• Perform medical information contact center (MICC) activities and case intake
• Process adverse event (AE) and adverse drug reaction (ADR) reports
• Ensure timely, accurate, and compliant safety data entry
• Follow global pharmacovigilance regulations and internal SOPs
• Support safety surveillance and regulatory reporting activities
• Maintain proper documentation and quality standards
• B.Pharm / M.Pharm / BDS
• Freshers and experienced candidates can apply
• Basic knowledge of pharmacovigilance or clinical research
• Good communication and documentation skills
• Understanding of GCP, ICH guidelines, and drug safety concepts
• Willingness to learn and adapt in a regulated work environment
• Attention to detail and quality-oriented approach
Pharmazone is a growing organization in the pharmaceutical and clinical research domain, offering opportunities in clinical research and pharmacovigilance. The company provides structured learning, hands-on exposure, and clear career growth paths for freshers and experienced professionals in the life sciences industry.
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