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Pharmacovigilance Associate

ICON
0-2 years
Not Disclosed
Ciudad de México, Mexico, New Mexico, Mexico
10 May 26, 2026
Job Description
Job Type: Full Time 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

Location

Mexico (Homeworking / Remote – CDMX base)

Employment Type

Not specified (Typically full-time)

Company

ICON plc (ICON Strategic Solutions)


Role Overview

The Pharmacovigilance Associate at ICON plc is responsible for monitoring, evaluating, and reporting drug safety information, ensuring compliance with global pharmacovigilance regulations and supporting patient safety across clinical and post-marketing environments.


Key Responsibilities

1. Adverse Event Collection & Reporting

  • Collect and review adverse event (AE) reports

  • Ensure accurate, complete, and timely safety reporting

  • Support preparation of safety reports and regulatory submissions

  • Maintain compliance with global PV reporting guidelines


2. Safety Evaluation & Risk Assessment

  • Conduct signal detection activities

  • Perform safety and risk assessments

  • Identify potential safety concerns in products

  • Support ongoing pharmacovigilance surveillance activities


3. Cross-Functional Collaboration

  • Work with clinical, regulatory, and safety teams

  • Support safety-related queries and investigations

  • Communicate findings across stakeholders


4. Regulatory Compliance

  • Maintain up-to-date knowledge of PV regulations

  • Ensure compliance with industry best practices and guidelines

  • Support regulatory inspection readiness


Required Qualifications

Education

  • Bachelor’s degree in:

    • Life Sciences

    • Pharmacy

    • Or related field

  • Advanced degree preferred


Experience

  • Experience in pharmacovigilance, drug safety, or clinical/pharmaceutical environment preferred


Key Skills Required

Technical Skills

  • Understanding of pharmacovigilance systems and adverse event reporting

  • Knowledge of regulatory guidelines and compliance requirements

  • Data review and safety assessment skills

  • Experience with safety documentation and reporting tools


Analytical Skills

  • Strong attention to detail

  • Ability to analyze safety data accurately

  • Risk identification and evaluation capability


Soft Skills

  • Strong communication and interpersonal skills

  • Ability to work in cross-functional global teams

  • High level of accountability and quality focus

  • Commitment to compliance and ethical standards


Core Function

This role ensures global drug safety monitoring by collecting, analyzing, and reporting adverse events, contributing directly to patient safety and regulatory compliance in clinical and post-marketing settings.


About the Company

ICON plc is a global leader in clinical research and healthcare intelligence, supporting pharmaceutical development through clinical trials, pharmacovigilance, and regulatory services worldwide.