Vice President, Pharmacovigilance and Drug Safety ( Head of Pharmacovigilance and Drug Safety)

Role: Lead global pharmacovigilance and drug safety for ORIC Pharmaceuticals' oncology portfolio, overseeing patient safety, safety surveillance, signal detection, and risk management in clinical development across phases 1-3. Responsibilities: develop and execute PV strategy, own safety assessments and regulatory submissions, ensure compliance, and establish inspection-ready PV systems. Serve as senior safety advisor to executive leadership, mentor PV team, and oversee vendor relationships. Qualifications: MD, PharmD, PhD, or equivalent; 12+ years in pharmacovigilance or clinical safety within biotech or pharma, with experience supporting investigational oncology products across phases. Deep knowledge of global PV regulations (FDA, EMA, ICH, GCP), proven leadership in PV operations, and regulatory interactions. Preferred: oncology drug experience, small molecule support, experience with regulatory submissions and post-market safety, and prior PV organization scaling in growth-stage biotech. Work setup: on-site in San Diego, salary range $310K-$385K; not H-1B eligible.