Senior Director, Global Medical Affairs Lead - Livmarli/Bile Acid Portfolio
In OfficeDirectorPharmaceuticalsExecutive DirectorChief Medical OfficerTeam ManagementBrand Strategy
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Requirements
- Advanced scientific or clinical degree (e.g., MD, DO, Pharm.D., PhD, PA, NP).
- Minimum of 2 years of management experience is required
- Experience supporting product development and/or launch preferred.
- Experience in generating a scientific communication strategy, including publications, symposia, advisory boards, medical education, etc.
- Rare disease experience and/or specialty therapeutic area experience preferred.
- Strong ability to understand, synthesize, and communicate complex scientific and clinical information.
- Demonstrated strategic thinking and leadership capabilities.
- Excellent oral, written, and presentation skills.
- Proven ability to work cross-functionally in a matrixed organization.
- Strong business acumen and understanding of drug development and commercialization.
- High level of professionalism, integrity, and compliance mindset
- Adhere and follow Mirum corporate values of “Be Real, Get it Done, Care and Have Fun Seriously.”
- The salary range for this position is $285,000 to $310,000 USD. Compensation will be determined based on several factors including, but not limited to; skill set, years of experience, and the employee’s geographic location. Please note that the required compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits unless otherwise provided.
- 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.
Responsibilities
- Global Medical Strategy & Leadership
- Lead the development of the Global Medical Affairs Plan (MAP), including strategic imperatives, medical objectives, tactics, evidence generation priorities, and scientific communication plans in collaboration with members of the Global Medical Affairs Team (GMAT) and aligned with the global brand plan.
- Provide global medical and scientific leadership for lifecycle management including launch and post-launch activities across regions.
- Ensure alignment with global brand strategy, clinical development plans, and regional medical needs.
- Lead, support and manage medical communications and publications including full-time employee(s) managing those initiatives.
- Evidence Generation & Data Strategy
- Collaborate with Scientific Affairs in evidence generation strategies, including real-world evidence (RWE), expanded access programs (EAP), Phase 3b/4 studies, observational research, externally sponsored research (ESR) programs, and HEOR initiatives.
- Partner with Clinical Development teams to ensure data generation addresses scientific, regulatory, and commercial needs.
- Oversee publication strategy and execution, ensuring quality, scientific rigor, and compliance with internal and external standards.
- Scientific & Medical Expertise
- Serve as the internal subject matter expert for the assigned therapeutic area or product.
- Interpret emerging scientific and clinical data and communicate implications to internal stakeholders.
- Maintain deep knowledge of disease state, treatment paradigms, competitive landscape, and clinical guidelines.
- External Stakeholder Engagement
- Lead a key global opinion leader (KOL) engagement strategy and ensure compliant scientific exchange with external experts.
- Partner with regional and local medical teams to coordinate steering committees, advisory boards, investigator meetings, congress activities, and scientific meetings.
- Lead medical education initiatives in collaboration with global and regional teams.
- Represent Medical Affairs in interactions with academic institutions, professional societies, and patient advocacy organizations.
- Cross-Functional Partnership
- Collaborate with Commercial, Clinical Development, Regulatory, Safety, Market Access, and HEOR to support integrated development and commercialization planning.
- Provide medical input into global brand plans, launch readiness activities, forecasting, and lifecycle management decisions.
- Support cross-functional teams with scientific insights, training, and medical review of materials.
- Compliance
- Ensure full compliance with company standard operating procedures (SOPs), regulatory requirements, and applicable laws and industry guidelines.
- Complete core compliance curriculum in a timely manner, as assigned by executive leadership
Benefits
- Collaboration with Scientific Affairs in evidence generation strategies
- Partnering with Clinical Development teams for data needs alignment
- Overseeing publication strategy and execution ensuring quality and compliance
- Leading a key global medical communications team, including managing full-time employee(s) responsible for these initiatives
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