Pharmacovigilance Associate – Chennai
(Clinical Trial Case Processing / LSMV Database Expertise)**
Location: Chennai
Job ID: JR139660
Department: Drug Safety – ICON Full Service & Corporate Support
Employer: ICON plc
About the Company
ICON plc is a global leader in healthcare intelligence and clinical research, committed to driving innovation across drug development. With a strong focus on safety, quality, and regulatory excellence, ICON supports biopharma partners worldwide in accelerating clinical development while ensuring patient well-being.
Position Overview
ICON is seeking a Pharmacovigilance Associate with hands-on experience in clinical trial case processing or LSMV database operations. In this role, you will support end-to-end drug safety activities, ensuring the accurate collection, evaluation, and reporting of adverse events in compliance with global regulatory standards.
This opportunity is ideal for safety professionals looking to advance their careers in a fast-paced, high-standards clinical research environment.
Key Responsibilities
Perform accurate and timely case processing for adverse event reports in compliance with global regulatory requirements.
Manage Clinical Trial cases or utilize LSMV database skills for data entry and safety management.
Support signal detection, preliminary assessments, and safety risk evaluation.
Collaborate with cross-functional clinical and safety teams to resolve safety-related queries.
Maintain up-to-date expertise in pharmacovigilance regulations, ICH guidelines, and global safety reporting standards.
Experience Required
Minimum 2 years of pharmacovigilance case processing experience is mandatory.
Hands-on experience in Clinical Trial safety cases or LSMV database operations.
Strong understanding of regulatory requirements for safety reporting.
Ability to maintain high accuracy in data assessment and documentation.
Excellent communication skills and a proactive approach to teamwork.
Education Qualifications
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related field.
Advanced degrees (Master’s, PharmD) are considered an advantage.
What ICON Offers
ICON provides a supportive, performance-driven work environment with opportunities for growth in global drug safety. Benefits may include:
Competitive salary and performance-based rewards
Comprehensive health insurance plans
Retirement and financial planning programs
Generous annual leave and work-life balance initiatives
Global Employee Assistance Program (LifeWorks)
Flexible additional benefits such as childcare vouchers, gym memberships, travel subsidies, and more
Inclusive culture that promotes diversity, belonging, and equal opportunity
Why Join ICON?
Joining ICON means contributing to high-impact clinical programs that shape the future of global healthcare. The organization values integrity, collaboration, and excellence—offering a career path that supports continuous learning and professional development.
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