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Drug Safety Associate

0 years

2 - 9 Lacs

Satara, Maharashtra

Posted:2 weeks ago| Platform:

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Skills Required

Laboratory experience Machine learning Quality control Data entry In-person

Work Mode

On-site

Job Type

Full Time

Job Description

Responsibilities: Collect and process adverse event reports from clinical trials and post-marketing sources Perform case triage, data entry, and quality checks in safety databases Assist in preparation of regulatory reports (e.g., CIOMS, MedWatch) Conduct literature screening for safety data Ensure compliance with global pharmacovigilance regulations and SOPs Job Types: Full-time, Fresher Pay: ₹286,000.00 - ₹970,000.00 per year Benefits: Health insurance Schedule: Day shift Work Location: In person

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