Mirum Pharmaceuticals is a biopharmaceutical company focused on developing and commercializing treatments for rare diseases, particularly those affecting children. The company has three approved medications: LIVMARLI® (maralixibat) for cholestatic pruritus in Alagille syndrome and progressive familial intrahepatic cholestasis (PFIC), CHOLBAM® (cholic acid) for bile acid synthesis disorders, and CTEXLI™ (chenodiol) for cerebrotendinous xanthomatosis. Mirum is also advancing a pipeline of investigational treatments, including Volixibat for primary sclerosing cholangitis and Fragile X syndrome, showcasing its commitment to innovative solutions in rare disease therapy.
Open Positions
Executive Director, Clinical Development
MD, 5+ years of experience in rare disease, knowledge of regulatory requirements
Manager, Commercial Operations Project Management
Bachelor's degree required. 3+ years of relevant project management or operations experience
Associate Director, GCP QA
Bachelor's degree in a scientific discipline, 10-12 years of experience, 5-10 years of GCP Quality experience, and 5+ years of supervising experience
Senior Manager, Commercial IT Integration Lead
6+ years of experience designing and supporting enterprise integrations in complex environments, with a strong focus on API-led design, event-driven patterns, and middleware platforms
Senior Manager, Commercial Supply Chain
6+ years of experience in global supply chain, supply chain planning, or related fields, with expertise in end-to-end commercial supply chain planning
Vice President, Nonclinical and Clinical Pharmacology
PhD or PharmD, 10+ years leadership experience, 15+ years drug development experience
Senior Director, Intellectual Property
JD/LLP & USPTO registration. 12+ years IP experience; in pharma, with US/EU/UK/J. Prof. degree in related field
Senior Director, Global Regulatory Affairs
15 years in pharmaceutical industry, 12 years in Global Regulatory Affairs, experience with major Health Authorities
Senior Manager, Clinical Pharmacology and Non-Clinical Sciences
BS in BioSci + 3+ yrs exp. Clinical PH. Strong PK/PD/PBPK/PBPK modelling & regulatory knowledge required. Experience with regulatory filings is a must
Senior Director, Regulatory Affairs CMC
At least 12 years of experience in Regulatory Affairs CMC, with a minimum of an advanced degree in a relevant scientific discipline
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