Clinical Study Lead - Imaging Trials (Hybrid)

Qureight Ltd; Greater London; Hybrid; GBP 65,000 - 82,000; Full time

Benefits offered by this job

Annual bonus

Private medical insurance

Life insurance

Cycle-to-work scheme

Contributory pension

Equity

Additional leave

Job summary

Qureight Ltd is seeking an experienced clinical study manager to join our Clinical Operations team. Based in Cambridge or London, you will lead start-up and ongoing management of allocated studies, ensuring milestones are met and deliverables are of high standard.

You will work with cross-functional colleagues, monitor progress, manage budgets and invoicing, and ensure compliance with GCP, ISO27001, data privacy, and related regulations.

Qualifications

• Minimum of 2 years of clinical research experience, ideally in an imaging CRO or other clinical trial delivery environment.
• Experience as a project manager or startup specialist in clinical research is desirable, with a focus on lung and heart trials.
• Experience with clinical trial imaging is highly desirable but not essential.
• Demonstrated ability to cultivate and maintain key stakeholder relationships, both internally and externally.
• Knowledge of ICH GCP with evidence of recent training.
• Experience working within a Quality Management System (QMS), e.g., ISO 9001, ISO 13485.
• Knowledge of relevant regulatory, compliance and industry standards, e.g. 21 CFR Part 11.
• Strong interpersonal and communication skills.

Responsibilities

• Lead the delivery of assigned customer projects/clinical studies from kick-off through maintenance and close-out.
• Develop and maintain study plans, timelines, trackers and other study management documentation.
• Monitor study progress against milestones, identifying risks and dependencies early.
• Coordinate and lead study meetings, prepare agendas and status updates, ensure actions are followed up.
• Collaborate with customers to understand project goals and establish requirements.
• Work with internal and external stakeholders at agreed frequencies to ensure alignment.
• Support clinical site managers and data managers in delivering milestones.
• Deliver start-up activities, including Kick-off Meetings and key study documents.

Skills

Clinical research

Project management

Stakeholder management

Regulatory awareness

Education

Biomedical science degree (beneficial)

Tools

GCP knowledge

QMS ISO standards

Job description

Qureight Ltd is seeking an experienced clinical study manager to join our Clinical Operations team. Based in Cambridge or London, you will lead start-up and ongoing management of allocated studies, ensuring milestones are met and deliverables are of high standard.

You will work with cross-functional colleagues, monitor progress, manage budgets and invoicing, and ensure compliance with GCP, ISO27001, data privacy, and related regulations.