We are hiring a highly experienced and proactive Clinical Trial Manager (CTM) to lead and manage full-cycle clinical trial operations. In this role, you will oversee the planning, initiation, execution, and closeout of Phase I–IV trials across therapeutic areas, ensuring compliance with ICH-GCP, MHRA, and sponsor guidelines.
You’ll serve as a strategic point of contact for internal teams, CROs, clinical sites, and vendors — delivering high-quality clinical trials on time and within budget. This is an excellent opportunity for a professional looking to advance their leadership career in clinical research management.
* Oversee clinical trial planning and implementation from protocol development through final study report
* Lead cross-functional teams (CRA, Data Management, Regulatory, Biostatistics) and manage CRO oversight
* Develop and manage study budgets, timelines, and site selection
* Monitor trial metrics, risk mitigation plans, and vendor performance
* Ensure quality and regulatory compliance with ICH-GCP, EMA, MHRA, and FDA standards
* Serve as main point of contact for clinical sites, investigators, and stakeholders
* Coordinate and lead internal/external team meetings and status reports.
* Manage documentation and trial master files (TMF) to inspection-ready standards
Requirements
Required Skills
* Extensive understanding of clinical trial regulations, GCP, ICH, and MHRA requirements
* Proven experience managing global or multi-site clinical studies
* Excellent leadership, team coordination, and stakeholder management skills
* Strong command of trial budget and vendor oversight
* Proficient with EDC systems, CTMS, and MS Office tools
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Desired Skills
* Life sciences or health sciences degree (BSc, MSc, or equivalent)
* ACRP, SOCRA, or equivalent clinical research certification
* Experience with oncology, rare disease, or CNS trials
* Familiarity with EU CTR and decentralised trial models
Benefits
Job Benefits
* Competitive salary with performance-based bonus
* Private medical insurance & pension scheme
* Career development pathway with leadership training
* Flexible hybrid working (2–3 days office-based)
* Opportunity to manage global, multi-centre trials