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Waltham, Massachusetts, United States GSK Full timeCLOSING DATE: Tuesday 28th October 2025Are you an exceptional clinical development leader in Hepatology, driven to advance cutting-edge science and deliver impactful medicines to patients? If so, this VP Clinical Development, Clinical Research Head Hepatology position offers a unique opportunity to lead and innovate within GSK's advanced portfolio.GSK seeks...
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VP Clinical Development, Clinical Research Head Hepatology
4 weeks ago
Are you an exceptional clinical development leader in Hepatology, driven to advance cutting‑edge science and deliver impactful medicines to patients? If so, this VP Clinical Development, Clinical Research Head Hepatology position offers a unique opportunity to lead and innovate within GSK’s advanced portfolio. Overview GSK seeks an outstanding leader in clinical development to join as VP Clinical Development, Clinical Research Head Hepatology within the Advanced Portfolio. The role will report into the SVP & Head of the Advanced Portfolio Unit and you will have direct line function responsibility for all Clinical Leads aligned to Hepatology medicines. It requires close partnering with leaders from within RIIRU and key cross‑functional partners across the organization. PLEASE NOTE: This career opportunity requires an on‑site office presence (minimum of two days a week) at one of GSK’s US sites (Upper Providence, PA or Waltham, MA). Key Responsibilities Lead building a portfolio of programs within the Hepatology TA that have clear potential for product differentiation, tractability in development and associated technical success probabilities that support clear investment decisions. Be accountable for the delivery of the full spectrum of advanced clinical development studies and submissions, Ph1b/2a through filing in hepatology. Be the single point of accountability for disease area strategy developed with input from internal GSK leaders & external academic thought leaders, research leads, regulatory authorities, investigators, and patient groups. Lead milestone transitions from candidate selection to filing/launch, guiding Clinical Leads on optimized strategies and alternative pathways to enable informed, strategic risk‑taking. Provide Medical Governance with specific accountability for managing and mentoring clinical staff in the disease area line and ensure proper training and compliance with internal and external policies, guidance, laws, and codes. Develop and maintain excellence in translational and clinical leadership in the disease area. Ensure the quality of clinical deliverables within the disease area including all documents and submissions including clinical data, through methods such as peer review, knowledge sharing/management, and standards and compliance. Function as Data Steward of the clinical data for the disease area (may include multiple assets), with oversight of breadth of disease data strategies and related data science efforts relevant to Hepatology TAs, to ensure activities are applied to benefit and impact of programs. Manage resourcing of clinical projects within the disease area across the assets in scope including portfolio projects and programs (encompassing early projects prior to candidate selection, through early and late‑stage clinical development) and business development/due diligence activities. Basic Qualifications Medical degree and clinical medical specialty board qualification in Gastroenterology, Hepatology or Endocrinology. Experience in (bio‑pharmaceutical) industry with experience in Hepatology or MASH clinical drug development. End‑to‑end clinical development experience including first‑in‑human trials & proof of mechanism, Ph2 (proof of concept), and Ph3 (registrational studies). Experience leading regulatory interactions and submissions (pre‑IND/IND, scientific advice, end‑of‑phase 2, pre‑NDA/BLA and files, advisory committee meetings). Experience in designing and executing clinical strategies. Experience leading projects that harness digital, technological, and statistical tools to support early‑stage programs in Hepatology. Experience in clinical safety and pharmacovigilance, with expertise in evaluation of safety signals and proactive risk management strategies. Experience with the local and global pharmaceutical industry, competitive landscape, revenue cycles and how end‑to‑end life operates. Preferred Qualifications Experience in navigating, influencing, and championing change in a large, complex, matrixed organization. Knowledge of advanced trial designs (adaptive and platform trials). Energized by delivering ambitious standards through collaboration and motivating others across the organization. Passionate about developing others into future leaders. Ability to think outside of conventional classifications of disease, where appropriate, and utilise cutting‑edge translational data (genetic, cellular, or systems biology) to support innovative translational strategies. Experience in leveraging expert knowledge for scientific, technical, clinical, and regulatory forward‑looking strategic thinking, problem solving and decision making in the evolving healthcare and digital data environments. Ability to balance short‑term needs with long‑term objectives to lead, resource and inspire teams and strategy according to portfolio priorities. Experienced and skilled people manager, influencer and disease visionary. Experience in stakeholder management skills across scientific, academic, regulatory, and political communities to identify and achieve mutual goals for the well‑being of patients and our communities. Benefits and Culture Why GSK? Unitinng science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, while creating an environment where our people can thrive and focus on what matters most. Equal Opportunity & Accommodation GSK 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. GSK: If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1‑877‑694‑7547 (US Toll Free) or +1 801 567 5155 (outside US). Notices GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies must obtain prior written authorization from GSK before referring any candidates. Please note that if you are a US Licensed Healthcare Professional, GSK may be required to capture and report expenses on your behalf, in compliance with federal and state US Transparency requirements. For more information, visit the Centers for Medicare and Medicaid Services website at https://openpaymentsdata.cms.gov/. #J-18808-Ljbffr
