ProPharma Hiring Pharmacovigilance Specialist: Life Sciences, B.Pharm, and Pharm.D Eligible

ProPharma, a global consulting partner specializing in regulatory sciences, clinical research, compliance, and life sciences solutions, is hiring for the position of Pharmacovigilance Specialist. The role involves managing end-to-end adverse event case processing, safety evaluations, and regulatory compliance across clinical trial and post-marketing portfolios.

Position Overview

Job Title: Pharmacovigilance Specialist
Organization: ProPharma
Experience Required: 2 years of relevant experience
Last Date to Apply: September 23, 2026

Key Responsibilities

Execute day-to-day processing of individual case safety reports (ICSRs) for clinical trial and post-marketed adverse events.
Perform medical coding using MedDRA, assess seriousness, and evaluate expectedness at both the event and case level.
Draft, structure, and review comprehensive case narratives.
Coordinate case follow-up procedures by identifying critical missing safety details.
Facilitate client communications and notifications related to ongoing case workflows.
Conduct peer quality checks to ensure data accuracy, consistency, and compliance with global pharmacovigilance regulations.
Escalate safety discrepancies or complex queries to the Principal PV Specialist or Case Processing Manager.

Eligibility & Qualifications

Education:
- Required: Bachelor’s degree in Life Sciences (including B.Pharm / B.Sc).
- Preferred: Advanced degree, Pharm.D, Registered Pharmacist (RPh), Registered Nurse (RN), or equivalent.
Core Competencies:
- Sound fundamental understanding of global safety guidelines and pharmacovigilance processes.
- Strong medical narrative writing and analytical problem-solving skills.
- High attention to detail with proven multitasking and case prioritization capabilities.