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Pharmacovigilance Associate

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ICON
Freshers years
Not Disclosed
Argentina, Remote, USA, Remote
9 May 7, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICD-10 CM, CPT, HCPCS Coding, 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
Company: ICON plc (ICON Strategic Solutions)
Location: Buenos Aires, Argentina (Remote / Homeworking)
Start Date: 6 May 2026
Application Deadline: 5 June 2026
Employment Type: Full-Time
Work Mode: Remote


Job Overview

This role is part of a global pharmacovigilance and drug safety team responsible for monitoring the safety of pharmaceutical products.

You will be involved in collecting, reviewing, analyzing, and reporting adverse event data to ensure patient safety and regulatory compliance in clinical development and post-marketing settings.


Key Responsibilities

1. Adverse Event Processing

  • Collect and review adverse event (AE) reports

  • Ensure accurate, complete, and timely safety reporting

  • Follow global pharmacovigilance regulatory guidelines


2. Safety Monitoring & Risk Management

  • Conduct signal detection activities

  • Perform risk assessment for potential safety issues

  • Identify trends and emerging safety concerns


3. Cross-Functional Collaboration

  • Work with clinical, regulatory, and operational teams

  • Support safety-related investigations and queries

  • Coordinate responses to internal and external stakeholders


4. Regulatory Compliance

  • Maintain up-to-date knowledge of:

    • Pharmacovigilance regulations

    • Industry safety guidelines

  • Ensure compliance in all safety reporting activities


5. Safety Reporting Support

  • Assist in preparation of:

    • Safety reports

    • Regulatory submissions

  • Support pharmacovigilance documentation activities


Required Qualifications

  • Bachelor’s degree in:

    • Life Sciences

    • Pharmacy

    • Healthcare-related scientific discipline

    • Or equivalent field


Experience Required

  • Experience in:

    • Pharmacovigilance

    • Drug safety

    • Clinical or pharmaceutical environment (preferred)


Key Skills Required

  • Strong analytical skills

  • High attention to detail in data handling

  • Good understanding of safety reporting processes

  • Strong communication and teamwork abilities

  • Ability to work in regulated environments


Language Requirement

  • Advanced English proficiency (mandatory)


Work Environment

  • Fully remote position (based in Buenos Aires)

  • Global pharmacovigilance operations environment

  • Collaboration with international teams

  • Compliance-driven and quality-focused work setting


Company Overview (ICON plc)

ICON plc is a leading global healthcare intelligence and clinical research organization specializing in clinical development and pharmacovigilance services.

The company focuses on:

  • Clinical trials

  • Drug safety

  • Regulatory support

  • Healthcare intelligence solutions

ICON promotes:

  • Inclusion and diversity

  • High-performance culture

  • Global career opportunities

  • Employee well-being and flexibility


Benefits Overview

  • Paid annual leave

  • Health insurance options (country-specific)

  • Retirement and savings plans

  • Employee assistance programs (global support network)

  • Life insurance coverage

  • Flexible benefits (childcare, transport, gym, health assessments, etc.)