ICSR case processing || SPE/SME

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 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