01Key Responsibilities
- Monitor and report adverse drug reactions (ADRs) or events through established reporting channels.
- Assist in the processing of individual case safety reports (ICSRs) including data entry, quality review, and regulatory submission.
- Support in the preparation and submission of pharmacovigilance reports to regulatory authorities.
- Maintain up-to-date knowledge of regulations, guidelines, and company policies concerning pharmacovigilance.
- Ensure the accurate and timely recording of adverse events in safety databases.
- Participate in safety reviews, case assessments, and team discussions for risk minimization.
- Contribute to signal detection and risk management activities by performing literature reviews and case studies.
Qualifications & Skills:
- Bachelors degree in Life Sciences, Pharmacy, or a related field (e.g., BSc, MSc, BPharm, MPharm).
- Basic knowledge of pharmacovigilance principles and adverse drug reaction reporting.
- Good communication skills, both written and verbal.
Job Types: Full-time, Permanent, Fresher
Compensation: 15,245.01 - 45,233.53 per month
Perks:
- Health insurance
Schedule:
- Day shift
- Fixed shift
- Morning shift
Supplemental Compensation:
- Performance bonus
- Yearly bonus
Experience:
- total work: 1 year (preferred)
Work Location: In person .
