Clinical Study Lead - Cardiovascular Outcomes (CVO)

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)