Provides leadership, oversight and manages the activities of within-country operational planning and delivery of Phase I-IV clinical trials in a specific country or cluster of countries; across all oncology areas (solid and blood) to the required quality standards, GSK written standards, local regulations and ICH GCP.
Key Responsibilities
Leads the local study team consisting of within-country clinical operations team members, cross-functional experts (clinical, biostats, medical, regulatory, supply logistics, finance, legal, etc.), vendor staff and external clinical site staff involved in study preparation and delivery; providing both matrix leadership and project management of study activities within the countr(ies).
Serves as the operational point-of-contact between the central GSK study team and within-countr(ies) study team. The LDL collaborates closely with local clinical, biostats, medical and regulatory affairs staff to ...