Clinical research physician - oncology

Experteer Overview You will apply your clinical and scientific expertise to drive late-stage oncology programs from development to market, collaborating across regional and global teams. In this role you influence clinical strategy, design trials, and oversee data dissemination while ensuring patient safety and regulatory compliance. You work with external thought leaders to advance science and support access and reimbursement strategies. This position offers global impact in breast cancer development within a mission-driven company. Retribuzione / Benefits Contribute to the clinical strategy, product lifecycle plans, and protocol design across regions and programs Draft and align clinical plans and value propositions with global and regional teams Design, conduct, and report local and global clinical trials, including sample size, timelines, and governance Review risk profiles and ensure ethical and regulatory compliance (GCPs, local laws) Identify investigators and oversee start-up activities, site training, and study initiation Monitor patient safety and follow up on adverse events per safety policies Support scientific data dissemination through publications, abstracts, posters, and communications Engage with regulatory agencies, external experts, and payer stakeholders to advance science and access Prepare and review regulatory submissions and labeling changes in collaboration with affiliates and regulatory teams Contribute to medical strategies to support brand commercialization and payer partnerships Lead or support education for medical personnel and cross-functional teams Stay updated on disease data, clinical practice trends, and competitive landscape Contribute to risk management and pharmacovigilance activities Represent Lilly in conferences, symposia, and advisory boards Responsabilità Medical Doctor with board eligibility or certification in a relevant specialty/subspecialty (US: board eligible/certified) Experience in international oncology practice For non-US trained physicians: LCME-compliant medical education Fluent in English (spoken and written) Knowledge of the drug development process Willingness to travel domestically and internationally per business needs #J-18808-Ljbffr