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Drug Safety Specialist I / II

1 - 6 years

Hyderabad Gurugram

Posted:17 hours ago

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Job Description

  • Perform end-to-end ICSR case processing (Spontaneous / Clinical Trial / Literature cases)
  • Execute accurate data entry activities as part of core responsibilities (initial phase)
  • Handle case workflows including triage, data entry, coding, narrative writing, and submission readiness
  • Ensure compliance with global pharmacovigilance guidelines, SOPs, and regulatory requirements
  • Perform quality checks (QC) on processed cases based on experience and performance.

Skills Required

Drug Safety Literature cases Clinical Trial narrative writing ICSR Case processing pharmacovigilance Processing Case

Work Mode

Work from Office

Job Type

Full Time

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