Apply for IQVIA Pharmacovigilance Specialist job in Mexico City. Work remotely in clinical research with English, Spanish & French fluency. High-paying global healthcare jobs 2025.
IQVIA Hiring Pharmacovigilance Specialist (Remote Clinical Research) – Apply Now for Global Healthcare Careers 2025
Are you ready to advance your career in the fast-growing field of pharmacovigilance? Global healthcare leader IQVIA is actively hiring a Pharmacovigilance Specialist (Clinical Research) for a full-time, remote position based in Mexico City, Mexico. This trilingual opportunity (English, Spanish, and French) allows you to work from home while contributing to life-changing medical research and supporting patient safety worldwide.
🌍 About IQVIA — A Global Leader in Clinical Research
IQVIA is one of the world’s largest providers of advanced analytics, technology solutions, and clinical research services for the life sciences industry. Operating in 100+ countries, IQVIA combines human data science, AI-driven solutions, and healthcare intelligence to accelerate drug development and improve global health outcomes.
As a Fortune 500 company, IQVIA partners with top pharmaceutical, biotech, and medical device companies to deliver high-quality clinical research, pharmacovigilance, and real-world evidence services.
🚩 Job Overview: Pharmacovigilance Specialist (Remote)
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Position Title: Pharmacovigilance Specialist (Clinical Research)
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Job ID: R1479248
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Location: Mexico City, Mexico (100% Home-Based)
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Employment Type: Full-Time
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Languages Required: English, Spanish, French (Fluency mandatory)
🔎 Key Responsibilities
Safety Data Processing
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Collect, track, and process Adverse Events (AEs) and safety data according to global regulatory standards.
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Perform database entry, AE coding (MedDRA), and product coding (WHO Drug Dictionary).
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Write case narratives for clinical safety reports.
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Conduct literature surveillance and pharmacovigilance activities.
Medical Review (If Assigned)
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Perform medical review of non-serious AEs and Adverse Drug Reactions (ADRs).
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Assess causality, expectedness/listedness, and data accuracy.
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Maintain documentation of safety evaluations and communications.
Compliance and Quality
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Adhere to IQVIA SOPs, global regulations, and project-specific guidelines.
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Meet productivity, quality, and delivery standards.
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Complete assigned e-trainings and maintain updated training records.
Collaboration
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Work closely with cross-functional teams: project management, data management, clinical monitoring, and medical monitors.
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Serve as a mentor to new pharmacovigilance team members.
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Support client communication for case processing activities.
Additional Duties
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Participate in process improvement initiatives.
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Contribute to departmental audits and inspections.
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Provide pharmacovigilance support across multiple therapeutic areas.
🎯 Qualifications & Eligibility
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Education: Bachelor’s degree in Life Sciences or related field (mandatory).
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Language Skills: Fluency in English, Spanish, and French (mandatory).
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Experience:
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Minimum 1 year of pharmacovigilance experience preferred.
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Clinical research or safety data processing exposure is a plus.
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Technical Skills:
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Proficiency in Microsoft Office (Word, Excel, Outlook).
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Experience with pharmacovigilance software or safety databases preferred.
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📄 Documents Required
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Updated CV mentioning Job ID: R1479248
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Educational certificates (Bachelor’s degree in Life Sciences)
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Proof of language proficiency (if available)
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Previous experience certificates (pharmacovigilance/clinical research)
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Government ID documents (Aadhar, PAN, or local equivalent)
💼 Why Join IQVIA?
🌎 Global Impact
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Contribute to drug safety and global clinical trials in over 100 countries.
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Help bring innovative medical treatments to market faster.
💰 High-Paying Remote Pharmacovigilance Jobs
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Attractive salary packages for trilingual candidates.
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Performance-based incentives and bonus opportunities.
🏠 100% Remote Work Flexibility
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Fully remote role offering excellent work-life balance.
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Glassdoor rating of 4.3/5 for flexibility.
📈 Career Growth & Training
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Continuous professional development through IQVIA’s learning platforms.
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Opportunities to move into global pharmacovigilance leadership roles.
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78% of employees recommend IQVIA for career advancement.
🌐 Industry Leadership
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Be part of a Fortune 500 company leading the AI-driven healthcare revolution.
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Collaborate with top pharmaceutical companies and medical innovators.
📩 How to Apply
Qualified candidates fluent in English, Spanish, and French can apply by:
✅ Online Application:
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Apply directly at jobs.iqvia.com using Job ID: R1479248
✅ Email Application:
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Send your CV and documents to recruitment@iqvia.com with subject line:
“Pharmacovigilance Specialist – R1479248”
Note: Apply promptly as global roles may close quickly due to high demand.
🌟 Build Your Global Pharmacovigilance Career with IQVIA
Pharmacovigilance is one of the most in-demand fields within clinical research and drug development. With rising global regulatory requirements and patient safety standards, companies like IQVIA are continually expanding their global pharmacovigilance teams.
If you have the required language skills and passion for patient safety, this remote IQVIA Pharmacovigilance Specialist position offers a rare opportunity to work with international clients, contribute to global healthcare solutions, and grow within a Fortune 500 organization leading the digital transformation of healthcare.
👉 Apply now and take your pharmacovigilance career global with IQVIA.
✅ Official Career Site: https://jobs.iqvia.com
