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Pharmacovigilance Associate

Pharmiweb
pharmiweb
1-3 years
Not Disclosed
Remote
10 March 21, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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 – Drug Safety & Risk Management

Location: Buenos Aires, Argentina (Remote/Home-Based)
Job Type: Full-Time
Company: ICON Strategic Solutions
Experience Required: 1–3 Years

Job Overview
ICON Strategic Solutions is seeking a Pharmacovigilance Associate to join its global clinical research and healthcare intelligence team. This role is critical in ensuring the safety and compliance of pharmaceutical products through effective monitoring, evaluation, and reporting of adverse events. The ideal candidate will have a strong foundation in drug safety, regulatory compliance, and clinical research processes, contributing to patient safety and global pharmacovigilance operations.

Key Responsibilities
Collect, review, and process adverse event (AE) and serious adverse event (SAE) reports in compliance with global regulatory requirements
Ensure accurate and timely safety data reporting to regulatory authorities and stakeholders
Conduct signal detection and risk assessment activities to identify potential safety concerns
Assist in the preparation of safety reports, including periodic and aggregate reports for regulatory submissions
Collaborate with cross-functional teams including clinical operations, regulatory affairs, and medical teams for safety evaluations
Maintain pharmacovigilance databases and ensure data accuracy, completeness, and consistency
Support safety-related investigations and respond to internal and external safety queries
Stay updated with global pharmacovigilance regulations, guidelines, and industry best practices

Qualifications
Bachelor’s degree in Life Sciences, Pharmacy, or a related field
Advanced degree (MSc, PharmD, or equivalent) preferred

Experience
1 to 3 years of experience in pharmacovigilance, drug safety, or a related clinical research role
Experience in handling adverse event reporting and safety databases preferred

Skills and Competencies
Strong understanding of pharmacovigilance processes and global regulatory requirements
Excellent attention to detail and analytical skills
Effective written and verbal communication skills in English (advanced level required)
Ability to work independently in a remote environment while managing multiple priorities
Strong teamwork and collaboration abilities

Work Environment
Remote/home-based role located in Buenos Aires, Argentina
Flexible work environment supporting work-life balance

Compensation and Benefits
Competitive salary package aligned with industry standards
Comprehensive health insurance options for employees and families
Retirement planning and financial wellness programs
Global Employee Assistance Program for mental health and well-being support
Life insurance and additional country-specific benefits such as wellness programs, travel support, and lifestyle benefits

Why Join ICON Strategic Solutions
ICON is a globally recognized leader in clinical research and healthcare intelligence, offering professionals the opportunity to work on innovative drug development programs. This role provides exposure to global pharmacovigilance practices, career growth opportunities, and a collaborative environment focused on improving patient safety worldwide.