Hepatology Clinical Development Lead

GSK; Greater London; Hybrid; GBP 120,000 - 180,000; Full time

Job summary

GSK seeks a Medical Director, Clinical Development, Hepatology to provide clinical insights for assets in liver disease. You’ll plan and execute development activities up to registrational studies, reporting to the Clinical Development Lead, driving clinical excellence and regulatory compliance across the program.

You will join the RIIRU unit and contribute to team-led research, external collaborations, and strategic execution, while ensuring patient safety and study integrity throughout the

Qualifications

• Medical degree and board-certified clinical specialty training.
• Experience in pharmaceutical clinical drug development and trial execution.
• Understanding of regulatory requirements and ICH guidelines.

Responsibilities

• Contribute to project teams planning indications and develop deliverables like TPP and CDP.
• Provide medical monitoring and oversight of trial safety with Pharmacovigilance.
• Lead clinical study design, protocols, and investigator brochures and CTAs.
• Engage with regulators and prepare briefing documents and responses.
• Oversee evidence generation and IES activities to support patient safety.
• Drive global regulatory submissions and strategic BD input.

Skills

Analytical Thinking

Business Acumen

Change Management

Clinical Research

Clinical Trial Designs

Communication

Decision Making

Fostering Collaboration

Influencing Without Authority

Leadership

Matrix Leadership

Mentorship

People Management

Risk Management

Strategic Thinking

Education

Medical degree

Board qualification/registration in Internal Medicine or Primary Care / Family Medicine

Completion of a full clinical residency program

Job description

GSK seeks a Medical Director, Clinical Development, Hepatology to provide clinical insights for assets in liver disease. You’ll plan and execute development activities up to registrational studies, reporting to the Clinical Development Lead, driving clinical excellence and regulatory compliance across the program.

You will join the RIIRU unit and contribute to team-led research, external collaborations, and strategic execution, while ensuring patient safety and study integrity throughout the