Director, Medical Affairs (Cardiometabolic)

Arrowhead Pharmaceuticals•Pasadena, CA

2d•$230,000 - $260,000•Onsite

About The Position

The Director, Medical Affairs at Arrowhead Pharmaceuticals serves as the strategic and scientific lead for the cardiometabolic portfolio and is responsible for developing and executing Medical Affairs strategies for pipeline assets. This individual ensures the delivery of accurate, compliant, and scientifically rigorous medical guidance to both internal and external stakeholders. A core responsibility of this role is to serve as a key cross-functional partner to the Commercial organization, providing medical insight that informs strategy while upholding scientific integrity. Reporting to the Executive Director, Medical Affairs Strategy, this role plays a central part in shaping the scientific narrative, supporting launch readiness, and translating complex clinical data into meaningful insights that inform commercial strategy while preserving medical integrity. This is a full-time, onsite position at Arrowhead’s Corporate Headquarters in Pasadena, CA.

Requirements

Doctorate degree (PharmD or PhD) in life sciences, healthcare, or related field required
5+ years experience in Medical Affairs or related functions within the pharmaceutical or biotech industry with a strong understanding of Medical Affairs activities and strategy and compliance requirements.
Experience developing collaborative cross-functional relationships
Excellent organizational, project management, and communication skills.
Demonstrated ability to manage multiple projects simultaneously with strong attention to detail.

Nice To Haves

MD
Advanced training in lipidology, cardiometabolic disease, or rare/metabolic disorders

Responsibilities

In partnership with Medical Affairs Strategy Executive Director, develop and execute the comprehensive Medical Affairs strategy for pipeline molecules across the product lifecycle.
Translate clinical data, regulatory milestones, and competitive insights into a clear medical strategic plan.
Partner with Medical Communications on the development of scientific platforms, core data decks, and medical communication materials.
Identify evidence gaps and contribute to evidence generation planning in collaboration with Clinical Development and MVEO.
Contribute to the development of medical education initiatives related to zodasiran.
Support scientific exchange with external experts, as appropriate.
Assist in preparing medical content for advisory boards, speaker training, and scientific meetings.
Serve as the Medical Affairs partner with the Commercial Team.
Answer complex medical questions from Commercial, Market Access, and other internal stakeholders.
Help translate clinical and scientific data into insights that enhance field effectiveness while maintaining scientific integrity.
Participate in brand planning and launch readiness activities from a medical perspective.
Provide accurate, timely, and compliant medical guidance to inform promotional strategy and materials.
Review promotional materials for scientific accuracy and medical appropriateness.