Senior Medical Director - Hepatology
Hobsonprior
| Company | Hobsonprior |
| Category | Healthcare |
| Location | Cambridge, Massachusetts, USA |
| Remote | — |
| Employment | Not stated |
| Level | Director |
| Salary | Not stated by the employer |
| First seen | 3 Aug 2026 (the employer did not state a posting date) |
| Last verified | 11 Aug 2026 |
| Source | The employer's own careers page (company_site) |
Description
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• Senior Medical Director – Hepatology
This job is now closed.
Senior Medical Director – Hepatology
Reference: BBBH29109
Date posted: 11/05/2026
Job details
Specialism
Clinical Development
Expertise
Clinical/Medical Writing
Cambridge, Massachusetts, USA
Job type
Contract
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Description
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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Register your interest
If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.
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