Clinical Study Lead

Global Clinical Study LeadType

TemporaryDuration

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 ResponsibilitiesLead end-to-end study delivery, ensuring milestones, timelines, and budgets are metAct as the primary point of accountability for study execution and performanceCoordinate cross-functional teams (clinical, data, regulatory, vendors) to ensure alignmentOversee study planning, risk management, and issue resolutionEnsure compliance with regulatory requirements, SOPs, and quality standardsManage vendor relationships and external partners to ensure effective deliverySkills & Experience RequiredProven experience as a Study Lead (essential) with ownership of full study life-cycleStrong understanding of clinical/trial or research study processes and governanceDemonstrated ability to manage multiple stakeholders and cross-functional teamsExperience with Oncology, Respiratory and/or Cardiovascular clinical trials Excellent project management, planning, and organisational skillsStrong leadership, communication, and problem-solving capabilitiesExperience 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)