Clinical Study Lead – Cardiovascular Outcomes (CVO)
Location: London
Duration: 6 months
Pay rate: £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 CROs 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 CROs 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).
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