Senior Pharmacovigilance Physician (Remote, U.S.)

Job overview

The Senior Pharmacovigilance Physician role is remote in the United States. Compensation is not specified. MMS is a clinical research organization supporting pharmaceutical, biotech, and medical device companies with clinical trial data and regulatory submission work. The physician independently manages complex medical-review assignments, applies medical judgment to safety issues, and supports compliant signal management and safety surveillance. The role also contributes medical expertise to client discussions, safety deliverables, and the development of other reviewers.

What you'll do

• Manage signal management and safety surveillance activities
• perform and oversee signal detection
• represent the company in internal and external safety interactions
• interpret regulations and guidance
• review safety deliverables and individual case safety reports
• code clinical data using MedDRA and WHO Drug
• review aggregate safety reports and cumulative safety data
• manage client meetings and feedback
• identify project risks
• mentor others in medical review and pharmacovigilance.

What we're looking for

Skills & competencies

senior pharmacovigilance physician

remote u.s.

medical review

safety surveillance

signal detection

pharmacovigilance

meddra

who drug

clinical research

mms

md or do required

aggregate safety reports

Work arrangement

• Weekend coverage required

Why this role

MD or DO required; board certification preferred. Requires at least five years of pharmacovigilance, safety signal detection, aggregate report review or authoring, or similar experience.

About the employer

MMS is hiring for this role. Industry: Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology). Sector: 54.