Job Description
- Collect, review, and process adverse event (AE) and adverse drug reaction (ADR) reports.
- Enter safety data into pharmacovigilance databases accurately.
- Assess case information for completeness and follow up for missing details when required.
- Perform medical coding using standards such as MedDRA and WHO Drug Dictionary (after training).
- Ensure compliance with regulatory guidelines and company standard operating procedures (SOPs).
- Support the preparation and submission of safety reports to regulatory authorities.
- Maintain confidentiality and accurate documentation of safety data.
- Collaborate with quality assurance and global safety teams.
Skills Required
- Bachelor's or Master's degree in Pharmacy, Life Sciences, Nursing, or related fields.
- Basic understanding of pharmacology and drug safety.
- Good communication and documentation skills.
- Attention to detail and analytical thinking.
- Basic computer skills (MS Office) and willingness to learn safety databases.
Pay: ₹275,000.00 - ₹450,000.00 per year
Benefits:
- Paid sick time
- Provident Fund
Work Location: In person
