Key Responsibilities
* Serve as the ViiV point of contact (Study Accountable Person (SAP)) for multiple ISS and SCS, managing company related accountabilities and activities for review, start‑up, contracting, milestone management, budget and/or drug supply, and data disclosure from submission to completion, ensuring optimal communication between external and internal stakeholders.
* Lead scientific, strategic and ethical review of ISS and SCS proposals from external collaborators/sponsors.
* Act as the main contact for Global Medical Leads (GMLs), Medicine Development Leads, and other functional partners on individual supported studies.
* Partner with GMLs and external sponsors to develop supported collaborative study proposals, protocols, and support implementation in line with ViiV strategy.
* Build and maintain strong, productive relationships with external organisations and investigators across global institutions.
* Work cross‑functionally with internal stakeholders to ensure compliant, efficient end‑to‑end delivery and communication of ViiV support for ISS and SCS. Key collaborating functions include Safety, Legal, Clinical Operations, Clinical Supply, Regulatory, Statistics, Finance, Scientific Communications and Medical Affairs.
* Contribute to strategy and integrated evidence teams, including providing ISS and SCS insights for product specific Global Integrated Evidence Plans.
Accountability
* Ensure compliance with relevant SOPs and policies from study start to completion with support from relevant stakeholders, in particular
o Safety of study subjects through sound study design and analysis, and appropriate safety data exchange for the study.
o Regulatory compliance including compliance with clinical trial agreement (CTA), maintenance of audit‑worthy study files/documentation, and availability & visibility of study documentation and progress.
o Scientific and ethical merit and quality of study design, execution, analysis, interpretation and disclosure of data.
o Accurate tracking of study milestones and financial milestones.
o Accurate tracking of drug supply and timely escalation to the Drug Supply Team.
o Issue management of results from studies.
Basic Qualifications
* Life Science degree (PharmD, PhD, MD, etc).
* Experience in pharmaceutical industry supported study/clinical research.
* Understand clinical trials from study concept to publication.
* Strong communication and negotiation capabilities.
* Strong teamworking and relationship building skills with external and internal partners across multiple functional areas.
Preferred Qualifications
* Experience in Medical Affairs and current knowledge of HIV therapy area.
* Leadership experience in a matrix environment.
Closing Date for Applications: Thursday, 4th June 2026.
ViiV is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
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