The Associate Director manages specialty pharmacy and IDN operations to drive patient access, adherence, and a high-quality prescriber experience. They collaborate with internal and external stakeholders to monitor vendor performance, ensure contractual compliance, and implement operational efficiencies.
The Thought Leader Liaison will cultivate and maintain commercial relationships with key opinion leaders to support the launch of Resmetirom. They are responsible for executing regional marketing initiatives, gathering market insights, and coordinating cross-functional engagement strategies.
The Key Account Director will drive the adoption of Rezdiffra by engaging with C-suite executives and medical directors within assigned Integrated Delivery Networks and HCP Super Groups. They are responsible for executing matrix business plans and fostering collaboration across cross-functional teams to ensure patient-centric solutions.
The Key Account Director will drive the adoption of Rezdiffra by engaging with C-suite executives and medical directors within assigned Integrated Delivery Networks and HCP Super Groups. They will execute effective pull-through programs and collaborate across matrix teams to develop patient-centric solutions and optimize business performance.
The Associate Director will develop and execute real-world evidence strategies to support global patient access and the commercial success of Rezdiffra. This role involves designing and conducting observational, pragmatic, and implementation science studies while collaborating with cross-functional teams to ensure high-quality evidence generation.
The Thought Leader Liaison will cultivate and maintain commercial relationships with key opinion leaders to advance brand and disease-state strategies for MASH. They will also lead regional congress planning, speaker management, and cross-functional collaboration to ensure market alignment.
The Area Business Manager is responsible for developing territory business plans to drive product adoption and achieve sales goals for Rezdiffra. They will build strategic relationships with healthcare professionals, provide clinical education, and collaborate with cross-functional teams to ensure patient access.
The Access and Reimbursement Manager serves as a field-based resource to support healthcare practices in navigating access barriers and reimbursement processes for specialty medications. They collaborate with internal teams and external stakeholders to ensure timely patient access to therapy through education and proactive problem resolution.
The Associate Director will partner with the Senior Director to develop the Clinical Monitoring Oversight program and manage an internal team of Clinical Research Associates. This role involves performing risk-based oversight activities, managing CRO relationships, and ensuring operational excellence across clinical trial sites.
The Regional Account Director will ensure formulary access to Rezdiffra across assigned regional payers while executing effective pull-through programs. They will collaborate with cross-functional teams to develop tactical plans and maintain deep expertise in the MASH disease state and market conditions.
Leads GMP API Quality Assurance and provides risk-based oversight of active pharmaceutical ingredient manufacturing across external CMOs/CDMOs. Manages API quality strategy, governance, and inspection readiness to ensure compliance with ICH Q7 and global health authority expectations.
Lead a regional team of Access and Reimbursement Managers to optimize patient access to specialty pharmacy products for healthcare providers. Develop and execute strategic plans to address reimbursement barriers and collaborate with internal stakeholders to ensure alignment.
Lead the execution and continuous improvement of the company's Compliance Program, focusing on project management and policy governance. Partner with legal and commercial stakeholders to implement scalable processes and ensure alignment with business objectives.
The Senior Director will provide strategic and operational quality oversight for global post-marketing pharmacovigilance and product quality complaint systems. They will lead cross-functional teams to ensure regulatory compliance, manage risk, and maintain inspection readiness across the product lifecycle.
The Executive Director oversees QMS process design, harmonization, and the operational excellence roadmap to ensure inspection-ready execution. They also lead the Quality KPI framework, manage quality event trending, and drive continuous improvement initiatives across the product lifecycle.
This position is responsible for ensuring the quality and compliance of Madrigal-sponsored clinical trials with GCP regulations and industry standards. Key duties include managing vendor quality, conducting audits, overseeing CAPA processes, and supporting inspection readiness activities.
