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

- Solid English communication skills

Quality Review Associate (SME)

Experience: 2+ Years

Key Responsibilities:

- QC/Post-lock Case Processing Quality Review

- Review fatal and serious 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 (Bengaluru)
🏢 2COMs
📍 Bengaluru