Join to apply for the Associate Director, Regulatory Affairs role at Mirum Pharmaceuticals, Inc.
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MISSION
Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and were looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.MISSION
Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and were looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously. Position Summary The Associate Director, Global Regulatory Affairs provides management of all aspects of assigned regulatory activities for the dedicated regions and related to the development and commercialization of novel liver drugs including quality, preclinical and clinical areas of drug development. This position will manage the timely delivery of regulatory applications by working with internal stakeholders and with corporate partners and distributors across multiple countries as assigned. The role is responsible for ensuring full regional regulatory compliance, and overseeing submissions and approvals of regulatory procedures including but not limited to IND, NDA, MAA, , and life cycle management activities. Job Functions/ResponsibilitiesReferrals increase your chances of interviewing at Mirum Pharmaceuticals, Inc. by 2x
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