Global Clinical Study Manager
Type: Temporary
Duration: 7 months approx. (until end of 2026)
Location: Remote (client based in London)
Rate: circa. £500-615 per day (via Umbrella, INSIDE IR35)
We are seeking multiple experienced Study Managers 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 solid Study Management experience who can confidently take ownership of study delivery and drive successful outcomes.
Key Responsibilities
*Manage 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 Manager (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)
Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.