Position: Pharmacovigilance (PV) Associate / Sr. PV Associate
Key Responsibilities:
- Review and process safety data (pre/post-marketing, drugs & medical devices) in line with project guidelines.
- Analyze scientific abstracts and literature for safety insights.
- Generate and maintain accurate data listings from safety databases.
- Conduct adverse event (AE) follow-ups via phone/email.
- Assist in creating Safety Management Plans and reports (PSMF, RMP, PBRER).
- Collaborate with QPPV and cross-functional teams on safety issues.
- Contribute to DSURs, IND Annual Reports, PSURs, and other safety documents.
- Perform SAE/AE reconciliation and ensure data quality.
- Participate in signal detection and risk management activities.
- Support regulatory audits and compliance efforts.
Qualifications & Skills:
- Education: Bachelor’s or Master’s in Life Sciences, Pharmacy, Medicine, or Dentistry.
- Experience: 1–6 years in pharmacovigilance, clinical research, or drug safety.
- Technical Proficiency: Safety databases, literature screening, regulatory reporting.
- Soft Skills: Attention to detail, time management, and clear communication.
- Regulatory Knowledge: ICH-GCP, FDA, EMA guidelines preferred.
Why Join ICON?
ICON offers more than just a job—it offers a career path in a purpose-driven organization.
✅ Health Insurance – Extensive medical coverage for you and your family.
✅ Retirement Plans – Helping you plan for a secure future.
✅ Work-Life Balance – Flexible policies and wellness initiatives.
✅ Global Support – 24/7 mental health and wellbeing resources via LifeWorks.
✅ Perks & Discounts – Childcare support, gym memberships, travel subsidies, and more.
🔗 How to Apply:
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Ready to shape the future of drug safety? Apply today and become a part of a team that’s changing lives through science.
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