Clinical Trials Manager
| Dyddiad hysbysebu: | 11 Chwefror 2026 |
|---|---|
| Oriau: | Llawn Amser |
| Dyddiad cau: | 04 Mawrth 2026 |
| Lleoliad: | City of London, London, W1T 4TJ |
| Gweithio o bell: | Hybrid - gweithio o bell hyd at 2 ddiwrnod yr wythnos |
| Cwmni: | SRG |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | BBBH174399_1770827615 |
Crynodeb
Job Description: Clinical Trials Operations Manager
Salary: £35.88 - £40.06 p/h
Hours: 36.5 hours per week / Hybrid 3 days onsite
Location: London, W1T
Contract: 12 months
Role Overview
SRG are looking for a Clinical Trials Manager for a leading higher education institute, working within the Cancer Trials Centre. The Clinical Trials Operations Manager (Regulatory) provides senior-level operational oversight across regulatory affairs, quality assurance, monitoring, and pharmacovigilance activities within a major academic cancer trials centre.
Key Responsibilities
- Clinical Trials Operations
- Strategic and operational support to senior leadership.
- Oversee quality assurance, monitoring, pharmacovigilance, and data science teams.
- Ensure adherence to protocols, GCP, SOPs, and regulations.
- Develop and refine operational systems and SOPs.
- Lead staff management, evaluations, training, and recruitment.
- Centre-Wide Responsibilities
- Contribute to Senior Management Group.
- Support funding reports and reviews.
- Liaise with MHRA and HRA.
- Lead preparation for regulatory inspections.
- Represent the centre nationally and internationally.
- General Responsibilities
- Promote organisational values and sustainability.
- Perform duties within scope of the role.
- Hybrid working option available.
Person Specification
Essential Criteria
- Degree or equivalent experience.
- Substantial experience within a trial sponsor environment.
- Knowledge of UK/EU trial regulations and pharmacovigilance.
- Understanding of clinical data management and QA.
- Experience with IMP clinical trials.
- Leadership and line management experience.
- Experience producing trial documentation.
Desirable Criteria
- Knowledge of international trial regulations.
- Experience with biological sample processing.
Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.