Remote CSRM Physician - Senior Pharmacovigilance Leader

Merck; Austin (TX); Remote; USD 282,000 - 444,000; Full time

Benefits offered by this job

Medical, dental, vision coverage

401(k) retirement plan

Paid holidays and vacation

Remote work flexibility

Job summary

Merck & Co., Inc. is seeking a CSRM Physician in Rahway, NJ to lead pharmacovigilance and risk management for assigned products.

You will chair the Risk Management Safety Team, guide safety strategy, and collaborate with clinical development, epidemiology, regulatory, statistics, and manufacturing to ensure global pharmacovigilance alignment. The role requires MD/DO or equivalent, 3+ years clinical experience, and strong leadership and communication skills.

Qualifications

• MD/DO or equivalent degree required.
• Board Certification preferred.
• Minimum of 3 years clinical experience following post-graduate training or relevant clinical experience.
• Experience in drug development, clinical safety, pharmacovigilance and/or risk management.
• Strong leadership, organizational, communication, writing and analytical skills.

Responsibilities

• Lead pharmacovigilance and risk management activities for assigned products.
• Chairs of the Risk Management Safety Team and develops pharmacovigilance plans.
• Collaborate with cross-functional teams to ensure safety in development and post-approval.
• Assess safety data from trials, literature, and real-world use; ensure complete safety information in core data sheets.
• Prepare safety summaries and regulatory documents; oversee safety data analyses.

Skills

Clinical Development

Clinical Risk Management

Clinical Safety

Pharmacovigilance

Regulatory Documents

Risk Management

Safety Assessment Reports

Drug Development

Drug Safety Surveillance

Excellent communication

Education

MD/DO or equivalent

Board Certification

Tools

MedDRA

Job description

Merck & Co., Inc. is seeking a CSRM Physician in Rahway, NJ to lead pharmacovigilance and risk management for assigned products.

You will chair the Risk Management Safety Team, guide safety strategy, and collaborate with clinical development, epidemiology, regulatory, statistics, and manufacturing to ensure global pharmacovigilance alignment. The role requires MD/DO or equivalent, 3+ years clinical experience, and strong leadership and communication skills.