Job Details

Global Clinical Study Lead

Type: Temporary
Duration: 12 months (tbc)
Location: Remote (client based in London)
Rate: circa. -(Apply online only) per day (via Umbrella, INSIDE IR35)

We are seeking an experienced Study Lead to oversee the delivery of complex studies from initiation through to completion. This is a key role requiring strong leadership, operational oversight, and the ability to drive high-quality study execution in a fast-paced environment.

This role is ideal for candidates with established Study Lead experience who can confidently take ownership of study delivery and drive successful outcomes.

Key Responsibilities

• Lead end-to-end study delivery, ensuring milestones, timelines, and budgets are met
• Act as the primary point of accountability for study execution and performance
• Coordinate cross-functional teams (clinical, data, regulatory, vendors) to ensure alignment
• Oversee study planning, risk management, and issue resolution
• Ensure compliance with regulatory requirements, SOPs, and quality standards
• Manage vendor relationships and external partners to ensure effective delivery

Skills andamp; Experience Required

• Proven experience as a Study Lead (essential) with ownership of full study life-cycle
• Strong understanding of clinical/trial or research study processes and governance
• Demonstrated ability to manage multiple stakeholders and cross-functional teams
• Excellent project management, planning, and organisational skills
• Strong leadership, communication, and problem-solving capabilities
• Experience working within regulated environments (e.g. GCP or equivalent) is highly desirable

Guidant, Carbon60, Lorien andamp; SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.