Madrigal Pharmaceuticals

Title: Senior Director, Clinical Practice Liaison

Location: Texas, United States

Base: Base salary determined by qualifications, skills, education, experience, business needs, and market demands; may be eligible for bonus, equity, and comprehensive benefits

Bonus: Eligible for bonus and equity

Summary

The Senior Director, Clinical Practice Liaison leads and manages a regional CPL team to execute medical strategies and ensure compliance with regulatory and internal policies. The role involves collaboration with cross-functional teams including Marketing, Sales, Market Access, Clinical Operations, and Medical Affairs, supporting clinical trials, representing Medical Affairs at congresses, and contributing to strategic planning and team building. Requires an advanced scientific or healthcare degree (MD, PharmD, PhD, DNP), medical affairs experience, leadership skills, and knowledge of clinical medicine and medical research.

Added on: 07/16/2025

Full Job Description

Madrigal is a biopharmaceutical company pursuing novel therapeutics for non-alcoholic steatohepatitis (NASH), also known as metabolic dysfunction associated steatohepatitis (MASH). Our first therapy, Rezdiffra (resmetirom), was granted accelerated approval by the U.S. Food and Drug Administration (FDA) for the treatment of adults with NASH with moderate to advanced liver fibrosis (consistent with stages F2 to F3 fibrosis) and is being studied in a Phase 3 trial for the treatment of NASH with compensated cirrhosis.

Title: Sr. Director, Clinical Practice Liaison (CPL)

Role Summary

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 mentoring, team building, and field-based medical innovation

Compensation: Base salary is determined by several factors that include, but are not limited to, a successful candidate's qualifications, skills, education, experience, business needs, and market demands. The role may also be eligible for bonus, equity, and comprehensive benefits, which include flexible paid time off (PTO), medical, dental, vision, and life and disability insurance.

Madrigal is an Equal Opportunity Employer. All employment is decided on the basis of qualifications, merit, and business need. Applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex gender identity, sexual orientation, national origin, age, disability, protected veteran or disabled status, or other characteristic protected by applicable federal, state, or local law.

Unsolicited resumes from agencies should not be forwarded to Madrigal. Madrigal will not be responsible for any fees arising from the use of resumes through this source. Madrigal will only pay a fee to agencies if a formal agreement between Madrigal and the agency has been established.

Please be aware that we are currently receiving numerous reports of individuals misrepresenting themselves as Madrigal Pharmaceuticals’ Hiring Managers, seeking to engage with job candidates through fraudulent online advertisements or job posting sites. These unauthorized individuals are using Madrigal’s name and logo in an attempt to solicit up-front fees and obtain personal information from interested job candidates. Please know that Madrigal does not conduct interviews via text or in chat rooms; conduct interviews via Skype, RingCentral or solely via telephone; charge candidates an advance fee of any kind (e.g., fees for purchasing equipment); nor does it offer positions of employment without undergoing a thorough recruiting process. Interviews with Madrigal are conducted via the Zoom platform.

Please also note that any correspondence with regard to employment would come from an authorized madrigalpharma.com email address or from an email address from one of our trusted search firm partners. We are aware that incorrect/fraudulent email addresses, with Madrigal misspelled, have been utilized in these most recent fraud attempts. If you receive unsolicited employment offers from people claiming to work for Madrigal we recommend that you: do not respond to their questions; do not open any attachments; and do not click on any hyperlinks.