This role sits within ViiV Legal and will support ViiV's R&D and Global Medical organizations as they advance ViiV's portfolio, collaborations and evidence-generation activities in a highly regulated global environment.

As the Counsel, R&D and Global Medical, you will provide practical legal support to ViiV's R&D and Global Medical organizations, partnering with legal colleagues and cross-functional teams to support clinical development, medical affairs, evidence generation, research collaborations and portfolio activities across ViiV's HIV-focused pipeline and marketed medicines. You will advise on legal, privacy, contracting, governance and risk-management issues arising across the medicine lifecycle, with a focus on helping teams make well-informed decisions in a fast-moving global environment. The role requires sound judgment, clear communication, collaboration and the ability to translate legal advice into actionable guidance for scientific, medical and development colleagues.

This role will be based out of Durham, NC & may be considered for a domestic relocation package. Check out this link to learn more about the thriving, diverse, and cutting edge RTP area!

Research Triangle Park | Where People + Ideas Converge (rtp.org)

This role will provide the opportunity to support key activities across ViiV's R&D and Global Medical organizations. Responsibilities include:

• Work closely with business colleagues supporting R&D, Global Medical, clinical development, privacy, intellectual property, compliance and contracting to deliver integrated legal support across ViiV's portfolio and external collaborations.
• Draft, negotiate and review a range of R&D and Global Medical agreements, including clinical study, investigator-sponsored research, academic collaboration, consortium, data-sharing, sample-use, advisory, service and external engagement arrangements, working with internal clients and contracting teams to ensure appropriate risk allocation and operational clarity.
• Coordinate with specialist Legal and Compliance colleagues, including Global Intellectual Property, Digital Privacy and Cybersecurity, Regulatory, Compliance and the Legal Contracting Network, to support timely, practical and aligned legal advice for ViiV's R&D, medical and external scientific activities.
• Identify, assess and communicate legal and business risks arising from clinical development, medical affairs, evidence generation, data use, collaborations and external scientific engagement, and advise on practical mitigation, governance and escalation options.
• Work with Quality, Risk Management, Privacy, Compliance and Regulatory colleagues to advise on governance and risk issues relating to clinical studies, real-world evidence, medical activities, data use, human biological samples and scientific collaborations.
• Support the review and interpretation of pending or new legislation, regulations, guidance or policy developments impacting ViiV's R&D and Global Medical activities, working with Legal, Compliance, Regulatory and Policy colleagues to help assess business impact and appropriate responses.
• As needed, support legal work relating to clinical development, registration, post-approval evidence generation and lifecycle activities for one or more ViiV medicines or pipeline assets, working with senior legal colleagues and subject-matter experts as appropriate.

In accordance with GSK Performance with Choice principles, presence in the office 2-3 days each week is required.

Why you?

Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals

• Qualified lawyer authorized to practice in the US
• 3 plus years of relevant private practice and/or in-house legal experience, including life sciences, pharmaceutical, healthcare, corporate, transactional, litigation, regulatory or other experience involving complex legal analysis, risk assessment, contracting, governance or client counseling.
• Experience advising on contracting, privacy, data governance, clinical studies, medical affairs, research collaborations, human biological samples, publications or external scientific engagements.
• Working knowledge of intellectual property issues relevant to research collaborations, clinical studies, data, samples, publications and external scientific engagements, with ability to partner effectively with specialist IP counsel.
• Strong written and verbal communication skills in English, with ability to explain legal issues clearly to non-lawyers
• Ability to provide clear, practical legal advice under tight timelines and changing priorities, with appropriate escalation of complex or higher-risk issues.
• Ability to work collaboratively in a matrixed environment, build trusted relationships with legal and business colleagues, and escalate appropriately when legal or business risks require senior input.

Preferred Qualification
If you have the following characteristics, it would be a plus

• Experience working with cross-functional R&D, clinical development, medical affairs, regulatory, compliance or commercial teams in a life sciences or healthcare setting.
• Familiarity with digital health, artificial intelligence, real-world evidence, data analytics or other technology-enabled activities in a regulated life sciences environment.
• Experience coordinating with subject-matter experts and cross-functional stakeholders to support timely, practical legal advice.

#LI-ViiV

#LI-GSK

Skills
Business Acumen, Critical Thinking, Data Privacy, Legal Document Review, Legal Strategies, Negotiation, Risk Mitigation Strategies, Stakeholder Management

Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program ViiV offers US employees. All ViiV employees receive the same benefits options and plans as GSK employee.