Scientific Director, Oncology - Global Patient Safety

📋 Description

• Support the planning and execution of the safety strategy for Oncology assets during the entire
• Supports the Safety Leads and Product Safety Teams (PSTs) to translate nonclinical and clinical
• May lead development and implementation of an asset safety strategy with support of PST-L or
• Leads the review and synthesis of scientific safety data for critical regulatory and clinical
• Facilitate scientific connections and interactions, info exchange across assets within the safety
• Prepare material on competitive intelligence, current disease state and standard of care for key

🎯 Requirements

• Scientific or clinical degree (e.g. NP/PA, PharmD, MS, PhD, MPH, including combinations)
• 5+ years of experience in Pharmacovigilance / Clinical Development / Development biological
• Proven ability to critically evaluate and interpret complex safety data from oncology clinical
• Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical
• Ability to exercise judgment and address complex problems and create solutions across multiple
• Must be able to lead and manage through influence.

🎁 Benefits

• Comprehensive package of benefits including paid time off (vacation, holidays, sick)
• Eligible to participate in long-term incentive programs.