Jobs at Mirum Pharmaceuticals

The Associate Director of GCP QA oversees GCP compliance for clinical studies, manages QA activities, and ensures adherence to regulations and quality standards.

Pre-launch regional account manager driving HDV disease-state awareness, screening, diagnosis pathways, and account readiness across Infectious Disease and community HBV providers. Builds KOL relationships, develops strategic account plans, strengthens referral networks, and collaborates cross-functionally to prepare markets for product launch.

Lead pre-launch disease-state education and account readiness for Hepatitis Delta Virus across infectious disease and community HBV providers. Build account plans, engage KOLs, establish referral pathways, collaborate cross-functionally, and drive HDV screening, diagnosis, and market activation while supporting launch readiness.

Lead pre-launch, disease-state education and account readiness for Hepatitis Delta Virus across Infectious Disease and community HBV providers. Drive HDV awareness, screening, referral pathways, KOL engagement, strategic account plans, cross-functional collaboration, and launch readiness in assigned territory.

Field-based, pre-launch regional account manager responsible for HDV disease-state education, account readiness, and market development across Infectious Disease and community HBV providers. Build account plans, engage KOLs, establish referral pathways, collaborate cross-functionally, assess launch readiness, and drive screening, diagnosis, and referral improvements. Frequent travel required to execute regional strategies.

Pre-launch regional account manager driving HDV disease-state awareness, screening, diagnosis, referral pathways, and account readiness across Infectious Disease and community HBV providers. Build KOL relationships, develop strategic account plans, collaborate cross-functionally to enable market development and launch readiness, and conduct frequent field travel to Southern California health systems and networks.

Pre-launch regional account manager driving HDV disease awareness, screening, and account readiness across infectious disease and community HBV providers. Build KOL relationships, develop account plans, strengthen referral pathways, collaborate cross-functionally, and assess launch readiness to establish diagnostic and referral infrastructure.

Regional Account Manager responsible for owning commercial strategy and execution for a liver product across South Carolina and Georgia. Build HCP relationships, drive awareness and access, develop territory business plans, analyze data to optimize growth, collaborate with cross-functional teams, ensure compliance, and support launches with ~60% travel.

Lead regional commercial efforts across Chicagoland, Wisconsin, and Minnesota to drive HCP awareness and uptake of Mirum’s liver product. Build KOL and interdisciplinary relationships, create and execute territory business plans, analyze data to optimize growth, ensure compliance, and collaborate with commercial, medical, and compliance teams. Requires frequent travel and focus on rare-disease market access and launch execution.

Second-line field leader driving zone commercial performance for a liver rare-disease portfolio. Builds and coaches Region Business Director teams, executes brand strategy, analyzes market dynamics, cultivates KOL relationships, partners cross-functionally, ensures compliance, and manages access and patient services while traveling frequently across a large multi-state territory.

Second-line field leader accountable for zone business performance across the liver portfolio. Build, coach, and develop four Region Business Director teams; translate national strategy into regional plans; drive execution and KPIs; analyze market trends; maintain KOL relationships; collaborate with cross-functional partners; support access and reimbursement navigation; and ensure compliance. Heavy travel required.

The Senior Director of Development Quality ensures GMP compliance for product development from early stages to commercialization, overseeing QA processes and regulatory submissions. This role requires extensive GMP knowledge and management experience.

The Associate Director manages program strategy, cross-functional planning, and ensures compliance with timelines and budgets for pipeline programs.

The AP Accountant processes accounts payable transactions, maintains vendor relations, ensures compliance, and supports financial audits in a dynamic environment.

The Senior Manager, Bioanalytical oversees bioanalytical studies for drug development, manages CRO collaborations, ensures regulatory compliance, and supports clinical submissions.

Field-based regional account manager responsible for developing and executing strategic regional business plans targeting geneticists, endocrinologists, and metabolic specialists. Drive diagnosis rates and sales growth, collaborate cross-functionally, manage multi-state territory, navigate rare disease patient journeys, and ensure compliance. Frequent travel required and strong presentation, analytics, and partner-management skills expected.

Regional Account Manager responsible for territory business ownership to drive HCP awareness and adoption of a liver portfolio product. Develop and execute go-to-market and account plans, build key thought-leader relationships, analyze business data to optimize growth, ensure compliance, collaborate cross-functionally, and support patient access. Role requires heavy travel and strong presentation, partner management, and scientific acumen in specialized disease areas.

Field-based regional role responsible for developing and executing strategic business plans to grow rare-disease therapy adoption across genetics, endocrinology, and metabolic specialists. Build customer relationships, improve diagnosis rates, support product launches, collaborate cross-functionally, manage large territory, and travel frequently to execute territory goals while ensuring compliance and patient-centric approaches.

Provide commercial legal counsel for marketing, sales, and commercial programs in a biopharmaceutical company. Draft and negotiate commercial agreements, support regulatory and compliance (FDA, OIG, transparency laws), advise on privacy (GDPR/CCPA), manage vendor and outside counsel relationships, and develop scalable legal policies and training across cross-functional teams.

This role leads the implementation and oversight of Veeva QMS modules, ensuring regulatory compliance and continuous quality improvements across multiple operations.