Senior Clinical Study Manager — Imaging Trials (Hybrid)

Qureight; Cambridge; Hybrid; GBP 90,000 - 120,000; Full time

Benefits offered by this job

Annual bonus plan

Private medical insurance

Life insurance

Cycle-to-work scheme

Contributory pension scheme

Equity

Job summary

Qureight is seeking a Senior Clinical Study Manager to join our Clinical Operations team. You will lead start-up and ongoing study management activities, acting as the primary contact for customers and internal teams while ensuring on-time, high-quality delivery.

You will write key study documents, lead client meetings, and proactively manage risks. A strong background in clinical study quality, GCP, and QMS is essential; this hybrid role allows work from Cambridge or London offices.

Qualifications

• Minimum 4 years of clinical research experience.
• Experience as a project manager or study manager in clinical research is essential.
• Exposure to imaging in clinical trials is desirable.
• Strong stakeholder relationship skills.
• Excellent knowledge of ICH GCP; recent training preferred.

Responsibilities

• Take overall responsibility for operational delivery of assigned projects from initiation to close out.
• Serve as the primary point of contact for customers and internal teams.
• Write key study documents and lead client meetings; manage risks and issues.
• Report project financials and milestones for invoicing and reconciliation.
• Maintain study plans, timelines, trackers, and management documentation.
• Collaborate with site managers and data managers to deliver milestones.
• Lead meetings, prepare agendas, and document actions.
• Oversee study risks, issues, dependencies, and contingency plans.
• Deliver start-up activities and key study documents; manage change and financial performance.
• Mentor junior team members and contribute to SOPs.

Skills

Project management

Clinical research

Stakeholder management

GCP knowledge

QMS ISO standards

Education

Biomedical science degree beneficial

Job description

Qureight is seeking a Senior Clinical Study Manager to join our Clinical Operations team. You will lead start-up and ongoing study management activities, acting as the primary contact for customers and internal teams while ensuring on-time, high-quality delivery.

You will write key study documents, lead client meetings, and proactively manage risks. A strong background in clinical study quality, GCP, and QMS is essential; this hybrid role allows work from Cambridge or London offices.