Pharmacovigilance Associate
About the Role
Role & Responsibilities
• Perform end-to-end pharmacovigilance case processing for clinical trial safety cases
• Collect, assess, process, and submit adverse event (AE) and serious adverse event (SAE) reports
• Ensure timely and accurate data entry in LSMV (LifeSphere MultiVigilance) database
• Maintain compliance with global pharmacovigilance regulations (ICH-GCP, GVP, FDA, EMA)
• Support signal detection activities and risk management assessments
• Collaborate with cross-functional teams on safety queries and investigations
• Stay updated with the latest drug safety guidelines and industry standards
Qualification
• Bachelor’s degree in Life Sciences, Pharmacy, or a related discipline
Experience
• Minimum 2+ years of experience in pharmacovigilance case processing
• Hands-on experience in Clinical Trial Safety Cases or LSMV/Argus/Safety Databases
Skills
• Strong analytical skills with high attention to detail
• Excellent written and verbal communication skills
• Proven commitment to quality, compliance, and patient safety
About the Company
• ICON plc is a global leader in healthcare intelligence and clinical research, specializing in providing comprehensive clinical development and outsourcing solutions to the pharmaceutical, biotechnology, and medical device industries.
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