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Graduate Pharmacovigilance Associate
ICON plc
Chennai • Bangalore
0–1 Years
Pharmacovigilance
Drug Safety
Office with Flex
🏢 About ICON
ICON is a global clinical research organization (CRO) specializing in healthcare intelligence and drug development. The Graduate Pharmacovigilance Associate role offers exposure to global safety monitoring and regulatory reporting systems.
📌 Job Overview
- Role: Graduate Pharmacovigilance Associate
- Location: Chennai / Bangalore
- Work Model: Office with Flex
- Experience: Freshers / Entry-Level
- Qualification: B.Pharm / M.Pharm / Pharm.D / Life Sciences
🔬 Key Responsibilities
- Support collection & processing of AE/SAE cases
- Assist preparation of regulatory safety reports
- Ensure compliance with global pharmacovigilance guidelines
- Collaborate with cross-functional safety teams
- Maintain pharmacovigilance documentation & SOP adherence
- Participate in structured drug safety training programs
🎓 Eligibility & Skills
- Degree in Pharmacy or Life Sciences
- Strong documentation & analytical skills
- Basic understanding of pharmacovigilance concepts
- MS Office proficiency
- Good communication skills
📈 Career Growth Path
- Drug Safety Associate
- PV Scientist
- Safety Data Specialist
- Regulatory Affairs Professional
📌 Note Before You Apply:
Read the responsibilities carefully. Understanding AE/SAE processing and regulatory reporting will improve your chances of selection.
Read the responsibilities carefully. Understanding AE/SAE processing and regulatory reporting will improve your chances of selection.
🚀 Job Application Link
🛡️ Graduate Drug Safety & PV Entry Screening Guide:
ICON's pharmacovigilance tracking infrastructure filters graduate-level applications based on baseline analytical compliance indicators. Before submitting your candidature data structure through their main Workday portal node, refine your resume tracking keywords to reflect foundational academic or industrial awareness of Individual Case Safety Reports (ICSR), processing logs for serious adverse events (SAEs), initial triage workflows, basic MedDRA classification, and post-market safety tracking principles.
ICON's pharmacovigilance tracking infrastructure filters graduate-level applications based on baseline analytical compliance indicators. Before submitting your candidature data structure through their main Workday portal node, refine your resume tracking keywords to reflect foundational academic or industrial awareness of Individual Case Safety Reports (ICSR), processing logs for serious adverse events (SAEs), initial triage workflows, basic MedDRA classification, and post-market safety tracking principles.
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