Hybrid Clinical Study Manager: Start-Up & Delivery Lead

Qureight; Greater London; Hybrid; GBP 60,000 - 90,000; Full time

Benefits offered by this job

Annual bonus

Private medical insurance

Life insurance

Cycle-to-work

Contributory pension

29 days holiday

Job summary

Qureight is seeking an experienced Clinical Study Manager to join its Clinical Operations team in the UK. You will drive study start-up and ongoing management, ensuring deliverables meet high standards and milestones are achieved.

You will partner with operational colleagues to report finances and support invoicing, while ensuring QA and regulatory compliance throughout the study lifecycle. The role is hybrid, based out of Cambridge or London, and requires a proactive, detail-focused mindset

Qualifications

• 2+ years of clinical research experience, preferably in imaging or trial delivery environments.
• Experience as a PM or start-up specialist in clinical research desirable, with focus on lung/heart trials.
• Knowledge of ICH-GCP and regulatory standards; familiarity with QMS (ISO 9001/13485) and 21 CFR Part 11.

Responsibilities

• Lead delivery of assigned customer projects/clinical studies from kick-off to close-out.
• Develop and maintain study plans, timelines, trackers and other study management docs.
• Monitor progress against milestones, identify risks and dependencies early.
• Coordinate study meetings, prepare agendas and update statuses.
• Collaborate with customers to define project goals and requirements.
• Communicate with stakeholders across internal and external teams.
• Support clinical site managers and data managers to hit milestones.
• Lead start-up activities and prepare key study documents.
• Manage project-level change and risk; track financial milestones with Finance.

Skills

Study management

GCP knowledge

Stakeholder management

Regulatory awareness

Communication skills

Project management

Education

Degree in life sciences

Job description

Qureight is seeking an experienced Clinical Study Manager to join its Clinical Operations team in the UK. You will drive study start-up and ongoing management, ensuring deliverables meet high standards and milestones are achieved.

You will partner with operational colleagues to report finances and support invoicing, while ensuring QA and regulatory compliance throughout the study lifecycle. The role is hybrid, based out of Cambridge or London, and requires a proactive, detail-focused mindset