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Pharmacovigilance Associate

0-2 years
Not Disclosed
10 Oct. 27, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Pharmacovigilance Associate

Employer: ICON Strategic Solutions
Location: Mexico (CDMX, Remote / Homeworking)
Salary: Competitive
Start Date: 21 October 2025
Closing Date: 20 November 2025
Contract Type: Full-Time, Permanent
Experience Level: Entry to Intermediate


About the Company

ICON plc is a world-leading healthcare intelligence and clinical research organization. ICON fosters an inclusive environment that drives innovation and excellence, uniting professionals to shape the future of clinical development worldwide.


Role Overview

The Pharmacovigilance Associate will play a crucial role in monitoring and ensuring the safety of pharmaceutical products. This position involves collecting, analyzing, and reporting adverse events while supporting global compliance and patient safety initiatives.


Key Responsibilities

  • Collect and review adverse event (AE) reports to ensure timely and accurate submissions in line with regulatory guidelines.

  • Conduct signal detection and risk assessment activities to identify potential safety concerns.

  • Collaborate with cross-functional teams to resolve safety-related inquiries and investigations.

  • Stay up-to-date with pharmacovigilance regulations, company policies, and industry best practices.

  • Assist in preparing safety reports, aggregate reports, and regulatory submissions.


Candidate Profile

  • Education: Bachelor’s degree in life sciences, pharmacy, or a related field (advanced degree preferred).

  • Experience: Prior exposure to pharmacovigilance, drug safety, or clinical research preferred.

  • Strong analytical and data accuracy skills with excellent attention to detail.

  • Excellent communication and interpersonal skills to ensure effective collaboration.

  • Commitment to maintaining compliance and high standards of data integrity and patient safety.


What ICON Offers

ICON believes that its success depends on the quality and diversity of its people.
Employees enjoy a supportive, performance-driven environment with global career opportunities and a strong focus on well-being and work-life balance.

Benefits include:

  • Competitive annual leave entitlements.

  • Comprehensive health insurance plans for employees and their families.

  • Attractive retirement savings and pension options.

  • Global Employee Assistance Programme (LifeWorks) – 24/7 access to professional wellness support.

  • Life assurance and flexible optional benefits such as:

    • Childcare vouchers

    • Gym membership discounts

    • Bike purchase schemes

    • Subsidized travel passes

    • Health assessments


Diversity & Inclusion

ICON is committed to an inclusive, discrimination-free workplace.
All qualified applicants will receive equal consideration regardless of race, gender, religion, sexual orientation, or disability status.


Accommodation Support

If you require a reasonable accommodation due to a medical condition or disability during the application process or while performing job functions, please submit a request through ICON’s accommodation portal.


How to Apply

Interested candidates are encouraged to apply directly, even if not meeting every requirement — ICON values potential and diverse experience.

  • Current ICON employees should apply via the internal careers portal.

  • Visit ICON Careers for more opportunities and benefit details.