Senior Director, Clinical Operations

Company Overview

Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality. Every member of our Madrigal team is connected by our shared purpose: leading the fight against MASH. 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). Our success is driven by our people. We are building a dynamic, inclusive, and high-performing culture that values scientific excellence, operational rigor, and collaboration.

To support our continued growth, we are strengthening our workforce strategy to ensure we have the right talent, at the right time, in the right way.

The Senior Director, Clinical Operations provides strategic and operational leadership for the planning, execution, and oversight of global Phase I-IV clinical trials and clinical development programs. This role is accountable for the successful delivery of one or more complex clinical programs from study start-up through closeout, ensuring execution against timelines, quality, budget, and corporate objectives while maintaining compliance with global regulatory requirements.

The Senior Director, Clinical Operations will drive operational strategy across a portfolio of studies while partnering closely with Clinical Development and cross-functional leadership to support the Company’s development objectives. This individual provides organizational leadership, line management, and mentorship to Clinical Operations staff, while building scalable processes and operational excellence within a rapidly growing biotechnology environment.

• Provide strategic and operational leadership across one or more global Phase I-IV clinical development programs.
• Provide portfolio oversight to ensure studies are executed according to corporate priorities, development milestones, quality standards, timelines, and budgets.
• Lead operational planning and execution of complex clinical trials from study start-up through closeout.
• Develop robust operational strategies and accelerated delivery plans to support corporate development objectives.
• Embrace an ownership mindset by proactively identifying, assessing, managing, and communicating operational risks impacting study and program delivery.
• Accountable to ensure trials are conducted in compliance with ICH-GCP, FDA, EMA, and applicable regional regulations.
• Lead CRO selection, contracting, and ongoing oversight for responsible trials.
• Serve as the primary operational liaison with CROs and key vendors.
• Monitor CRO and vendor performance through key performance indicators, governance meetings, quality metrics, timelines, budgets, and operational deliverables.
• Drive proactive issue resolution and risk mitigation across CROs, vendors, and internal stakeholders.
• Represent Madrigal during investigator meetings, Site Initiation Visits, governance meetings, and key external interactions, maintaining a patient-focused approach.
• Partner with Clinical Development and cross-functional teams to influence operational aspects of protocol development, study design, feasibility assessments, and execution strategies.
• Provide strategic oversight for study-related documents including operational plans, monitoring plans, site manuals, project tools, informed consent forms, and other essential trial documentation.
• Provide operational leadership supporting INDs, CTAs, protocol amendments, investigator brochures, and other global regulatory submissions.
• Lead and manage trial level meetings and deliverables.
• Develop and oversee global site identification, feasibility, activation, enrollment, and retention strategies.
• Collaborates with data management in the design, format and content of CRFs, study guides, study reference binders, patient diaries, and forms including participating in the EDC and IVRS specification process and UAT.
• Ensure timely resolution of CRF queries through collaboration with CROs, Clinical Data Management, and study teams.
• Coordinate and oversee Investigational Product including overall accountability and reconciliation.
• Manage and/or oversee study budget and payment process for all clinical trial vendors including investigative sites.
• Provide strategic oversight of all clinical trial vendors including central laboratories, imaging vendors, ECG providers, IRT, eCOA, IRBs, and specialty vendors.
• Partner closely with internal partners such as Clinical Development, Regulatory Affairs, Data Management, Project and Portfolio Management, Biostatistics and Data…