Director/Senior Director, Scientific Affairs (Foster City)

Director/Senior Director, Scientific Affairs

Foster City

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 we’re looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously.

POSTION SUMMARY

Reporting to the Executive Director of Scientific Affairs, this individual will be responsible for internal and external scientific and clinical research initiatives under the Medical Affairs umbrella. This individual will also help develop the strategy, tactics, KOL engagement plan and disease state awareness activities for the adult hepatology programs.

The individual is a member of R&D and will provide scientific, clinical, and strategic feedback across all appropriate cross-functional teams.

JOB FUNCTIONS/RESPONSIBILITIES

• Collaborates across all 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 related to adult liver disease indications.
• Leverages expertise and relationships within 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.
• Oversees both internal and external research activities and initiatives such as, but not limited to, natural history studies, collaborative forums, real world data registries, data mining for areas of interest for publication, and other ongoing and future research efforts.
• Leverage 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.
• 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:

• Advanced degree in science; MD (preferred), PhD, or PharmD.
• GI/Hepatology experience strongly preferred.
• Minimum of 3+ years industry experience with preference for prior specific disease indication physician experience.
• Experience with clinical development strategic initiatives for enrollment of clinical studies.
• Experience with scientific and medical writing for regulatory documents, scientific publications, congresses, research forums and other core scientific communications deliverables.
• Working with natural history registries and/or building real 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 close attention to detail.
• Excellent collaboration skills to be able 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 complex 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-Onsite

Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, 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 qualified individuals with disabilities and disabled veterans in job application procedures.