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Pharmacovigilance Aggregate Report Writer

5-6 years
₹8 – ₹14 LPA
10 June 14, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Pharmacovigilance Aggregate Report Writer
Location: New Delhi (Work from Office)

Job Summary:
An immediate opening is available for a Pharmacovigilance (PV) professional with 5–6 years of dedicated experience in aggregate report writing. This role strictly excludes ICSR experience and focuses solely on candidates who have hands-on expertise in preparing and managing aggregate safety reports such as PSURs, PBRERs, DSURs, and other regulatory safety documents.

Key Requirements:

  • Experience: 5–6 years in Pharmacovigilance aggregate report writing

  • Mandatory: Prior experience only in aggregate reportingICSR experience will not be considered

  • Location: New Delhi (On-site, not remote or hybrid)

  • Join Immediately or Short Notice Preferred

Application:
If you meet the above criteria, share your updated resume at
vashistha.mohit@gmail.com.
Please apply only if your experience is in aggregate report writing.

Estimated Salary Range: ₹8 – ₹14 LPA (based on role and experience)