Drug Safety Trainee
About the Role
Roles & Responsibilities:
• Assist in processing Individual Case Safety Reports (ICSRs)
• Perform adverse event (AE) and serious adverse event (SAE) case intake
• Support case triage, data entry, and quality checks
• Ensure compliance with global pharmacovigilance regulations
• Work with medical terminologies such as MedDRA and WHO-DD
• Maintain accurate drug safety documentation
• Collaborate with senior drug safety associates and PV teams
Qualification:
• M.Pharm / B.Pharm / PharmD / MSc Life Sciences
Experience:
• Freshers only
No. of Openings: 30
Skills:
• Basic understanding of Pharmacovigilance and drug safety processes
• Awareness of adverse events and clinical pharmacology
• Familiarity with medical terminology
• Good attention to detail and willingness to learn
About the Organization:
The company is a global pharmaceutical organization with established pharmacovigilance operations, offering freshers hands-on exposure and a strong foundation in drug safety and clinical safety operations.
Interested and eligible candidates should share their updated CV to email: sahana.s@randstad.in
AI Career Power Suite
Resume Analyst
Unlock refined AI insights.
Interested?
Frequently Asked Questions
Everything you need to know about the process