Remote Senior Pharmacovigilance Physician & Safety Lead

Merck; Salem (OR); Sur place; USD 282 000 - 444 000; Plein temps

Résumé du poste

Merck in Rahway, NJ is seeking a CSRM Physician to lead pharmacovigilance and risk management for assigned products. You will chair the Risk Management Safety Team and drive safety surveillance plans across development and post‑marketing stages, ensuring alignment with global pharmacovigilance strategies.

Responsibilities include safety data evaluation from trials, literature and post‑approval use; prepare safety summaries and regulatory documents; advise labeling and risk minimization actions,

Qualifications

• MD/DO or equivalent required; Board Certification preferred
• Minimum 3 years clinical experience post-training or relevant clinical experience
• Experience in drug development, clinical safety, pharmacovigilance or risk management
• Strong leadership, organizational and cross-functional collaboration skills
• Excellent written and verbal communication and analytical abilities

Responsabilités

• Lead safety surveillance and pharmacovigilance activities for assigned products
• Chair the Risk Management Safety Team and develop risk management plans
• Collaborate with clinical development, regulatory, epidemiology, statistics, and manufacturing teams
• Evaluate safety data from trials, literature, and post‑marketing use
• Prepare safety summaries and regulatory documents; advise on labeling and risk minimization

Connaissances

Pharmacovigilance

Clinical safety

Risk management

Leadership

Communication & writing

Formation

MD/DO or equivalent

Board Certification (preferred)

Description du poste

Merck in Rahway, NJ is seeking a CSRM Physician to lead pharmacovigilance and risk management for assigned products. You will chair the Risk Management Safety Team and drive safety surveillance plans across development and post‑marketing stages, ensuring alignment with global pharmacovigilance strategies.

Responsibilities include safety data evaluation from trials, literature and post‑approval use; prepare safety summaries and regulatory documents; advise labeling and risk minimization actions,