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

United Kingdom; United States, London Employment contract · Job Posted May 27, 2026

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Job Description

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.

Job Responsibility

  • 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
  • Contribute to strategy and integrated evidence teams, including providing ISS and SCS insights for product specific Global Integrated Evidence Plans
  • Ensure compliance with relevant SOPs and policies from study start to completion with support from relevant stakeholders

Requirements

  • 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

Nice to have

  • Experience in Medical Affairs and have current knowledge of HIV therapy area
  • Leadership experience in a matrix environment

What we offer

  • Competitive base salary
  • Annual bonus based on company performance
  • Flexible working options available for most roles
  • Learning and career development
  • Access to healthcare & wellbeing programmes
  • Employee recognition programmes
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