Global Clinical Study Lead
Type: Temporary
Duration: 7 months approx. (until end of 2026)
Location: Remote (client based in London)
Rate: circa. £600-680 per day (via Umbrella, INSIDE IR35)
We are seeking 2 experienced Study Leads 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 & 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
- Experience with Oncology, Respiratory and/or Cardiovascular clinical trials
- 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
NOTE:
These roles are remote however, if you would be interested in working with the client longer-term, they encourage workers to be onsite 3 days per week (offices in Central London)
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