Hybrid Clinical Study Lead – Imaging Trials

Qureight; Cambridge; Hybrid; GBP 60,000 - 90,000; Full time

Benefits offered by this job

Annual bonus

Private medical insurance

Life insurance

Cycle-to-work scheme

Contributory pension

Equity

28 days holiday

Job summary

Qureight, with offices in Cambridge and London, seeks an experienced Clinical Study Manager to drive study start-up and ongoing management for allocated studies. You will ensure deliverables meet time, cost and quality targets, coordinating with clinical operations, data managers, and finance to report milestones and invoicing details.

This role requires strong knowledge of GCP, ISO27001-like standards, and regulatory requirements, plus a proactive, collaborative attitude to ensure successful

Qualifications

• Experience in clinical research, ideally in imaging CRO or trial delivery.
• Project management or start-up experience in clinical research is desirable, with lung/heart trials focus.
• Experience with clinical trial imaging is highly desirable but not essential.
• Demonstrated ability to manage stakeholder relationships internally and externally.
• Knowledge of GCP with recent training.
• Experience within a Quality Management System (ISO 9001/13485).
• Knowledge of regulatory standards like 21 CFR Part 11.

Responsibilities

• Lead delivery of customer projects/clinical studies from kick-off to close-out.
• Develop and maintain study plans, timelines and trackers.
• Monitor progress, risks and dependencies early.
• Coordinate study meetings and document actions.
• Define project requirements with customers and set expectations.
• Collaborate with internal/external stakeholders at planned frequencies.
• Support clinical site managers and data managers toward milestones.
• Lead start-up activities and prepare key study documents.
• Own change and risk management at the project level.
• Monitor financial milestones and assist invoicing and tracking.
• Deliver study management activities in line with GCP, ISO, and data privacy rules.
• Support process improvement in Clinical Operations.

Skills

Clinical research experience

Imaging clinical trials

Stakeholder management

GCP knowledge

QMS knowledge

Regulatory compliance

Project management

Communication skills

Problem solving

Attention to detail

Startup management

Education

Biomedical science degree

Project management qualification

Job description

Qureight, with offices in Cambridge and London, seeks an experienced Clinical Study Manager to drive study start-up and ongoing management for allocated studies. You will ensure deliverables meet time, cost and quality targets, coordinating with clinical operations, data managers, and finance to report milestones and invoicing details.

This role requires strong knowledge of GCP, ISO27001-like standards, and regulatory requirements, plus a proactive, collaborative attitude to ensure successful