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Pharmacovigilance Associate

0-2 years
Not Disclosed
10 Feb. 10, 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

Pharmacovigilance Associate

PrimeVigilance | Full-time | Drug Safety | ICSR Processing

PrimeVigilance is seeking a Pharmacovigilance Associate to join its Individual Case Safety Report (ICSR) team, offering a great opportunity to start and develop a career in Drug Safety.

Key Responsibilities

  • Process Individual Case Safety Reports (ICSRs) in compliance with regulations, PrimeVigilance SOPs, and client-specific requirements.
  • Perform ICSR follow-ups to ensure complete and accurate reporting.
  • Handle Product Quality Complaints (PQC) and collaborate with Quality Assurance.
  • Perform MedDRA and WHO coding for adverse event classification.
  • Communicate with other departments (Quality, Medical Information) as required.

Qualifications & Skills

  • Degree in Life Sciences / Biomedical field (e.g., Chemistry, Biology, Biotechnology, Veterinary Science).
  • Strong time management, multitasking, and organizational skills.
  • Attention to detail and ability to work under tight deadlines.
  • Excellent interpersonal and communication skills.
  • Advanced English proficiency (B2 or higher, verbal and written).
  • Additional language skills are an advantage.
  • Proficiency in MS Office (Word, Excel, PowerPoint).

📍 Location: Remote/Hybrid
Start Date: ASAP