Senior Pharmacovigilance Physician & Risk Lead

Merck; Trenton (NJ); À distance; USD 282 000 - 444 000; Plein temps

Avantages offerts par ce poste

Annual bonus

Long-term incentive

Medical, dental, vision insurance

401(k) retirement benefits

Résumé du poste

Merck in Rahway, NJ is seeking a CSRM Physician to lead pharmacovigilance, risk management and safety surveillance for investigational and marketed products. The role chairs the Risk Management Safety Team and guides safety strategy across cross-functional teams.

The position requires MD/DO (or equivalent), 3+ years post-graduate clinical experience, and strong skills in pharmacovigilance, risk management, and regulatory documentation. Remote work options may be available.

Qualifications

• MD/DO or equivalent required.
• Board certification preferred.
• Minimum of 3 years clinical experience following post-graduate medical training or other relevant clinical experience.
• Experience in drug development and pharmacovigilance.

Responsabilités

• Lead pharmacovigilance and risk management planning as chair of the Risk Management Safety Team.
• Collaborate with cross-functional teams to ensure safety assessment and regulatory compliance.
• Perform safety data evaluation from clinical trials, literature, and post-approval use.
• Prepare safety summaries and analyses for regulatory documents.
• Oversee labeling reviews and use of MedDRA.
• Develop standards, processes, metrics and initiatives for the department.

Connaissances

Clinical Development

Clinical Risk Management

Clinical Safety

Clinical Training

Drug Development

Drug Safety Surveillance

Pharmacovigilance

Regulatory Documents

Risk Management

Safety Assessment Reports

Formation

MD/DO or equivalent

Board Certification

Description du poste

Merck in Rahway, NJ is seeking a CSRM Physician to lead pharmacovigilance, risk management and safety surveillance for investigational and marketed products. The role chairs the Risk Management Safety Team and guides safety strategy across cross-functional teams.

The position requires MD/DO (or equivalent), 3+ years post-graduate clinical experience, and strong skills in pharmacovigilance, risk management, and regulatory documentation. Remote work options may be available.