SSI People
SSI People

Pharmacovigilance (PV) Specialist / Drug Safety Case Processing Specialist/Clinical Trial Consultant

Remote • Posted 5 hours ago • Updated 5 hours ago
Contract W2
6 Months
No Travel Required
Remote
$60/hr
Fitment

Dice Job Match Score™

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Job Details

Skills

  • Pharmacovigilance
  • ICSR
  • QC
  • Argus
  • ArisG
  • veeva
  • MedDRA coding

Summary

Job Description:
Responsible for processing and quality checking (QC) of clinical trial and post-marketing Individual Case Safety Reports (ICSRs). Key responsibilities include case intake, triage, data entry, MedDRA coding, narrative writing, follow-up queries, case reconciliation, and ensuring timely regulatory reporting in compliance with global pharmacovigilance regulations.

Required Skills:

  • Bachelor’s degree in Science or a healthcare-related field.

  • 4+ years of experience in Pharmacovigilance.

  • Hands-on experience with ICSR processing and QC.

  • Experience with Argus, ArisG, or Veeva Safety databases.

  • Knowledge of MedDRA coding and FDA, ICH, and EU pharmacovigilance regulations.

  • Strong communication, analytical, and documentation skills.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 10128873
  • Position Id: 9115188
  • Posted 5 hours ago
Contact the job poster
SM

Sharanya M Salian

Recruiter @ SSI People

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