Apply for Pharmacovigilance Associate job at ICON plc 2026. Check eligibility, post marketing experience, and case processing role details online now.
Introduction
The field of pharmacovigilance plays a critical role in ensuring drug safety and protecting patient health worldwide. The Pharmacovigilance Associate Job at ICON plc offers a strong opportunity for professionals with experience in case processing and post-marketing surveillance.
This role is ideal for candidates who want to advance their careers in drug safety, adverse event reporting, and global regulatory compliance within a leading clinical research organization.
Job Overview
| Particulars | Details |
|---|---|
| Job Title | Pharmacovigilance Associate |
| Company Name | ICON plc |
| Location | Chennai, India |
| Employment Type | Full-Time (Office with Flex) |
| Department | Pharmacovigilance / Drug Safety |
| Experience Required | Minimum 2 Years |
| Education | B.Pharm, M.Pharm, Pharm.D, BDS, BSc Nursing, MSc Nursing, BAMS, BHMS |
| Salary | As per company norms |
Company Overview
ICON plc is a globally recognized healthcare intelligence and clinical research organization that provides outsourced services to pharmaceutical, biotechnology, and medical device companies.
ICON focuses on delivering high-quality clinical development solutions while maintaining strong regulatory compliance and patient safety standards.
Job Location & Employment Type
This position is based in Chennai, India, with an “Office with Flex” model allowing some flexibility in working arrangements.
Open Positions / Department Details
The role is part of the Pharmacovigilance (PV) team, responsible for post-marketing safety case processing and ensuring compliance with global safety regulations.
Key Roles & Responsibilities
- Collect, review, and process adverse event (AE) reports in compliance with regulatory timelines
- Perform case triage and book-in activities in safety databases
- Accurately enter case data and prepare detailed narratives
- Code medical terms, drugs, and history using MedDRA and WHO-DD
- Apply product labeling and perform quality control (QC) checks
- Handle safety inbox and acknowledge receipt of cases
- Generate queries and follow up for missing or incomplete data
- Assess seriousness, causality, and expectedness of adverse events
- Support reconciliation and aggregate reporting (PSUR/DSUR)
- Process literature-based Individual Case Safety Reports (ICSRs)
- Maintain compliance with SOPs, SDEA, KPI, and SLA requirements
- Mentor new team members and contribute to SOP reviews
- Collaborate with cross-functional teams for safety investigations
Eligibility Criteria
Education
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Nursing, or related fields
- Accepted qualifications include B.Pharm, M.Pharm, Pharm.D, BDS, BSc Nursing, MSc Nursing, BAMS, BHMS
Experience
- Minimum 2 years of experience in pharmacovigilance
- Mandatory experience in post-marketing case processing
Skills Required
- Strong knowledge of pharmacovigilance processes and regulations
- Hands-on experience in ICSR case processing
- Familiarity with MedDRA and WHO-DD coding
- Understanding of global safety reporting requirements
- Strong analytical and data interpretation skills
- Attention to detail and accuracy in documentation
- Good communication and teamwork skills
Salary & Benefits
- Salary: As per company norms
- Competitive compensation package
- Health insurance benefits for employees and families
- Retirement and financial planning options
- Flexible work model supporting work-life balance
- Employee Assistance Program (24/7 support)
- Life insurance coverage
- Additional benefits such as gym memberships, childcare support, and travel benefits
Selection Process
The recruitment process generally includes:
- Resume screening
- Technical interview (Pharmacovigilance & case processing)
- HR discussion
- Final selection
How to Apply
Candidates can apply through the official online application portal. Ensure your resume highlights your pharmacovigilance experience, especially in post-marketing case processing.
Important Dates
- Last Date to Apply: Not specified (Apply early recommended)
Why Apply for This Job?
The Pharmacovigilance Associate Job at ICON plc is a valuable opportunity for professionals aiming to grow in drug safety and global pharmacovigilance operations.
Key benefits include:
- Work with a globally recognized CRO
- Gain expertise in post-marketing surveillance
- Exposure to international safety reporting standards
- Opportunity to mentor and grow within the organization
- Strong career progression in pharmacovigilance
This role is particularly suitable for candidates looking to advance in drug safety, regulatory affairs, or clinical research domains.
FAQs
1. What is the eligibility for Pharmacovigilance Associate Job at ICON plc?
Candidates must have relevant life sciences or pharmacy qualifications with at least 2 years of PV case processing experience.
2. Is post-marketing experience mandatory?
Yes, experience in post-marketing surveillance case processing is required.
3. What coding systems are used in this role?
MedDRA and WHO-DD coding systems are used for case processing.
4. What is the job location?
The job is based in Chennai with flexible working options.
5. Is this job suitable for freshers?
No, this role requires prior pharmacovigilance experience.
Conclusion
The Pharmacovigilance Associate Job at ICON plc 2026 offers an excellent platform for experienced professionals to strengthen their expertise in drug safety and global regulatory compliance. With strong benefits, career growth opportunities, and global exposure, this role is ideal for advancing in pharmacovigilance.
Interested candidates should apply as soon as possible to secure this opportunity.
Disclaimer
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