Senior Director, Clinical Practice Liaisons
Madrigal PharmaceuticalsAbout the role
Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a liver disease with high unmet medical need. Madrigal’s medication, Rezdiffra (resmetirom), is a once-daily, oral, liver-directed THR-β agonist designed to target key underlying causes of MASH. Rezdiffra is the first and only medication approved by both the FDA and European Commission for the treatment of MASH with moderate to advanced fibrosis (F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment of compensated MASH cirrhosis (F4c).
The Sr. Director, Clinical Practice Liaison (CPL) is a key field-based leadership position responsible for the strategic and tactical oversight of the CPL team within a defined U.S. region. This individual will play a critical role in managing and developing CPLs, ensuring the team executes against the company’s medical strategy, complies with regulatory and internal policies, and delivers scientific value to both internal and external stakeholders.
This position will interface regularly and compliantly with cross-functional colleagues (e.g., Marketing, Sales, Market Access, Clinical Operations, HQ Medical Affairs) and external partners, including Thought Leaders (TL), healthcare decision-makers, and other relevant stakeholders.
Key Responsibilities
Team Leadership & Development
Recruit, coach, and manage performance of regional CPLs
Foster continuous development through mentoring and training
Align CPL activities with strategic objectives and tactical plans
Medical Strategy Execution
Drive implementation of regional field medical strategies
Translate national objectives into actionable, regionally tailored activities
Partner with cross-functional teams to integrate field insights into medical planning
Cross-functional Collaboration
Collaborate closely with Sales, Marketing, Market Access, and Clinical Operations
Serve as a field-based liaison for HQ Medical Affairs initiatives
Contribute to launch readiness and lifecycle management strategies
Clinical Trial Support
Collaborate with Clinical Operations to ensure successful study execution based upon recognized needs
Congress & External Engagement
Represent Medical Affairs at U.S. medical congresses in a compliant manner
Coordinate booth planning, scientific exchange, competitive intelligence, and post-conference debriefs
Strategic Team Building
Contribute to the design and structure of the U.S. Field Medical team
Identify evolving business needs and adjust regional capabilities accordingly
Compliance & Quality
Ensure all CPL activities comply with company SOPs, industry standards, and applicable regulations
Uphold the highest ethical standards in all external engagements
Travel Requirement
Willingness to travel 25–75% for congresses, site visits, and stakeholder engagement
Qualifications & Experience
Advanced degree in a scientific or healthcare discipline (MD, PharmD, PhD, DNP, etc.)
Minimum 5 years of Medical Affairs experience, including at least 3 years as an MSL or equivalent (translatable clinical practice experience will be considered)
Minimum 3 years of people management experience or formal leadership development participation
In-depth knowledge of clinical medicine and medical research; experience in cardiometabolic health, or MASH/NASH preferred
Proven ability to understand, communicate, and translate complex scientific information
Strong knowledge of U.S. healthcare system, FDA regulations, and medical affairs compliance standards
Demonstrated cross-functional collaboration, project execution, and strategic planning skills
Proficiency in Microsoft Office Suite, virtual communication platforms (e.g., Zoom), and CRM systems (e.g., Veeva)
Preferred Attributes
Strong interpersonal, presentation, and relationship-building skills
Adaptable and proactive in a fast-paced, evolving environment
Passion for
Apply for this role
Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.
Apply Now →Generate Application KitFree account required — sign up in 30s