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Senior Medical Director, Clinical Development, Advanced Pipeline Unit; APU), Hepatology

Job in Collegeville, Montgomery County, Pennsylvania, 19426, USA
Listing for: Women In Bio
Full Time position
Listed on 2026-01-26
Job specializations:
  • Healthcare
    Medical Imaging
Job Description & How to Apply Below
Position: Senior Medical Director, Clinical Development, Advanced Pipeline Unit (APU), Hepatology

Senior Medical Director, Clinical Development

Advanced Pipeline Unit (APU) – Hepatology

Location:

Collegeville, Pennsylvania, United States (on‑site, minimum two days per week)

Posted:
Jan 22 2026

GSK is seeking a highly skilled Senior Medical Director, Clinical Development for an Advanced Pipeline Unit (APU) Hepatology group to provide clinical and scientific leadership for potential new, established, and emerging indications for assets in clinical development with a strong focus on steatotic liver disease (SLD), including alcohol‑associated liver disease (ALD). The role reports to the Senior Director/Clinical Development Lead for an SLD therapeutic area and is pivotal in driving GSK’s mission to deliver transformative medicines to patients, ensuring clinical excellence, regulatory compliance, and operational efficiency.

About

RIIRU

The Respiratory, Immunology and Inflammation Research Unit (RIIRU) was formed in 2024 to identify and advance novel molecular targets with genetic associations to disease based on the foundational observation that targets with human genetic evidence improving clinical success by two‑fold. RIIRU’s remit is to identify novel targets, develop assets for clinical studies, and perform trials through to regulatory submission, enabled through strategic external and GSK‑internal partnerships.

Key Responsibilities
  • Contribute to the clinical development strategy for a drug or program.
  • Ensure execution of clinical development plans (CDP) for product(s) and/or indication(s) and provide strategic oversight and management of clinical trials.
  • Lead clinical development activities from a therapeutic area and clinical trial perspective, including:
    • Provide clinical and medical oversight of ongoing clinical trials.
    • Lead clinical trials and asset‑level activities in a matrix team structure.
  • Identify and highlight transformational opportunities that offer highly significant benefit to patients.
  • Contribute to the development of the Integrated Evidence Strategy (IES). Integrate scientific rationale, regulatory requirements, product development plans, and commercial goals to optimize asset indications and trials.
  • Contribute to clinical development discussions and teams at global regulatory interactions. Draft clinical components of global regulatory submissions/files (e.g., IND, NDA, BLA, MAA), including briefing documents, presentations, and responses to regulatory questions.
  • Promote innovative methodologies and processes, including digital tools, encouraging others to think differently and adopt new ways of working.
  • Stay abreast of advancements in therapeutic area research, clinical trial methodologies, competitive environment, and regulatory space to maintain GSK’s competitive edge.
Basic Qualifications
  • Medical degree and clinical medical specialty training board qualification/registration in Internal Medicine or Primary Medical.
  • Experience in the global pharmaceutical/biotechnology industry in the field of Hepatology.
  • Experience in clinical research and drug development, with a focus on SLD, including ALD and MASH.
  • Experience in late‑stage Hepatology drug development, including Phase 2 and Phase 3 clinical trial design, initiation, execution, and closure.
  • Experience in medical monitoring activities and oversight.
  • Experience in leading regulatory submissions and managing global clinical trials.
  • Experience with ICH and GCP guidelines and regulatory requirements.
  • Matrix team experience within a clinical development setting.
Preferred Qualifications
  • Medical degree and clinical medical specialty board qualification/registration in Hepatology/Gastroenterology, Endocrinology, or Nephrology.
  • Thorough understanding of SLD, including ALD and MASH, the underlying biology and potential therapeutic targets.
  • Solid understanding of needs and priorities of regulators, payers, and prescribers in relevant global markets.
  • Track record of building and maintaining strong relationships with internal and external stakeholders.
  • Demonstrated strong problem‑solving skills and innovative thinking; anticipation of potential challenges, strategic approach development, and effective communication of uncertainty.
  • Enterprise mindset;…
Position Requirements
10+ Years work experience
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