Clinical Trial Manager- Part-time
Company: Cpl Agency
- Location: London, United Kingdom
- Work mode: Hybrid
- Seniority: Senior
- Employment type: Part-time
- Posted: 7 days ago
- Offer language: English
Job description
Clinical Trial Manager- Part-Time
5 month contract
Part-time
Hours: 3 days per week
Location: London (Hybrid)
We are seeking an experienced Clinical Trial Manager for a leading London Academic Research Centre to join a collaborative clinical research team responsible for the delivery of high-quality clinical studies.
This position will play a key role in the set-up, management, and oversight of clinical trials, ensuring studies are delivered on time, within budget, and in compliance with regulatory requirements, Good Clinical Practice (GCP), and study protocols. Working closely with investigators, study sites, and cross-functional stakeholders, you will drive operational excellence throughout the trial lifecycle, from start-up through to study close-out.
Key Responsibilities
- Lead the day-to-day management and coordination of clinical trials from study initiation through to completion.
- Act as the primary point of contact for investigators, participating study sites, and internal stakeholders.
- Coordinate regulatory, ethics, and site approval submissions to ensure timely study start-up.
- Develop, maintain, and oversee essential trial documentation in line with GCP and organisational procedures.
- Monitor study timelines, recruitment targets, milestones, and budgets, implementing corrective actions where required.
- Build and maintain strong relationships with study sites, providing ongoing support to drive engagement and performance.
- Coordinate site initiation, training, monitoring, and close-out activities.
- Oversee study data quality, ensuring timely data collection, query resolution, and database requirements are met.
- Monitor protocol compliance and support risk management activities, including trial risk assessments and mitigation planning.
- Manage safety reporting processes and submit required documentation to regulatory and ethics bodies.
- Prepare and present study progress updates for project teams, steering committees, sponsors, and external stakeholders.
Requirements
- Previous experience managing or coordinating clinical trials within a sponsor, CRO, academic, NHS, or research environment.
- Strong knowledge of ICH-GCP, clinical trial regulations, and research governance requirements.
- Experience with study start-up, site management, regulatory submissions, and trial oversight.
- Excellent organisational, communication, stakeholder management, and project management skills.
- Ability to manage multiple priorities in a fast-paced clinical research environment.
