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Pharmacovigilance Associate

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ICON
Freshers years
Not Disclosed
Bangalore, Chennai, Remote, India, India
10 May 7, 2026
Job Description
Job Type: Full Time Hybrid Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title

Pharmacovigilance Associate
Employment Type: Full-Time
Work Mode: Office or Home (Remote flexibility)
Locations: Chennai, Bangalore, India


About the Company – ICON plc

ICON plc is a world-leading clinical research and healthcare intelligence organization.

  • Specializes in clinical development and drug research

  • Focuses on innovation, patient safety, and regulatory excellence

  • Promotes an inclusive and high-performance culture

  • Committed to diversity, equality, and belonging in the workplace


Role Overview

The Pharmacovigilance Associate plays a key role in ensuring drug safety and patient protection by monitoring, analyzing, and reporting adverse events related to pharmaceutical products.

You will contribute to maintaining regulatory compliance and supporting global pharmacovigilance operations.


Key Responsibilities

1. Adverse Event Reporting

  • Collect and review adverse event (AE) reports

  • Ensure accurate, complete, and timely safety reporting

  • Follow global pharmacovigilance regulatory guidelines


2. Safety Monitoring & Signal Detection

  • Conduct signal detection activities

  • Perform risk assessment to identify potential safety issues

  • Support evaluation of drug safety profiles


3. Cross-Functional Collaboration

  • Work with internal and cross-functional teams

  • Support safety-related investigations and inquiries

  • Coordinate with stakeholders for pharmacovigilance activities


4. Regulatory Compliance

  • Maintain up-to-date knowledge of:

    • Pharmacovigilance regulations

    • Industry best practices

  • Support preparation of:

    • Safety reports

    • Regulatory submissions


5. Documentation & Reporting

  • Assist in preparing safety documentation

  • Ensure compliance with quality standards and regulatory requirements

  • Maintain accurate pharmacovigilance records


Candidate Profile

Education

  • Bachelor’s degree in Life Sciences, Pharmacy, or related field

  • Advanced degree preferred

Experience

  • Experience in pharmacovigilance or drug safety preferred

  • Exposure to clinical or pharmaceutical environments is an advantage


Skills Required

  • Strong analytical and data interpretation skills

  • High attention to detail

  • Strong written and verbal communication skills

  • Ability to collaborate effectively with teams and stakeholders

  • Commitment to quality and regulatory compliance


Work Culture & Benefits

ICON offers a supportive and inclusive work environment focused on well-being and professional growth.

Benefits Include:

  • Competitive salary

  • Annual leave benefits

  • Health insurance options for employees and families

  • Retirement planning support

  • Employee Assistance Programme (24/7 global support)

  • Life assurance

  • Flexible benefits (varies by country), such as:

    • Childcare vouchers

    • Gym membership discounts

    • Travel passes

    • Health assessments


Equal Opportunity Statement

ICON is committed to:

  • Equal employment opportunities

  • A workplace free from discrimination and harassment

  • Inclusive hiring practices

All qualified applicants are considered regardless of:

  • Race

  • Gender identity

  • Religion

  • Disability

  • National origin

  • Sexual orientation

  • Veteran status


Additional Information

  • Candidates are encouraged to apply even if they do not meet all requirements

  • Accommodation is available for applicants with medical conditions or disabilities

  • Current ICON employees can apply through internal portals