Director, ABPI Governance & Medical Signatory Excellence

Posted 2 hours 3 minutes ago by GlaxoSmithKline

Permanent
Full Time
Other
London, United Kingdom
Job Description
Director, ABPI Governance & Medical Signatory Excellence

We are a specialist pharmaceutical company 100% dedicated to developing medicines to treat and prevent HIV.

As the pioneers in HIV innovation, we constantly look to push the boundaries of science to develop medicines that can change lives and give people more choice. Beyond our medicines, we are proud of our deep connection with the HIV community and work with partners to advance research and development, address HIV-related stigma, increase access to our medicines and provide funding and support to local community organisations to support their efforts in the HIV response. We are ViiV Healthcare. Here until HIV and AIDS are not.

Position Summary

You will provide enterprise leadership for ABPI Code governance, medical signatory excellence, and compliant scientific communication across ViiV. Act as the organisation's senior expert on the interpretation, application, and evolution of the ABPI Code, ensuring compliant promotional and non promotional activities globally and in the UK. Strengthen medical governance frameworks, mitigate compliance risk, and uphold scientific integrity and corporate reputation.

This is an individual contributor role, requiring hands on technical expertise, personal accountability for complex ABPI Code assessments, and direct involvement in high risk, high impact scientific and promotional review and decision making, alongside providing strategic leadership and guidance to the wider organisation.

Key Responsibilities
  • Serve as the senior ABPI Code authority, providing expert interpretation, strategic direction, and governance across ViiV healthcare including the impact on markets ex-UK and cross functional teams.
  • Act as a nominated Final Medical Signatory, conducting expert review and certification of complex, high visibility, or high risk materials and activities.
  • Lead the global medical signatory community, setting standards, capabilities, and performance expectations to drive excellence and consistency in decision making.
  • Own and evolve global ABPI governance frameworks, policies, and approval pathways to ensure efficient, predictable, compliant processes.
  • Oversee escalations, including PMCPA/MHRA cases, inter company dialogue, and complex compliance issues requiring senior adjudication.
  • Provide proactive risk assessment and mitigation for launches, scientific platform development, external engagement strategies, and major content initiatives.
  • Shape scientific and claims substantiation standards, ensuring evidence based, balanced, and compliant medical and promotional communication.
  • Lead capability building programmes for signatories, reviewers, medical/scientific teams, and cross functional stakeholders.
  • Advise senior leadership, including the Chief medical officer, global medical leads, regional medical and commercial heads on ABPI topics influencing strategy and reputation.
  • Represent ViiV/GSK in external and cross industry forums, contributing to policy shaping, Code interpretation harmonisation, and future ABPI/EFPIA developments.
Basic Qualification
  • UK registered Medical Doctor (GMC) or Pharmacist (GPhC).
  • Expert level knowledge of ABPI, EFPIA, PAGB, and MHRA Blue Guide.
  • Experience as a nominated Final Medical Signatory under the ABPI Code.
  • Demonstrated leadership in ABPI governance, decision making, compliance frameworks, and/or complaint resolution.
  • Strong ability to evaluate scientific evidence, claims substantiation, and risk benefit communication.
  • High judgement in resolving ambiguous or high stakes compliance issues.
  • Strong communication skills and ability to influence senior stakeholders.
  • Experience developing training, capability frameworks, and inspection ready systems.
  • Ability to manage cross functional decision making and governance processes.
Preferred Experience
  • Experience shaping cross functional governance or enterprise systems.
  • Medical leadership in a global or regional role.
  • Experience in launch excellence, scientific platform development, and evidence review.
Location

Hybrid working applies to this role and it is based at our UK HQ, Central London. (2/3 days a week onsite).

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.