension scheme.
• 25 days annual leave, plus bank holidays and enhanced maternity leave.

Candidate fit

• site awareness, safe leadership, organisation, and practical decision-making

Additional role context

• Lead site qualification activities for a number of concurrent clinical studies.
• Conduct Qureight site qualification activities for designated, including site evaluation, training and scanner qualification, to ensure timely onboarding of priority clinical study.
• Support and have oversight of more junior team members, providing mentorship and guidance in clinical study site qualification and management.