GSK Vaccines
Healthcare
ProjectPhysician
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Project Physician at GSK Vaccines. Skills: Clinical development, Drug safety, Vaccines. Lead clinical development of vaccine programmes. Design clinical trials”
What You'll Achieve.
Demonstrate Proof of Concept; Ensure high quality clinical data delivery; Ensure on-time clinical data delivery; Achieve high standards; Attain project timelines
Industry & Context.
Finding solutions to challenges; Independent issue resolution; Independent decision-making
What They're Looking For.
Must Have
Doctor of Medicine with advanced university degree, Board certification, 2-3 year experience in industry clinical development, 10 years working in scientific or medical Institution, Medical and scientific knowledge in infectious diseases, Experience in clinical development and drug safety in academia or industry, Experience finding solutions in clinical development in LMICs
Nice to Have
Innovative problem solving, Clinical leadership, Excellent interpersonal skills, Excellent communication skills, Interact with tact, respect and cultural sensitivity, High level of impact and accountability, Independent issue resolution, Independent decision-making, Generate, interpret and communicate complex clinical data, End-to-end responsibility for results, Scientific dissemination with limited supervision
What You'll Do.
Lead clinical development of vaccine programmes
Design clinical trials
Set-up clinical trials
Serve as lead author of clinical documents
Serve as key contributor of clinical documents
Have medical monitoring responsibility for clinical trials
Ensure high quality clinical data delivery
Ensure on-time clinical data delivery
Demonstrate Proof of Concept
Adhere to good clinical practices
Adhere to GSK Vaccines SOPs
Be a member of the Safety Review Team
Author clinical development plans
Write Investigator Brochures
Write clinical study reports
Address scientific issues related to trials
Address medical issues related to trials
Provide oversight of medical monitoring team
Review Medical Data Listing
Ensure medical consistency within trial
Ensure medical consistency across trials
Provide oversight for medical assessment
Assess serious adverse events
Assess adverse events of special interest
Assess other events during clinical trials
Pay attention to potential safety signals
Participate in safety report compliance
Take corrective actions
Handle studies with human biological samples
Coordinate studies with human biological samples
Support Senior project physician Lead
Represent GVGH in meetings with health authorities
Represent GVGH in meetings with scientific community
Network with thought leaders
Network with international agencies
Contribute to creation of standards
Contribute to review of standards
Contribute to revision of standards
Maintain knowledge in vaccines
Maintain knowledge in clinical trial methodology
Maintain knowledge in drug safety competencies
Maintain knowledge in national regulations
Maintain knowledge in international regulations
Maintain knowledge in Global Safety policies
Serve as principal liaison to Safety Committee
Serve as principal liaison to Data Management Committee
Author program strategy
Author clinical development plans for governance
Author clinical trial design for governance
Ensure consistency of data within program
Ensure consistency of data across projects
Support clinical team to achieve high standards
Support clinical team to achieve project timelines
Ensure milestone realization
Ensure resource optimization
How You'll Work.
Team & Collaboration
Cross functional Safety Review Team; Clinical Development sub-team; GVGH Project Team; Matrix team
Communication Scope
Clinical documents; Publications; Scientific dissemination; Health authority meetings; Scientific community meetings
Process & Methodology
Clinical development plans, Clinical trial protocols, Program strategy
Full Job Description
**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
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