Clinical Study Lead
Posted 7 days ago by SRG
£680 Per day
Inside
Undetermined
London Area, United Kingdom
Summary: The Global Clinical Study Lead will be responsible for overseeing complex global clinical trials, particularly in cardiovascular outcomes studies. This role requires strong leadership and management skills to ensure successful study delivery while collaborating with cross-functional teams and external vendors. The position is initially a 7-month contract with the potential for permanent placement.
Key Responsibilities:
- Lead and oversee global clinical studies in line with SOPs and GCP requirements
- Manage study start-up, conduct, and close-out activities
- Collaborate with cross-functional teams including Clinical Operations, Data Management, and Regional Monitoring
- Oversee CROs and external vendors to ensure successful study delivery
- Support investigator meetings, site selection, and CRF development
- Monitor study timelines, risks, and operational performance
- Manage clinical trial materials and study execution activities
Key Skills:
- Global study leadership
- Cross-functional collaboration
- Vendor and CRO oversight
- Strong communication and stakeholder engagement
- Ability to manage competing priorities and tight timelines
Salary (Rate): £680 daily
City: London Area
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: inside IR35
Seniority Level: undetermined
Industry: Other
Job Title: Global Clinical Study Lead
Contract: 7 Months Initially – Temp to Perm
Rate: £680 per day (Umbrella)
Overview: We are looking for an experienced Global Clinical Study Lead to support the delivery of complex global clinical trials. This role is ideal for someone with strong study leadership experience, particularly within cardiovascular outcomes studies, and a proven ability to manage large-scale, global clinical programmes.
Key Responsibilities:
- Lead and oversee global clinical studies in line with SOPs and GCP requirements
- Manage study start-up, conduct, and close-out activities
- Collaborate with cross-functional teams including Clinical Operations, Data Management, and Regional Monitoring
- Oversee CROs and external vendors to ensure successful study delivery
- Support investigator meetings, site selection, and CRF development
- Monitor study timelines, risks, and operational performance
- Manage clinical trial materials and study execution activities
Requirements:
- Strong experience in a Study Lead or Study Manager role
- Clinical trials experience is essential
- Cardiovascular outcomes study (CVO) experience highly desirable
- Experience managing large, complex global studies with 100–1,000+ sites
- Strong leadership experience across geographically dispersed teams
- Experience with Clinical Endpoint Committees (CEC) and DMC/DSMB processes
- Excellent analytical, operational, and stakeholder management skills
- Previous experience working within large global pharma environments is advantageous
Key Skills:
- Global study leadership
- Cross-functional collaboration
- Vendor and CRO oversight
- Strong communication and stakeholder engagement
- Ability to manage competing priorities and tight timelines
This is an excellent opportunity to join a high-performing clinical operations environment and contribute to large-scale global cardiovascular studies.