ICON plc Hiring Fresher for Pharmacovigilance Assistant I: PV Jobs 2026

ICON plc, a global leader in clinical research and healthcare intelligence, is hiring for the role of Pharmacovigilance Assistant I in Bangalore, India. This position is well‑suited for B.Pharm, M.Pharm, and Life Sciences graduates who want to start a career in pharmacovigilance, drug safety, and clinical research operations.

The role focuses on supporting safety data collection, adverse event reporting, and regulatory compliance activities. You will collaborate with cross‑functional teams to ensure accurate and timely safety reporting for both clinical trials and marketed products.

This is a strong entry‑level opportunity for professionals looking to step into the global pharmacovigilance industry and build a foundation in clinical safety operations.

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Job Overview

• Position: Pharmacovigilance Assistant I
• Department: PV
• Location: Banglore, India
• Experience: 0 to 2 Years
• Qualification: B.Pharm, M.Pharm
• Job Type: Full-Time

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Key Responsibilities – Pharmacovigilance Assistant I

• Support the collection, review, and processing of adverse event reports for both clinical trials and marketed products.
• Ensure timely and accurate entry of safety information into designated pharmacovigilance databases.
• Assist in preparing and submitting safety reports to regulatory authorities, sponsors, and other stakeholders as required.
• Work closely with cross‑functional teams to maintain regulatory compliance and ensure adherence to ICON’s safety procedures and protocols.
• Maintain detailed, organized records of all pharmacovigilance activities, ensuring documentation is complete, accurate, and audit‑ready.

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Required Skills & Qualifications

• Bachelor’s degree in Life Sciences, Pharmacy, or a closely related field.
• Pharmacovigilance Knowledge:Basic understanding of pharmacovigilance principles, safety reporting, and regulatory requirements is preferred.
• Strong ability to maintain accuracy in data review, documentation, and safety reporting, with a focus on high‑quality outputs.
• Effective written and verbal communication skills, with the ability to work collaboratively across cross‑functional teams.
• Ability to perform efficiently in a fast‑paced, regulated environment, ensuring adherence to safety guidelines, SOPs, and protocols.

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Why Join ICON?

• Join a leading global Contract Research Organization where you’ll gain exposure to international pharmacovigilance workflows, clinical operations, and safety processes.
• ICON provides structured learning, hands‑on training, and continuous development opportunities—ideal for building a long‑term career in drug safety and PV operations.
• Work closely with medical, clinical, and safety teams in a supportive environment that encourages teamwork, knowledge‑sharing, and professional growth.
• Grow into roles such as Drug Safety Associate, PV Specialist, Case Quality Reviewer, or other advanced pharmacovigilance positions within ICON’s global safety network.

How to Apply

Interested candidates should apply only through the official company career website using the link provided below.

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.

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