ICON PLC Hiring Senior Pharmacovigilance Associate

ICON Hiring Senior Pharmacovigilance Associate in Chennai | Drug Safety and PV Jobs

ICON plc has announced recruitment for the position of Senior Pharmacovigilance Associate in Chennai. This opportunity is ideal for experienced pharmacovigilance and drug safety professionals from pharmacy, nursing, dental, ayurveda, and healthcare backgrounds who are looking to advance their careers in post-marketing surveillance, adverse event reporting, clinical trial safety operations, and global pharmacovigilance.

Candidates with 4+ years of experience in pharmacovigilance case processing, ICSR handling, post-marketing surveillance, aggregate reporting, and global safety operations are encouraged to apply for this hybrid opportunity.

The company is looking for professionals with expertise in drug safety operations, adverse event processing, safety database management, healthcare compliance, regulatory reporting, and pharmacovigilance quality systems.

This role provides excellent exposure to global clinical safety operations, healthcare analytics, regulatory affairs, aggregate reporting, signal detection, and pharmaceutical compliance systems.

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About ICON plc

ICON plc is a globally recognized healthcare intelligence and clinical research organization specializing in clinical development, pharmacovigilance, healthcare analytics, regulatory support, and pharmaceutical research services.

The company supports pharmaceutical organizations, biotechnology firms, medical device companies, and healthcare institutions through advanced clinical research and drug safety solutions.

ICON is known for its expertise in pharmacovigilance operations, clinical trials, healthcare technology systems, regulatory affairs, and healthcare compliance services.

Working at ICON provides professionals exposure to international clinical research programs, global healthcare systems, advanced pharmacovigilance operations, and pharmaceutical innovation.

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Senior Pharmacovigilance Associate Vacancy Details

Position

Senior Pharmacovigilance Associate

Department

Drug Safety & Pharmacovigilance

Employment Type

Full-Time

Work Model

Hybrid

Job ID

JR139662

Location

Chennai

Experience Required

4+ Years

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Job Role and Responsibilities

Selected candidates will support global pharmacovigilance operations, adverse event processing, drug safety compliance, and healthcare reporting activities.

Key Responsibilities

• Process and manage Individual Case Safety Reports (ICSRs)
• Handle post-marketing surveillance and adverse event reporting activities
• Analyze safety data and identify potential safety signals
• Prepare aggregate reports including PSUR and DSUR
• Support seriousness, causality, and expectedness assessments
• Maintain pharmacovigilance databases and healthcare documentation
• Process literature ICSRs and ensure compliance standards
• Support reconciliation processes and safety monitoring activities
• Collaborate with clinical teams, medical reviewers, and healthcare stakeholders
• Participate in audits and regulatory inspections
• Mentor junior pharmacovigilance associates and support training activities
• Maintain compliance with GCP, GVP, ICH, and healthcare regulations
• Monitor KPI and SLA adherence for pharmacovigilance operations

Candidates with expertise in healthcare analytics, regulatory affairs, clinical research operations, aggregate reporting, signal detection, medical review, and healthcare compliance systems may have an added advantage.

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Eligibility and Qualifications

Candidates applying for this Senior Pharmacovigilance Associate role should possess strong drug safety and healthcare documentation expertise.

Required Qualification

B.Pharm, M.Pharm, PharmD, BDS, BSc Nursing, MSc Nursing, BAMS, BHMS

Required Experience

Minimum 4+ years of pharmacovigilance case processing experience in post-marketing surveillance.

Required Skills

• Expertise in ICSR processing and adverse event reporting
• Strong knowledge of pharmacovigilance regulations and healthcare compliance
• Understanding of PSUR, DSUR, and aggregate reporting
• Knowledge of seriousness, causality, and expectedness assessments
• Experience with safety databases and pharmacovigilance systems
• Good analytical and critical thinking abilities
• Excellent communication and documentation skills
• Ability to mentor and train junior team members
• Strong understanding of GCP, GVP, and ICH guidelines

Professionals with experience in clinical trial safety, healthcare analytics, regulatory affairs, signal detection, and global drug safety operations are encouraged to apply.

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Location and Salary

Location

Chennai

Salary

The estimated salary for Senior Pharmacovigilance Associate roles generally ranges between ₹8 LPA and ₹16 LPA depending on post-marketing surveillance experience, aggregate reporting expertise, and global pharmacovigilance exposure.

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Why Pharmacovigilance Careers Are Growing

Pharmacovigilance and drug safety professionals play a major role in ensuring patient safety, regulatory compliance, adverse event monitoring, and pharmaceutical risk management.

As pharmaceutical companies continue expanding global clinical trials and post-marketing safety programs, the demand for experienced pharmacovigilance professionals is increasing rapidly.

Professionals in this field can build long-term careers in:

• Pharmacovigilance
• Drug Safety Operations
• Regulatory Affairs
• Clinical Research
• Aggregate Reporting
• Signal Detection
• Medical Review
• Healthcare Analytics
• Pharmaceutical Compliance

This opportunity at ICON provides candidates exposure to international healthcare systems, advanced pharmacovigilance technologies, regulatory environments, and global pharmaceutical operations.

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How to Apply

Interested candidates can apply through the official ICON careers portal using the application link below:

https://careers.iconplc.com/job/senior-pharmacovigilance-associate-in-india-chennai-jid-46821

Candidates should ensure all educational details, pharmacovigilance experience, and professional information are updated before submitting the application.

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Frequently Asked Questions

What experience is required for this ICON role?

Candidates must have at least 4+ years of pharmacovigilance case processing experience in post-marketing surveillance.

What qualifications are eligible?

Candidates with B.Pharm, M.Pharm, PharmD, Nursing, BAMS, BHMS, and BDS qualifications can apply.

What is the work model for this role?

The role follows a hybrid work model.

What is the salary range for this role?

The estimated salary range is ₹8 LPA to ₹16 LPA depending on pharmacovigilance expertise and experience.

Which departments can candidates grow into after this role?

Candidates can build careers in Drug Safety, Regulatory Affairs, Signal Detection, Aggregate Reporting, and Clinical Safety Operations.

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ICON Senior Pharmacovigilance Associate Recruitment Overview

Company	ICON plc
Department Vacancies	Senior Pharmacovigilance Associate
Qualification	B.Pharm, M.Pharm, PharmD, BDS, Nursing, BHMS
Experience	4+ Years
Location	Chennai