ICON plc hiring Pharmacovigilance Associate Chennai 2026. Check eligibility, skills, responsibilities and apply for PV case processing pharma job opportunity today.
Introduction
If you are experienced in drug safety and looking to advance your career in pharmacovigilance, this is a strong opportunity. The Pharmacovigilance Associate at ICON plc focuses on post-marketing case processing and global safety reporting. This role is ideal for professionals with hands-on PV experience who want to work in a leading CRO and contribute to patient safety.
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, Nursing, BAMS, BHMS |
| Salary | As per company standards |
Company Overview
ICON plc is a world-renowned clinical research organization providing healthcare intelligence and development services. The company supports pharmaceutical, biotechnology, and medical device industries with innovative solutions. ICON is known for its inclusive work culture, global presence, and commitment to improving patient outcomes through high-quality research and safety monitoring.
Job Location & Employment Type
- Location: Chennai, India
- Work Mode: Office with flexible work options
- Employment Type: Full-Time
Open Positions / Department Details
- Department: Pharmacovigilance (Post-Marketing Surveillance)
- Role Level: Associate
- Focus Area: Case processing, safety reporting, regulatory compliance
Key Roles & Responsibilities
As a Pharmacovigilance Associate at ICON plc, you will:
- Process Individual Case Safety Reports (ICSRs) from post-marketing sources
- Collect, assess, and validate adverse event data for regulatory submission
- Perform case triage, data entry, and narrative writing
- Code medical events, drugs, and histories using MedDRA and WHO-DD
- Conduct quality checks and ensure compliance with global PV standards
- Apply seriousness, expectedness, and causality assessments
- Manage safety inbox and acknowledge case receipts
- Generate queries and follow-ups for incomplete data
- Support aggregate reporting activities such as PSUR and DSUR
- Handle literature case processing and reconciliation activities
- Maintain compliance with SOPs, SDEA, KPI, and SLA requirements
- Collaborate with cross-functional teams for safety-related investigations
- Mentor junior team members and support training initiatives
Eligibility Criteria
Education
- Degree in:
- B.Pharm / M.Pharm / Pharm.D
- BSc / MSc Nursing
- BDS, BAMS, BHMS
Experience
- Minimum 2 years of experience in pharmacovigilance
- Hands-on experience in post-marketing case processing (mandatory)
Skills Required
- Strong knowledge of pharmacovigilance and safety reporting
- Experience in ICSR processing and regulatory compliance
- Familiarity with MedDRA and WHO-DD coding
- Understanding of PSUR, DSUR, and reconciliation processes
- Attention to detail and analytical skills
- Good communication and teamwork abilities
- Knowledge of global PV regulations and guidelines
Salary & Benefits
- Salary: As per company standards
- Health insurance and wellness programs
- Competitive retirement and financial benefits
- Employee assistance programs for mental health support
- Paid leaves and work-life balance initiatives
- Learning and development opportunities
- Inclusive and diverse work environment
Selection Process
The hiring process generally includes:
- Application screening
- Technical interview (PV case processing)
- Managerial round
- HR discussion
Candidates with strong case processing experience will be preferred.
How to Apply
Interested candidates can apply through the official ICON careers portal.
- Apply as soon as possible (no fixed deadline mentioned)
Important Dates
- Last Date: Not specified
Why Apply for This Job?
The Pharmacovigilance Associate at ICON plc is a great opportunity for professionals aiming to grow in drug safety and regulatory compliance. Here’s why:
- Work with a globally recognized CRO
- Gain expertise in post-marketing surveillance
- Exposure to international safety reporting standards
- Opportunity to grow into senior PV roles
- Strong focus on employee well-being and career development
FAQs
1. Who can apply for this job?
Candidates with pharmacy, nursing, or medical background and PV experience can apply.
2. Is experience mandatory?
Yes, at least 2 years of pharmacovigilance case processing experience is required.
3. What is the salary offered?
Salary is based on company standards and experience.
4. What skills are required?
ICSR processing, MedDRA coding, safety reporting, and regulatory knowledge are essential.
5. Is this a remote job?
No, this is an office-based role with flexible working options.
Conclusion
The Pharmacovigilance Associate at ICON plc offers a solid platform for professionals looking to advance in drug safety and regulatory compliance. With strong global exposure and career growth opportunities, this role is ideal for experienced PV professionals. Apply now to take your career forward.
Disclaimer
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