Clinical Study Manager
Location: Flexible / Hybrid
Sector: Clinical Research
Salary: Competitive + Benefits
CY Partners are currently recruiting for an experienced Clinical Study Manager to join a leading organisation delivering large-scale global cardiovascular outcomes studies. This is an excellent opportunity for a clinical operations professional with strong leadership capability and extensive experience managing complex international trials.
The Role
As Clinical Study Manager, you will be responsible for leading the delivery of global cardiovascular outcomes (CVO) studies, ensuring operational excellence across all phases of study execution. You will work collaboratively with cross-functional teams, external vendors, and key stakeholders to drive study performance, quality, and timelines.
Key Responsibilities
- Lead and oversee complex global cardiovascular outcomes studies
- Manage studies involving high-volume site networks (100–1,000+ sites)
- Coordinate and lead cross-functional study teams across multiple regions
- Provide oversight and collaboration with Clinical Endpoint Committees (CEC)
- Lead large, geographically dispersed operational teams
- Monitor study progress using event-driven metrics and data interpretation
- Ensure effective stakeholder communication and alignment throughout study delivery
- Support governance activities involving Data Monitoring Committees (DMC/DSMB)
- Drive operational excellence across large, global, long-term clinical trials
Requirements
We are looking for candidates with:
- Proven experience in a study delivery role such as Study Leader or Clinical Study Manager
- Strong background in cardiovascular outcomes (CVO) studies
- Excellent scientific understanding of cardiovascular endpoints and patient populations
- Demonstrated operational expertise within complex global clinical trials
- Strong analytical and problem-solving skills
- Experience managing and influencing cross-functional stakeholders
- Excellent communication and leadership capabilities
- Familiarity with Clinical Endpoint Committees (CEC) and Data Monitoring Committees (DMC/DSMB)
Desirable
- Experience working within large pharmaceutical, biotech, or CRO environments
- Previous involvement in long-duration, event-driven studies
- Global trial management experience across multiple regulatory regions
Why Apply?
- Opportunity to work on high-profile global cardiovascular programmes
- Collaborative and innovative working environment
- Strong career development and progression opportunities
- Competitive salary and comprehensive benefits package
To find out more or apply, please contact the clinical team at CY Partners Careers.