Global Clinical Study Manager Type: Temporary Duration: 7 months approx. (until end of 2026) Location: Remote (client based in London) Rate: circa. £(Apply online only) 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 deliverySkills & 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