Clinical Study Lead - Cardiovascular Outcomes (CVO)
Clinical Study Lead - Cardiovascular Outcomes (CVO)
The location of the role is London.
The duration of the contract is 6 months.
The pay rate on offer is £650 - £700 per day (via Umbrella agency).
Key accountabilities of the role
- Accountable to ensure all relevant studies follow company SOPs and GCP.
- With direction, may matrix with key Study conduct partners.
- Assist with maintaining relationships and monitor performance of CRO's and other vendors.
- With direction from Senior Clinical Staff, collaborate with Clinical Operations functional groups (Regional Monitoring, Data Management, and Operations Management) to ensure on time delivery of studies.
- Provide input into identifying implications of study progress upon overall timeline goals conduct plans.
- With oversight manage study start-up, conduct and close-out.
- manage clinical trial material.
- Assist in the management of CRO's or other outsourcing partners as appropriate.
- Provide input into content and execution of investigator meetings / may present selected topics.
- Provide input into development of CRF.
- Provide input into site selection with coordinated input.
Key skills and experience
- Experience in study delivery role (study leader or study manager) on cardiovascular outcomes study/ies (CVO)
- Managing complex global study footprints
- Oversight of high site volumes (100-1,000+ sites)
- Leading cross-functional study teams
- Experience with Clinical Endpoint Committees (CEC)
- Leading large, geographically dispersed teams
- Scientific understanding (cardiovascular endpoints & populations)
- Operational expertise (large, global, long-term trials)
- Analytical skills (event-driven monitoring, data interpretation)
- Leadership & communication (alignment across complex stakeholder networks)
- Familiarity with: Data Monitoring Committees (DMC/DSMB)