Instagram
youtube
Facebook

Pharmacovigilance Associate

2 years
Not Disclosed
10 Dec. 5, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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.