Clinical Study Manager

Role: Clinical Study Manager

Location: Welwyn Garden City, Hertfordshire (Hybrid - 3 days in office)

Hours: Full-time

Contract: 12 months, Inside IR35

Pay: £377.64 - £415.29 per day PAYE basic excluding holiday pay or £500 - £550 per day Umbrella

An excellent opportunity has arisen for an experienced Clinical Study Manager to join one of our longstanding clients, a leading global healthcare organisation based in Welwyn Garden City.

This role focuses on the delivery and management of early-phase clinical trials, working closely with international study teams, clinical sites and external vendors to ensure successful study execution.

Benefits:

25 days holiday + bank holidays

Hybrid working, 3 days per week on-site

On-site, free parking

Opportunity to work within a leading global healthcare organisation

Exposure to innovative early-phase clinical trials

Collaboration with international clinical research teams

The

Requirements

Proven experience as a Clinical Study Manager within the pharmaceutical or healthcare industry

Multi-country clinical study management experience is essential

Strong experience managing external vendors and CROs

Experience delivering early-phase clinical trials

Good understanding of ICH-GCP and clinical trial regulations

Experience managing study documentation, timelines and operational risks

Excellent communication and stakeholder management skills

Proactive, organised and confident working independently

Must be able to attend the Welwyn Garden City office 3 days per week

The Role:

Manage the operational delivery of early-phase clinical studies

Coordinate multi-country study activities and clinical trial timelines

Support protocol design, feasibility assessments and country selection

Oversee clinical site start-up and patient recruitment activities

Manage vendor relationships, performance and contractual deliverables

Maintain study documentation, including Trial Master Files and informed consent forms

Oversee clinical trial supplies and investigational medicinal product

requirements

Identify and manage study risks, issues and operational challenges

Work closely with cross-functional teams to ensure study quality and compliance

Support improvements to clinical study processes and operational efficiency

If you're keen to join an exceptional team where you can use your clinical study management expertise to support innovative clinical trials, then please apply to this Clinical Study Manager role below or call Chloe McCausland on (phone number removed) between 8:30am - 5:00pm