Associate Director, Global Medical Information

Role: Associate Director of Medical Information within Medical Affairs, supporting the delivery of accurate, evidence-based responses to HCPs, patients, and caregivers throughout the product lifecycle. Responsibilities: develop and maintain Medical Information resources, handle unsolicited inquiries, monitor scientific trends, support congress activities, and collaborate with cross-functional teams including Medical Affairs, Clinical Development, and Regulatory to ensure compliant, up-to-date communication. Requirements: advanced degree in a scientific or medical field (PharmD, MD, PhD), 8+ years supporting Medical Information or Medical Affairs in biotech/pharma, experience with regulatory compliance, excellent communication skills, proficiency with medical content management systems (preferably Veeva PromoMats), and ability to manage multiple priorities. Preferred: oncology therapeutic area experience, launch support background, and familiarity with clinical data and publications. HighValue: oncology, supporting RAS-addicted cancers, product lifecycle management, regulatory compliance, and cross-functional scientific collaboration. WorkSetup: hybrid or onsite in Redwood City, CA, with 10-20% travel.