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)