New Jersey Licensed Senior Scientist

Job Summary

A company is looking for a Senior Scientist in Global Drug Safety & Pharmacovigilance.

Key Responsibilities

• Lead project management activities for aggregate safety reports and ensure on-time submissions
• Perform quality control of aggregate safety reports to ensure regulatory compliance and scientific integrity
• Develop and maintain standard operating procedures, templates, and training materials for pharmacovigilance processes

Required Qualifications

• Advanced degree in life sciences or related field
• Experience in pharmacovigilance and aggregate safety reporting
• Strong understanding of regulatory requirements for safety reporting
• Proven project management skills in a pharmaceutical or biotech environment
• Experience in medical writing and quality control processes