Drug Safety / Pharmacovigilance Associate (Entry Level)

Roles & Responsibilities
• Assist in processing and reviewing Individual Case Safety Reports (ICSRs)
• Perform case intake, data entry, and quality review in safety databases
• Conduct adverse event (AE) and serious adverse event (SAE) assessments
• Support medical coding using MedDRA and WHO-DD
• Assist in case narratives, follow-ups, and reconciliation activities
• Ensure compliance with global regulatory timelines and SOPs
• Support safety reporting, audits, and inspection readiness
• Collaborate with cross-functional teams (Clinical, Regulatory, QA)

Qualification
• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Nursing, or related field

Experience
• 0–4 years of experience in pharmacovigilance or a related field

Skills
• Strong attention to detail and data accuracy
• Basic knowledge of safety databases and Microsoft Excel / MS Office
• Understanding of pharmacovigilance concepts and drug safety lifecycle
• Strong documentation and organizational skills
• Good written and verbal communication skills

About the Company
We are a global leader providing specialized services in Drug Safety and Pharmacovigilance. This entry-level role offers a fantastic opportunity to kickstart your career in a regulated clinical research environment while supporting critical pharmacovigilance activities for our USA-based client.