Scientific Director / Senior Medical Director, Medical Affairs - Global Oncology Pipeline (Prostate Cancer)

Role: Scientific Director / Senior Medical Director, Global Oncology Pipeline, focusing on prostate cancer. Objectives include providing medical and scientific input into strategic and operational activities, generating clinical data, and supporting educational and safety initiatives. Responsibilities encompass leading disease and asset strategies, overseeing evidence generation (including studies and collaborations), acting as a scientific interface with stakeholders, and developing medical narratives and communications for congresses and publications. Qualifications: PhD or PharmD with 10-15 years in pharma, including 7-10 years in Medical Affairs with global experience; extensive knowledge of prostate cancer therapeutics; familiarity with clinical trial methodology, data interpretation, and regulatory requirements; proven leadership in cross-functional teams; excellent communication skills. Senior roles (MD or equivalent) require 2+ years of clinical or medical affairs experience, with strong prostate cancer expertise preferred. High-value specifics include focus on prostate cancer, biologics or small molecules, phase 2-3 clinical activities, regulatory engagement, and global medical affairs strategy. The role interfaces with clinical development, commercial, and regulatory teams, with a hybrid work location (Mettawa, IL; Florham Park, NJ; South San Francisco, CA) and in-office Tuesdays through Thursdays.