Senior Clinical Study Lead — Start-Up & Delivery Expert

Qureight Ltd; Greater London; Hybrid; GBP 75,000 - 110,000; Full time

Benefits offered by this job

Annual bonus

Private medical insurance

Life insurance

Cycle-to-work scheme

Contributory pension

Equity

Job summary

Qureight Ltd is seeking a Senior Clinical Study Manager to lead study start-up and ongoing management. You’ll be the primary contact for customers and internal teams, writing key documents, leading meetings, and proactively managing risks. Hybrid role based in Cambridge or London.

You will report on milestones, manage budgets, and ensure delivery to high quality standards in line with GCP, ISO and privacy regulations. Strong stakeholder and leadership skills are essential.

Qualifications

• Minimum 4 years of clinical research experience, ideally in imaging CR Organisation or similar.
• Experience as a project/study manager in clinical research essential, with focus on lung/heart trials desirable.
• Experience with clinical trial imaging is highly desirable but not essential.
• Demonstrated ability to cultivate key stakeholder relationships.
• Excellent knowledge of ICH GCP with recent training.
• Experience in a Quality Management System (e.g., ISO 9001, ISO 13485).
• Familiarity with regulatory standards (e.g., 21 CFR Part 11).
• Strong written and verbal communication skills.
• Proven problem-solving in a technical, innovative environment.
• Project management qualification or experience.

Responsibilities

• Take overall responsibility for operational delivery of assigned studies from initiation to close out.
• Act as SME for assigned studies, oversee study-specific requirements and performance.
• Develop and maintain study plans, timelines, trackers and docs.
• Support site managers and data managers in achieving milestones.
• Lead client meetings and maintain strong client relationships.
• Own change control, assess impact on scope, timelines and finances.
• Oversee study financial milestones, forecasting, invoicing and tracking.
• Ensure compliance with Qureight SOPs, GCP, ISO standards and data privacy.

Skills

Project management

Clinical research

Stakeholder management

Regulatory knowledge

Education

Biomedical science degree (beneficial)

Job description

Qureight Ltd is seeking a Senior Clinical Study Manager to lead study start-up and ongoing management. You’ll be the primary contact for customers and internal teams, writing key documents, leading meetings, and proactively managing risks. Hybrid role based in Cambridge or London.

You will report on milestones, manage budgets, and ensure delivery to high quality standards in line with GCP, ISO and privacy regulations. Strong stakeholder and leadership skills are essential.