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
Director, Clinical Development
MD, PharmD, PhD or equivalent, ≥3 years of drug development, experience in Liver or rare disease a plus
Senior Specialist, Clinical Supply Chain
5+ years in pharmaceutical industry, 3+ years in Clinical Supply Chain, excellent planning and organizational skills
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
Director, GMP Quality Assurance Operations
8+ years of progressive cGMP Quality Assurance experience supporting biologics manufacturing and analytical testing in a regulated environment
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
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
Executive Director, Clinical Development
MD, 5+ years of experience in rare disease, knowledge of regulatory requirements
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