We're Hiring | Pharmacovigilance – Case Processing Associate & Quality Review (SME)
Join our growing Pharmacovigilance team We're looking for experienced professionals with expertise in ICSR Case Processing and Quality Review.
Open Positions
Case Processing Associate (SPE)
Experience: 1–2 Years

Key Responsibilities:
Book-in and full data entry
Narrative writing / I-Narrative
Medical coding & Product coding
Self-check using Online QC Tool
Unblinding (if required)
Case routing
Case lock/closure (where applicable)
USPI labeling
Eligibility:
Graduate/Postgraduate/Doctorate in Life Sciences, Pharmacy, Medical Sciences, or equivalent
1–2 years of Pharmacovigilance Safety Case Processing experience
Hands-on experience with Veeva Safety and/or Argus Safety databases
Strong English communication skills

Quality Review Associate (SME)
Experience: 2+ Years

Key Responsibilities:
QC/Post-lock Case Processing Quality Review
Review fatal and responsible cases




Monitor and track daily quality metrics
Communicate quality findings to case processing teams
Identify errors and drive quality improvement initiatives
Ensure high-quality case processing deliverables
Eligibility:
Graduate/Postgraduate/Doctorate in Life Sciences, Pharmacy, Medical Sciences, or equivalent
2+ years of Pharmacovigilance Case Processing/Quality Review experience
Hands-on experience with Veeva Safety and/or Argus Safety databases
Strong English communication skills

Requirements

Relevant educational background and experience in patient safety or related field
Strong presentation and communication skills
Effective intercultural work capabilities
Commitment to timely completion of tasks and documentation
Analytical and problem-solving skills
Collaboration and teamwork abilities

📌 ICSR case processing || SPE/SME (India)
🏢 2COMs
📍 India