Medical Director, Hepatology Clinical Development (Hybrid)

Regulatory Jobs; Waltham (MA); Hybrid; USD 161,000 - 241,000; Full time

Job summary

GSK is seeking a Medical Director, Clinical Development with a strong focus on hepatology to provide clinical and scientific guidance across asset development from early concepts to registrational studies. You will collaborate with project teams to design trials, ensure safety, and support regulatory interactions.

The role sits within RIIRU, operates on a hybrid model with on-site presence required several days per week, and involves leading complex global studies and regulatory submissions.

Qualifications

• Medical degree required.
• Clinical medical specialty training with board qualification/registration in Internal Medicine or Primary Care / Family Medicine.
• Completion of a full clinical residency program leading to board qualification or certification.
• Experience working in the pharmaceutical industry in clinical drug development, with understanding of clinical trial execution from concept to publication.
• Direct experience with in‑stream medical oversight activities.

Responsibilities

• Lead clinical development activities up to registrational studies.
• Provide medical monitoring and oversight of patient safety during the study.
• Act as clinical lead for a study and be the clinical point of contact.
• Contribute to global regulatory submissions and briefing documents.
• Collaborate with cross-functional teams across disciplines to meet study milestones.

Skills

Medical degree

Clinical specialty training

Residency for board qualification

Pharma industry experience

Medical oversight activities

Job description

GSK is seeking a Medical Director, Clinical Development with a strong focus on hepatology to provide clinical and scientific guidance across asset development from early concepts to registrational studies. You will collaborate with project teams to design trials, ensure safety, and support regulatory interactions.

The role sits within RIIRU, operates on a hybrid model with on-site presence required several days per week, and involves leading complex global studies and regulatory submissions.