Clinical Trial Manager (CTM) - Remote Permanent Entrust Resource Solutions are supporting an innovative and rapidly growing biotechnology organisation in the search for a Clinical Trial Manager to support the operational delivery of clinical studies within a fast-paced and collaborative clinical development environment.
This is an exciting opportunity for an experienced Clinical Operations professional to play a key role in the planning, execution, oversight, and close-out of sponsor-managed clinical trials. The successful individual will work closely with internal stakeholders, CROs, clinical sites, and external vendors to ensure studies are delivered on time, within budget, and in compliance with ICH-GCP and regulatory requirements.
Key Responsibilities: - Support operational delivery of clinical studies from study start-up through to close-out
- Coordinate site feasibility, study start-up, and ongoing site management activities
- Support oversight and management of CROs, vendors, and external service providers
- Manage study documentation and clinical systems including CTMS and eTMF
- Support deviations, CAPA activities, and inspection readiness processes
- Track study timelines, budgets, purchase orders, and invoice activities
- Ensure Trial Master File quality, completeness, and audit readiness
- Support data review, query management, and study reporting activities
- Prepare meeting materials, study metrics, operational updates, and action trackers
- Contribute to process improvements and Clinical Operations best practices
Candidate Requirements: - Previous experience within Clinical Operations, Clinical Trial Management, or Clinical Project support roles
- Strong understanding of ICH-GCP and clinical trial regulations
- Experience supporting sponsor-managed or outsourced clinical studies
- Experience working with CROs, clinical sites, vendors, and cross-functional stakeholders
- Familiarity with CTMS, eTMF, and clinical trial documentation systems
- Experience supporting deviations, CAPAs, and audit or inspection readiness activities
- Strong organisational, communication, and stakeholder management skills
- Ability to manage multiple priorities within a fast-paced biotech or pharmaceutical environment
This is an excellent opportunity to join a growing and innovative organisation where you will contribute to the delivery of cutting-edge clinical development programmes within a supportive and ambitious team environment.
To find out more, call Lynsey today on 07712412095 or send an up to date CV to Lynsey@Lynsey@entrustrs.com