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Clinical Director

Job in Greater London, London, Greater London, W1B, England, UK
Listing for: Cpl Group
Full Time position
Listed on 2026-10-07
Job specializations:
  • Healthcare
    Healthcare Management
Salary/Wage Range or Industry Benchmark: 90000 - 120000 GBP Yearly GBP 90000.00 120000.00 YEAR
Job Description & How to Apply Below
Clinical Operations Lead – Gene Therapy

An exciting opportunity for an experienced Clinical Operations leader to join a fast-moving, entrepreneurial biotech developing innovative gene therapy programmes in neurological and psychiatric diseases. This highly empowered, hands-on position will lead late-stage clinical delivery, combining operational rigour with a forward-looking approach to technology, evidence generation and commercial readiness.

Key responsibilities:
  • Lead the operational planning, set-up and execution of Phase II/III and pivotal clinical trials, including country, site and vendor selection.
  • Establish and support QMS development, protocols and regulatory submissions.
  • Oversee CROs, vendors and study teams, ensuring quality, timelines, budgets and operational risks are effectively managed.
  • Drive investigator and site engagement, patient recruitment, data quality, safety surveillance and inspection readiness.
  • Identify and implement pragmatic AI and digital solutions to improve trial execution, enrolment and safety monitoring.
  • Support evidence generation for registration, reimbursement, payer discussions and future commercial launch.
  • Build clear internal reporting and dashboards to provide visibility of programme progress, risks and priorities.
Experience required:
  • 10+ years’ experience in clinical operations, clinical development operations or clinical programme leadership within biotech, pharma or CRO environments.
  • Demonstrated leadership of Phase II/III or pivotal multi-country/global trials.
  • Strong experience managing CROs, vendors, budgets, timelines, quality and risk.
  • Sound knowledge of ICH-GCP, clinical trial regulations, patient safety and data integrity.
  • Experience establishing a QMS and supporting clinical protocol design.
  • A hands-on, entrepreneurial mindset and confidence working in a lean, rapidly evolving environment.

Gene therapy, CNS/neuropsychiatry, registration-enabling Phase III programmes and AI/digital clinical-trial technology experience would be highly advantageous.

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