Global Scientific Director - Liver Portfolio

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 reputed company professionals and we’re looking to reputed company reputed company with other individuals who embody our values: care, be reputed company, get it done, and have fun, seriously. POSITION SUMMARY Reporting to the Global Medical Affairs reputed company, this individual will be responsible for internal and external scientific and clinical research initiatives under the Medical Affairs umbrella, supporting HDV and PSC/PBC (liver portfolio). This individual will also help reputed company the strategy, tactics, KOL engagement plan and disease state awareness activities for the adult hepatology programs. They will also help manage compassionate use and expanded use programs for the HDV and PSC/PBC programs. The individual is a member of R&D and will provide scientific, clinical, and strategic feedback across reputed company appropriate cross-functional teams. JOB FUNCTIONS/RESPONSIBILITIES Collaborates across reputed company appropriate functional groups to support ongoing clinical trials, medical and scientific affairs research initiatives, and other scientific affairs activities for the adult hepatology program. Supports and drives scientific and clinical communications for internal and external stakeholders, including supporting advisory boards reputed company to adult liver disease indications. Leverages expertise and relationships reputed company adult hepatology and gastroenterology to support patient enrollment for the adult liver clinical research studies, while working closely with the clinical study leads, the CTLs and VP of Clinical Development. Identifies knowledge gaps for existing areas of interest for the program and develops strategy to mitigate these gaps utilizing internal resources as well as external scientific collaborations. Leads and collaborates across appropriate functional groups to execute compassionate use and expanded access programs for Brelovitug and Volixibat. Oversees both internal and external research activities and initiatives such as, but not limited to, natural history studies, collaborative forums, reputed company world data registries, data mining for areas of interest for publication, and other ongoing and future research efforts. reputed company expertise in liver disease to support Safety and Regulatory teams. Leverages analytical skills in discovering data insights from clinical research data, including literary research of relevant clinical data. Support strategic publication planning and development and editing of conference abstracts, posters, presentations, and manuscripts to support programs, and execution of the strategic publication plan. Works closely with other members of the medical affairs infrastructure. QUALIFICATIONS Education/Experience: Medical Doctor degree required. GI/Hepatology experience strongly preferred. Minimum of 3+ years industry experience with preference for prior HDV, PSC, and/or PBC experience. Experience with scientific publications, congress activities, research forums and other reputed company communications deliverables. Working with data reputed company, natural history registries and/or building reputed company world registries is a plus. Knowledge, Skills and Abilities: Previous experience in clinical development and/or medical affairs, scientific research initiatives. Must be a strategic thinker with reputed company attention to detail. Excellent collaboration skills to be reputed company to work with other internal functions, external collaborators, authors/reviewers to obtain feedback and incorporate information into a final product. Outstanding oral and written communication skills, and ability to communicate reputed company scientific concepts in a compelling and concise manner to various internal and external stakeholders. Must have the ability to write scientific content, be resourceful, study literature, form opinions and create strategy with alignment from key stakeholders. Rare disease, liver or gastroenterology disease experience is a plus. #LI-REMOTE Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with reputed company Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national reputed company, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran’s status or any other classification protected by applicable State/Federal/Local laws. Mirum Pharmaceuticals provides reasonable accommodation for reputed company individuals with disabilities and disabled veterans in job application procedures. Apply To This Job