Global Pharmacovigilance (PV) Senior Scientist

Responsibilities

• Direct planning and review of aggregate reports
• Liaison with affiliates on product safety activities
• Author safety assessment and regulatory response documents
• Provide oversight for safety in clinical trials
• Conduct data analysis for safety signal evaluation
• Prepare materials for Health Authority Inspections
• Auxiliary in risk management strategy development

Qualifications

• Doctorate degree with 2 years experience or equivalent education and experience combination
• Preferred BS or BA in Life Science with MS and 6 years experience
• Experience in biotech/pharmaceutical setting (6 years)
• Prior managerial or leadership experience (2 years)
• Experience in clinical/medical research

Benefits

• Comprehensive employee benefits package
• Retirement and Savings Plan with company contributions
• Group medical, dental, and vision coverage
• Stock-based long-term incentives
• Flexible work models available where possible
• Award-winning time-off plans

Pay

• $140,799 – $190,492 annually

Schedule

• Remote - US based candidates only, no visa sponsorship available