Global Pharmacovigilance Senior Scientist - Remote

Overview

The Global Pharmacovigilance Senior Scientist will contribute to safety assessment activities for medical/scientific operations, providing scientific and compliance expertise to Global Patient Safety.

In Short

• Direct planning and writing of aggregate reports.
• Organize liaison activities with affiliates regarding products.
• Support safety oversight in clinical trials.
• Review adverse events from clinical trials.
• Participate in safety data analysis and signal detection.
• Author safety assessment reports and regulatory responses.
• Assist in developing risk management strategies.
• Prepare presentations on safety recommendations.
• Support new drug applications and regulatory filings.
• Collaborate with cross-functional teams for safety activities.

Requirements

• Doctorate degree with 2 years of pharmacovigilance experience, or equivalent.
• BS or BA in Life Science preferred.
• Clinical/medical research experience.
• Experience in a biotech/pharmaceutical setting.
• Management or mentoring experience preferred.
• Strong analytical skills for data evaluation.
• Excellent communication skills.
• Ability to work collaboratively in a team environment.
• Familiarity with regulatory requirements for drug safety.
• Proficient in writing safety documents and reports.

Benefits

• Comprehensive employee benefits package.
• Retirement and Savings Plan with company contributions.
• Health, dental, and vision coverage.
• Life and disability insurance.
• Flexible spending accounts.
• Discretionary annual bonus program.
• Stock-based long-term incentives.
• Award-winning time-off plans.
• Flexible work models, including remote options.
• Career development opportunities.