Global Clinical Study Lead - Cardiovascular
CV-LibraryLondontemporaryPosted: 6 May 2026
Apply NowGlobal 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 deliverySkills & 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 & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy
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 deliverySkills & 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 & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy