Senior Director, Global Medical Affairs Lead

Mirum Pharmaceuticals•Foster City, CA

1d•$285,000 - $310,000•Hybrid

About The Position

The Director/Sr. Director/Executive Director, Global Medical Affairs Lead (GMAL) for the Hepatitis Delta program (HDV) is an internal medical affairs senior strategic leader responsible for shaping and executing the global medical strategy for the assigned therapeutic area or product. This role provides strong scientific leadership, evidence generation, external engagement, and cross-functional alignment to support successful product development, launch, and lifecycle management. The GMAL is the medical affairs strategic lead for an asset(s)collaborating closely with Scientific Affairs, Clinical Development, Marketing, Market access, Safety, and global regional medical teams to ensure alignment with global brand strategy and scientific priorities. This role will require both US and international travel at a minimum of 40-50%.

Requirements

Advanced scientific or clinical degree (e.g., MD, DO, Pharm.D., PhD, PA, NP).
Significant experience in Medical Affairs, with demonstrated global or regional leadership responsibilities.
Minimum of 2 years of management experience is required
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.”

Nice To Haves

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.

Responsibilities

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.
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.
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.
Lead global key 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.
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.
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