Senior Post-Market Pharmacovigilance Specialist

Job overview

The Senior Post-Market Pharmacovigilance Specialist role is fully remote; compensation is not specified. MMS is a clinical research organization supporting pharmaceutical, biotechnology, and medical-device industries with clinical data and regulatory submission services. The specialist leads post-marketing safety case processing, maintains related workflows, and supports regulatory compliance and client deliverables. The work helps ensure drug-safety information is processed accurately and in accordance with applicable guidance and procedures.

What you'll do

• Lead global post-marketing case processing from intake through reporting and closure
• develop and maintain pharmacovigilance workflows and procedures
• ensure compliance with GVP, FDA requirements, and company SOPs
• process cases and lead high-quality deliverables
• provide strategic narrative development and client support
• manage client meetings and project work
• mentor colleagues and identify process efficiencies.

What we're looking for

Skills & competencies

senior pharmacovigilance specialist

post-market safety

drug safety

case processing

pharmacovigilance

gvp

fda compliance

clinical research

fully remote

mms

client projects

meddra

Work arrangement

• Weekend coverage required

Why this role

Fully remote role; the posting notes that final title and scope will be determined based on the successful candidate’s experience, background, and qualifications.

About the employer

MMS is hiring for this role. Industry: Testing Laboratories and Services. Sector: 54.