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Job Description & How to Apply Below
Location:
Remote
Experience:
0–1 Year (Freshers Eligible)
Qualification:
Life Sciences / Pharmacy Graduates
Industry: Clinical Research / Pharmacovigilance
Job Summary:
We are looking for a detail-oriented and motivated Pharmacovigilance (PV) Associate – Fresher to support safety data management and pharmacovigilance activities. The role involves processing adverse event cases, ensuring regulatory compliance, and maintaining high standards of data accuracy and confidentiality.
Key Responsibilities:
Process Individual Case Safety Reports (ICSRs) from various sources
Perform data entry into safety databases (Argus / ArisG – basic level)
Conduct medical coding using MedDRA and WHO-Drug dictionaries
Review case data for accuracy, completeness, and consistency
Ensure compliance with GVP, ICH guidelines, and company SOPs
Maintain regulatory timelines for case processing
Follow up for missing or incomplete safety information
Assist in quality checks and internal audits
Maintain strict confidentiality and data integrity
Eligibility Criteria:
Educational
Qualification:
B.Pharm / M.Pharm / Pharm.
D
BSc / MSc – Life Sciences / Biotechnology / Microbiology / Nursing
Experience:
Freshers or candidates with 0–1 year experience
Basic understanding of pharmacovigilance concepts
Required Skills:
✔ Strong attention to detail
✔ Good written and verbal communication
✔ Basic knowledge of medical terminology
✔ Ability to work with SOPs and regulatory timelines
✔ MS Office proficiency (Word & Excel)
✔ Good typing accuracy
Position Requirements
Less than 1 Year
work experience
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