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

1. 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.

2. 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.

3. 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.