Senior Clinical Trial Associate

PE Global is currently recruiting for a Senior Clinical Trials Management Associate for a leading multi-national BioPharma client based in Stockley park, Uxbridge (to be moved to central London in 2027)

This is an initial 12 months contract.

Location: Stockley Park (Hybrid role 3 days onsite required, 2 days remote). Please note the offices will be moving to a central London location as of Q2 2027.

The daily rate for the role is £290.54 PAYE or £385.84 Umbrella.

Duties of the role/Responsibilities

• The Senior Clinical Trials Management Associate supports global oncology and cell therapy studies by coordinating start up activities, overseeing CRO and vendor deliverables, performing accompanied monitoring visits, and ensuring documentation and site activities comply with GCP and SOPs.
• The role works closely with cross functional partners, assists with key study materials and reporting, helps organize investigator meetings, and contributes to efficient study execution, requiring strong communication, organisation and prior clinical research experience.
• Assist global and regional trial managers with set-up of central labs and study vendors as required, including liaising with study management CRO to ensure site training and timely initiation.
• Performs accompanied visits (PSSVs, SIVs, RMVs) with CRO CRAs to ensure correct study procedures according to SOPs and protocol procedures, and review of routine regulatory documents/files in compliance with protocol, regulatory requirements, SOPs, and Monitoring Plan, as required.
• Under supervision may assist in review of protocols, informed consents, and case report forms, monitoring plans, abstracts, presentations, manuscripts and clinical study reports.
• May assist in compilation of investigator brochures under close supervision Review of trip reports generated by CRO CRAs.
• Communicates and collaborates with other functional groups.
• Assists in the Management of the CRO’s and vendor’s as required.
• Assists with the preparation and organization of international investigator meetings
• Assists in preparation of safety, interim and final study reports, including resolving data discrepancies. Performs administrative duties in a timely manner as assigned.
• Travel may be required 1 or 2 times per year (a few days)

Education/Experience

• Educated to degree level or equivalent in a scientific discipline.
• Previous experience of pharmaceutical clinical trial experience.
• CRA experience is highly desired.
• Oncology experience is required / CAR-T Cell Therapy would be desirable.
• Excellent verbal, written, interpersonal and presentation skills are required.
• Must be familiar with routine medical/scientific terminology.
• Must be proficient with Word, PowerPoint, and Excel.
• Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable.

Interested candidates should submit an updated CV.

Please click the link below to apply.

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***