Sr. Process Executive - PharmacoVigilence ICSR Case Processing

About the Client:

Join our growing Pharmacovigilance team! We're looking for experienced professionals with expertise in ICSR Case Processing and Quality Review.

Open Positions

SPE – ICSR / Pharmacovigilance

Key Responsibilities:

• Manage end-to-end ICSR case processing, including intake, triage, data entry, follow-up and case closure.
  

• Perform MedDRA/WHO Drug coding, narrative writing and case assessment as per SOPs and regulatory requirements.
  

• Ensure accurate and timely processing/submission of serious and non-serious ICSRs within defined timelines.
  

• Maintain high standards of data quality, compliance and documentation across the case lifecycle.
  

• Support reconciliation, quality checks and resolution of case-related queries or discrepancies.
  

Required Skills:

• 1–4 years of relevant Pharmacovigilance / Drug Safety / ICSR experience.
  

• Hands-on experience in ICSR case processing.
  

• Strong understanding of PV processes, regulatory timelines and safety case lifecycle.
  

• Argus and/or Veeva Safety experience preferred.
  

• Graduate/Postgraduate in Pharmacy, Life Sciences, Medical Sciences or a related discipline.
  
  

Requirements

Joining Preference: Immediate to 30 Days highly preferred. 90-day notice period candidates will not be considered.