ProjectPhysician

**Job title:** Project Physician **Location** : Siena, Italy **Employment type:** Permanent, full time **Closing date for applications:** 19 June 2026 **Position Summary** To Lead Clinical development of One or more GVGH Vaccine Development Programmes through the design and set-up of GVGH-managed clinical trials To serve as lead author or key contributor of clinical and epidemiology plan and clinical documents (e.g., clinical trial protocols, reports and publications, integrated clinical documents for regulatory submissions etc.) and to have medical monitoring responsibility for clinical trials of GVGH vaccine project(s). In order to ensure the high quality and on-time delivery of all clinical data that will allow demonstration of Proof-of Concept of GVGH candidate vaccines in line with the clinical development plan, good clinical practices (GCP), and GSK Vaccines/ GVGH standard operating procedures (SOP). To be a member of the cross functional Safety Review Team coordinated by SERM **Responsibilities** Work in a Clinical Development sub-team of clinical and regulatory colleagues (clinical development, clinical operations, biostatistics & regulatory associates), and in collaboration with non-CDRA members of the GVGH Project Team(s), with the responsibility to author clinical development plans, design clinical trial protocols, write Investigator Brochures, clinical study reports and publications of the project(s) to high scientific, operational and ethical standards. • Address scientific and medical issues related to trials of the project(s) in GVGH. • Be responsible (or provide oversight of delegated CRO medical monitoring team) for Medical Data Listing review, ensuring medical consistency within trial and across trials within the project. • As a member of the Safety Review Team, be accountable (through providing oversight if applicable of delegated CRO medical monitoring team) for medical assessment of serious adverse events, adverse events of special interest (AES