Pharmacovigilance Associate @ Clariwellglobal

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Pharmacovigilance Associate

Clariwellglobal
6 Positions
Bengaluru
2 months ago
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Job Description

Perform case intake, triage, and processing of Individual Case Safety Reports (ICSRs).
Review and validate adverse event reports from healthcare professionals, patients, and literature.
Enter and maintain accurate data in the safety database (e.g., Argus, ArisG, or equivalent).
Assess seriousness, expectedness, and causality of reported events.
Code adverse events and drugs using MedDRA and WHO-DD dictionaries.
Prepare and submit safety reports to regulatory authorities within compliance timelines.
Support aggregate safety reporting (PBRERs, PSURs) and signal detection activities.
Participate in quality checks, audits, and inspections as required.
Collaborate with cross-functional teams to ensure timely exchange of safety data.
Maintain awareness of current pharmacovigilance regulations and industry best practices.

Employement Category:

Employement Type: Full time
Industry: Pharma / Biotech
Role Category: Nursing
Functional Area: Not Specified
Role/Responsibilies: Pharmacovigilance Associate

Contact Details:

Company: Clariwellglobal
Location(s): Bengaluru

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Keyskills: healthcare clinical trials pharmacovigilance pharmacy pharma medical coding clinical research

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Designation / Expected Role

Current / Recent Company (*)

Experience (*)

Expected Salary (*)

Desired Industry (*):

Functional area / Department (*):

Enter Skills (key skills, subjects, technologies & roles to use in search)

Write briefly about yourself, your experience and education (*)

Attach ResumeMax 2.38 MB (RTF, PDF, DOC, DOCX formats only parsed)

Please, check the file size and type.

Add social media [ + ]

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I agree with website service terms and conditions

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Pharmacovigilance Associate @ Clariwellglobal

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