ICON Pharmacovigilance Specialist Jobs

ICON Hiring Pharmacovigilance Specialist – High-Paying Drug Safety Jobs in Chennai & Trivandrum

ICON plc is hiring experienced professionals for Pharmacovigilance Specialist roles in Chennai and Trivandrum with flexible remote or office work options. This is a full-time opportunity in the Pharmacovigilance & Patient Safety department for candidates with strong experience in drug safety, adverse event reporting, and regulatory compliance.

Multiple openings are expected for this role, targeting experienced professionals with 6+ years of experience in pharmacovigilance and clinical safety. If you are looking to move into a high-growth, high-paying clinical research career with a global CRO, this role offers strong long-term potential.

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Company Overview

ICON plc is a globally recognized clinical research organization (CRO) and healthcare intelligence provider. The company partners with leading pharmaceutical, biotechnology, and medical device organizations to accelerate drug development and improve patient outcomes.

With operations across more than 100 countries, ICON plays a critical role in clinical trials, regulatory consulting, and drug safety monitoring. The organization is known for its strong compliance framework, advanced data analytics, and commitment to patient-centric innovation.

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Job Role & Responsibilities

Pharmacovigilance Specialist (Drug Safety)

• Review, collect, and analyze adverse event reports to ensure compliance with global pharmacovigilance regulations
• Perform signal detection and risk assessment to identify potential safety concerns
• Prepare and submit safety reports to regulatory authorities within defined timelines
• Collaborate with clinical, regulatory, and medical teams for safety evaluations
• Support audits, inspections, and pharmacovigilance system compliance activities
• Stay updated with global drug safety regulations, including ICH guidelines and local requirements

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Eligibility / Qualifications

• Educational Qualification: B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry)
• Experience: Minimum 6+ years in pharmacovigilance or drug safety roles
• Strong knowledge of adverse event reporting, signal detection, and regulatory submissions
• Experience in clinical research or pharmaceutical industry preferred
• Excellent analytical, communication, and documentation skills

Relevant Courses: B.Pharm, M.Pharm, Pharm.D, BSc Life Sciences, MSc Biotechnology, MSc Microbiology, MSc Biochemistry

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Location & Salary

• Job Location: Chennai, Tamil Nadu & Trivandrum, Kerala
• Work Mode: Remote / Hybrid / Office
• Salary Range: ₹10 LPA – ₹22 LPA (approximate based on pharmacovigilance experience and CRO standards)

This salary reflects strong demand for experienced drug safety professionals in global clinical research organizations.

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Application Process

Apply directly through the official ICON careers portal:

Apply Here: https://careers.iconplc.com/job/pharmacovigilance-specialist-in-india-chennai-jid-50335

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Frequently Asked Questions (FAQs)

Is this role suitable for freshers?

No, this role requires a minimum of 6 years of pharmacovigilance experience.

What is pharmacovigilance?

Pharmacovigilance involves monitoring the safety of medicines by detecting, assessing, and preventing adverse effects.

What career growth can I expect?

You can grow into Senior Drug Safety Specialist, Pharmacovigilance Manager, or Global Safety Lead roles.

Is this a remote job?

Yes, this role offers flexible remote or hybrid working options.

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Summary

Category	Details
Company	ICON plc
Vacancies	Pharmacovigilance Specialist
Required Education	B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry)
Experience	6+ years in pharmacovigilance / drug safety