Senior Medical Director – Hepatology

Set the clinical vision for the next generation of hepatology therapeutics.

We are seeking a Senior Medical Director with deep expertise in liver diseases to provide clinical leadership across our client’s expanding clinical development portfolio. This role offers the opportunity to lead clinical development programs with a primary focus on hepatology, while also supporting additional therapeutic areas as the pipeline evolves.

The position requires strategic oversight of clinical trials, close collaboration with cross‑functional teams, and meaningful engagement with external experts and regulatory authorities.

Applicants must have legal authorization to work in the United States.

Responsibilities:

• Serve as the clinical and strategic leader for assigned development programs, driving progress and quality
• Develop innovative yet practical clinical development strategies and support global regulatory approval pathways
• Oversee clinical trial conduct and safety, ensuring adherence to timelines and quality standards
• Provide strategic clinical input to research teams on development feasibility and proof‑of‑concept study design
• Collaborate closely with Preclinical, Regulatory Affairs, Biostatistics, Clinical Operations, Medical Affairs, Commercial, and Quality teams to ensure integrated development strategies
• Lead and supervise major clinical deliverables, including regulatory submissions, manuscripts, abstracts, and presentations
• Review and approve controlled documents such as clinical protocols, Investigator’s Brochures, and informed consent forms, in line with SOPs
• Represent clinical programs in external forums, including regulatory interactions, advisory boards, and scientific conferences

Key Skills and Requirements:

Education:

• MD or MD/PhD with a strong research background
• Board Certification or specialist training preferred

Experience

• 10+ years of industry experience, ideally in hepatology or related therapeutic areas
• Proven track record of leading Phase II-III clinical programs and engaging with Health Authorities

Skills

• Sound scientific and clinical judgment
• Expertise in clinical research, trial design, biostatistics, and regulatory guidelines
• Exceptional communication skills for presenting complex medical concepts
• Leadership and collaboration within a matrix environment
• Familiarity with biotech-pharma partnerships is a plus

Attributes

• Problem‑solving ability with balanced judgment
• Entrepreneurial mindset aligned with a culture of science, passion, and urgency

For more information, please contact Calum Watson.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

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