Senior Pharmacovigilance Physician - Global Safety Lead

Evestia Clinical Group; Union (NJ); Hybrid; USD 180,000 - 230,000; Full time

Benefits offered by this job

Flexible working

Professional growth

Job summary

Evestia Clinical Group is seeking an experienced Pharmacovigilance Physician to provide medical leadership and oversight of safety data for investigational and marketed products. You will review IC SRS, assess causality and seriousness, and contribute to post-market safety reporting.

You will collaborate with Medical Affairs and monitoring teams to ensure safety and benefit-risk assessment across programs, while mentoring PV staff and supporting regulatory inquiries.

Qualifications

• MD/DO/MBBS or equivalent required.
• Active or previously held medical license/registration required.
• Minimum 2 years of physician experience in pharma/CRO focusing on pharmacovigilance and drug safety.
• Hands-on experience with medical review of ICSRs and knowledge of global safety regulations.

Responsibilities

• Lead medical review of safety data from clinical trials and post-marketing projects, including causality and seriousness assessments.
• Review MedDRA and WHO Drug coding for adverse events and concomitant medications.
• Author medical assessments, summaries and safety-related queries to sites or reporters.
• Provide medical oversight for periodic safety reports (PBRERs, PSURs, DSURs) and regulatory responses.
• Support PV team through mentoring and training; contribute to signal detection and risk management activities.

Job description

Evestia Clinical Group is seeking an experienced Pharmacovigilance Physician to provide medical leadership and oversight of safety data for investigational and marketed products. You will review IC SRS, assess causality and seriousness, and contribute to post-market safety reporting.

You will collaborate with Medical Affairs and monitoring teams to ensure safety and benefit-risk assessment across programs, while mentoring PV staff and supporting regulatory inquiries.