* Accountable for attracting, planning, execution and monitoring of clinical trials through all phases (from feasibility to close-out) in conformance to ICH-GCP, relevant SOPs, other procedural documents and local regulations, ensuring inspection-readiness in UK.
* Primary point of contact for Health Authority agencies for activities related to clinical operations.
* Country legal representative for GCO related activities (authorized to sign contracts and agreements).
* Accountable for functional budget and affiliate funding in compliance with relevant financial processes