Roles & Responsibilities:
• Review, assess, and process safety data in compliance with regulatory requirements.
• Perform pharmacovigilance activities including AE intake, triage, and case processing.
• Enter and manage safety cases in safety databases with accurate documentation.
• Perform MedDRA coding, product coding, and narrative writing.
• Handle literature case processing and follow-up activities.
• Ensure adherence to SOPs, internal guidelines, and quality standards.
• Meet defined productivity, quality, and turnaround time metrics.
• Attend project meetings and escalate issues to senior team members when required.
• Complete mandatory trainings within defined timelines.
Qualification:
• Bachelor’s degree in Pharmacy, Life Sciences, or a related healthcare discipline
• B. Pharm / M. Pharm (Preferred)
Experience:
• Freshers interested in Drug Safety / Pharmacovigilance
• Prior exposure or interest in Pharmacovigilance / Drug Safety will be an advantage
Skills:
• Good knowledge of medical terminology
• Strong written and verbal communication skills
• Working knowledge of MS Office and web-based applications
• High attention to detail and time management skills
• Ability to work independently and within a team
• Willingness to work in shifts
About the Organization:
IQVIA is a global leader in clinical research, pharmacovigilance, and healthcare intelligence, providing advanced analytics, technology solutions, and clinical services to the life sciences industry, and offering strong career growth opportunities for professionals entering the drug safety and regulatory domain.
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