Scientific Director, Oncology - Global Patient Safety

Role: Support safety strategy development and execution for AbbVie's oncology assets throughout their lifecycle, including due diligence activities. Responsibilities: translate nonclinical and clinical safety data into benefit-risk assessments, lead review and synthesis of safety documents (e.g., DSURs, RMPs, CSRs), facilitate cross-functional safety interactions, prepare competitive intelligence and disease landscape materials, support oncology due diligence, and drive safety process improvements. Qualifications: scientific or clinical degree (NP/PA, PharmD, MS, PhD, MPH), 5+ years in pharmacovigilance, clinical development, or biological sciences within pharma; strong expertise in oncology safety data interpretation, clinical trial methodology, and regulatory requirements; proven leadership and influence skills with excellent communication. High-Value: oncology, safety strategy, pharmacovigilance, clinical trial support, regulatory compliance, risk management, cross-functional collaboration. WorkSetup: not specified; likely hybrid or on-site based on typical roles.