Global Pharmacovigilance (PV) Scientist, Senior Manager

About the role

For our client, we are seeking a Global Pharmacovigilance (PV) Scientist, Senior Manager to join the team of a leader in the Pharmaceuticals & Biotech space. This role will guide global drug safety activities with a strong emphasis on aggregate reporting, signal detection, and cross-functional safety oversight. The position partners closely with clinical development, affiliates, and decision-making teams to help ensure robust safety evaluation and timely communication of findings. It is well suited for a scientist who brings deep pharmacovigilance expertise, sound clinical judgment, and the ability to translate complex safety data into clear recommendations. The senior manager will also contribute to the design of safety data collection tools and support risk-informed oversight across clinical studies and product-related activities.

Location: Remote - US based candidates only, no visa sponsorship available

Responsibilities

• Direct planning and writing of aggregate reports
• Organize liaison activities with affiliates regarding products
• Support safety oversight in clinical trials by reviewing protocols and plans
• Review adverse events from clinical trials as required
• Participate in developing safety data collection forms for clinical studies
• Conduct data analysis to evaluate safety signals and document findings
• Prepare presentations for safety recommendations to decision-making teams

Qualifications

• Doctorate degree and 2 years of pharmacovigilance experience, or a master's degree and 4 years, or a bachelor's degree and 6 years, or an associate's degree and 10 years, or a high school diploma with 12 years of relevant experience
• Preferred BS in life science with 3 years of drug safety experience
• Experience in signal detection, evaluation, and management
• Literature surveillance skills and source document review knowledge
• Proficient in aggregate data analysis and interpretation
• Strong clinical and scientific judgment with medical research background
• Understanding of both qualitative and quantitative data analysis methods

Benefits

• Comprehensive benefits package including healthcare and life insurance
• Retirement and savings plan with company contributions
• Discretionary annual bonus program based on performance
• Stock-based long-term incentives for employees
• Award-winning time-off plans promoting work-life balance
• Flexible work models available where applicable

Pay

$140,799 – $190,492 annually