Associate Director, Medical Information

About Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunctionassociated steatohepatitis (MASH), a liver disease with high unmet medical need. Madrigal’s medication, (resmetirom), is a once-daily, oral, liver-directed THR-β agonist designed to target key underlying causes of MASH. This 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 (resmetirom) for the treatment of compensated MASH cirrhosis (F4c). Position Summary Reporting to the Executive Director, Medical Information, the Associate Director, Medical Information will be responsible for the generation, revision, review and maintenance of frequently asked questions, standard response letters and custom inquiries for use in response to unsolicited requests for both approved and investigational products for Madrigal Pharmaceuticals. The AD, Medical Information will also provide cross-functional support in execution of departmental deliverables. The AD, Medical Information will also support the medical review for promotional and medical materials. The AD, Medical Information will remain current on relevant medical/scientific therapeutic areas of interest to the company and professional standards to ensure they are able to provide timely, accurate, balanced and compliant medical information. Key Responsibilities Support the Global Medical Information and local European markets operational strategies/objectives and provide medical, scientific and technical support for the Madrigal Pharmaceuticals product portfolio and/or products under clinical development Support project plans that ensure pre- and post- product launch preparedness of the Medical Information department, including support of Medical Information Call Center, Medical Affairs, Medical Science Liaisons, Payer, and Commercial teams Provide quality review for inquiry handling by Medical Information Call Center, provide input for efficient inquiry handling/triage, and overall dissemination of scientific information Provide literature search/evaluation, writing, management and review support for the development of medical information resource documents (Standard Responses and FAQs) and in the handling of medical information requests for assigned products and therapeutic areas Respond verbally and in writing to escalated and custom responses from the Medical Information Call Center Support Medical Information congress activities, including face to face attendance and Medical Information booth coverage Ensure all medical information content is scientifically developed and maintained to ensure current/relevant data is disseminated upon request Train Medical Information Call Center agents and Medical Affairs colleagues on Medical Information content Act as Medical Reviewer for promotional and medical content, including data check and reference requirements to ensure medical accuracy of both promotional and non-promotional materials as required Support the technology needs across the Medical Information function Contribute to submission(s) of compendia listings Contribute to the development of Medical Information processes and SOPs Liaise with Medical Affairs to identify emerging medical information content needs and insight analysis Follow the vision and strategy to enhance or create channels for responding to unsolicited requests for medical information or communicating key scientific information about our products Qualifications Required: Advanced scientific degree (e.g., PharmD, PhD) is required with a minimum of 6+ years within the pharmaceutical industry; minimum of 4+ years of medical information experience within the pharmaceutical industry Demonstrated ability to work with cross functional teams is required Preferred: Experience with Medical Inquiry and document management systems, Standard Response writing/management, launch experience, medical review of medical and promotional material, significant knowledge of relevant global, national, and regional regulations and codes of practice (ABPI, EFPIA, IFPMA-AIFD), and GDPR requirements. Fluent in German and English Willingness to travel to international conferences Additional Information 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.