ICON plc is a global leader in healthcare intelligence and clinical research, dedicated to advancing medical innovation and improving patient outcomes. With a strong commitment to excellence, diversity, and inclusion, ICON fosters a dynamic work environment where professionals can thrive while contributing to the future of clinical development.
Job Description: Pharmacovigilance Associate
Key Responsibilities:
- Collect, review, and assess adverse event (AE) reports to ensure compliance with regulatory guidelines.
- Perform signal detection and risk assessment to identify potential drug safety concerns.
- Collaborate with cross-functional teams to address safety-related inquiries and investigations.
- Maintain up-to-date knowledge of pharmacovigilance regulations (GVP, ICH, FDA, EMA).
- Assist in preparing safety reports, PSURs, DSURs, and regulatory submissions.
- Ensure timely and accurate documentation of pharmacovigilance data.
Qualifications & Skills:
- Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field (Master’s preferred).
- Prior experience in pharmacovigilance, drug safety, or clinical research is advantageous.
- Strong analytical skills with attention to detail in data interpretation.
- Excellent communication and teamwork abilities.
- Familiarity with safety databases (Argus, ARISg, VigiFlow) is a plus.
Why Join ICON plc?
ICON offers a competitive salary and comprehensive benefits, including:
✅ Health insurance for you and your family
✅ Retirement savings plans
✅ Global Employee Assistance Program (EAP)
✅ Flexible leave policies
✅ Wellness programs (gym discounts, health assessments, etc.)
ICON is an equal-opportunity employer, committed to fostering an inclusive workplace free from discrimination.
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