Collect, review, and process adverse event reports from clinical trials and post-marketing sources.
Perform data entry of case details into safety databases accurately and within timelines.
Assist in coding adverse events, medical history, and medications using MedDRA and WHO-DD.
Support literature screening for identification of safety signals.
Ensure compliance with company SOPs, regulatory requirements, and global pharmacovigilance standards.
Communicate effectively with internal teams (medical writers, safety scientists, quality assurance).
Maintain confidentiality and accuracy in safety data documentation.
Participate in training programs to stay updated with current PV practices and regulations.
Job Types: Full-time, Permanent, Fresher
Pay: ₹361,948.28 - ₹681,494.02 per year
Benefits:
Paid sick time
Paid time off
Provident Fund
Work from home
Work Location: In person
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