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)
JBRP1_UKTJ