Clinical Sciences Manager, Global Collaborative Studies - ViiV Healthcare 10 month maternity cover

Site Name: UK - London - New Oxford Street, Durham Blackwell Street Posted Date: May 21 2026 This fixed-term role represents a great opportunity to work in the ViiV Healthcare Global Collaborative Studies Group, which currently supports over 120 investigator sponsored research (ISR) studies, generating important evidence to inform use of our products, and HIV in general, across the world. In this role, you will lead, manage and implement the company related activities and accountabilities for ViiV Healthcare supported studies including investigator sponsored studies (ISS) and supported collaborative studies (SCS), ensuring timely review of study proposals and start up activities and compliance with relevant SOPs and policies from study start to completion. 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 will include (but not limited to): 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 Safety of study subjects through sound study design and analysis, and appropriate safety data exchange for the study Regulatory compliance including compliance with clinical trial agreement (CTA), maintenance of audit-worthy study files/documentation, and availability & visibility of study documentation and progress Scientific and ethical merit and quality of study design, execution, analysis, interpretation and disclosure of data Accurate tracking of study milestones and financial milestones Accurate tracking of drug supply and timely escalation to the Drug Supply Team 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 have current knowledge of HIV therapy area Leadership experience in a matrix environment Equal Opportunity Employer Statement 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. #J-18808-Ljbffr National Society for Black Engineers