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Pharmacovigilance Associate

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ICON
0-2 years
Not Disclosed
10 Jan. 22, 2026
Job Description
Job Type: Full Time 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

Pharmacovigilance Associate | Remote (Mexico) | Full-Time

Company Overview:
ICON Strategic Solutions is a global leader in clinical research and healthcare intelligence, delivering innovative solutions across the pharmaceutical and life sciences industry. ICON fosters an inclusive, collaborative environment that encourages professional growth, innovation, and excellence in patient safety.

Role Overview – Pharmacovigilance Associate:
ICON is seeking a Pharmacovigilance Associate to join its dynamic, remote team in Mexico. The role is responsible for monitoring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information. The ideal candidate will have strong analytical skills, regulatory knowledge, and a commitment to patient safety.

Key Responsibilities:

  • Collect, review, and process adverse event reports in accordance with global and local regulatory guidelines.

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

  • Collaborate with cross-functional teams to support safety-related queries and investigations.

  • Maintain current knowledge of pharmacovigilance regulations and industry best practices.

  • Assist in the preparation of safety reports and regulatory submissions.

Qualifications & Experience:

  • Education: Bachelor’s degree in Life Sciences, Pharmacy, or a related field; advanced degrees preferred.

  • Experience: Prior experience in pharmacovigilance, drug safety, or clinical research is preferred.

  • Strong analytical and attention-to-detail skills in data collection and reporting.

  • Excellent written and verbal communication skills to effectively collaborate with stakeholders.

  • Commitment to high standards of compliance and quality in all pharmacovigilance activities.

Skills & Competencies:

  • Ability to work independently in a remote environment.

  • Collaborative mindset with strong interpersonal skills.

  • Proficiency in pharmacovigilance databases and regulatory tools is advantageous.

  • Adaptability to evolving processes and international regulatory requirements.

Location: Remote – Mexico (Homeworking)
Job Type: Full-Time
Start Date: 21 Jan 2026
Application Closing Date: 20 Feb 2026

Why Join ICON:

  • Be part of a global, innovative team shaping the future of clinical development.

  • Work in a diverse and inclusive culture that rewards high performance and nurtures talent.

  • Enjoy competitive compensation and benefits, including:

    • Annual leave entitlements

    • Health insurance for you and your family

    • Retirement planning and savings options

    • Life assurance and employee assistance programs

    • Flexible country-specific benefits such as childcare vouchers, gym memberships, or subsidized travel

  • Gain exposure to international pharmacovigilance operations and professional growth opportunities.

Equal Opportunity Statement:
ICON is committed to inclusive hiring practices. All qualified applicants will receive consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. Reasonable accommodations are available upon request for candidates with disabilities.

For more information about ICON and career opportunities, visit www.iconplc.com.