Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Pharmacovigilance Associate

Pharmiweb
pharmiweb
1-3 years
Not Disclosed
Brazil, Remote
10 March 18, 2026
Job Description
Job Type: Full Time Remote 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

Company: ICON Strategic Solutions (ICON plc)
Location: Brazil (Remote/Home-Based – São Paulo)
Job Type: Full-Time
Salary: Competitive
Posted Date: 17 March 2026
Application Deadline: 16 April 2026

Job Overview
ICON Strategic Solutions, a globally recognized leader in healthcare intelligence and clinical research, is seeking a Pharmacovigilance Associate to join its high-performing safety team. This role offers an excellent opportunity for professionals looking to build or advance their career in pharmacovigilance, drug safety, and regulatory compliance within a global CRO environment.

The selected candidate will be responsible for monitoring the safety of pharmaceutical products through accurate collection, evaluation, and reporting of adverse event data. This position plays a key role in ensuring compliance with international regulatory standards and supporting patient safety initiatives.

Key Responsibilities

  • Collect, review, and process adverse event (AE) reports in compliance with global pharmacovigilance guidelines

  • Ensure timely and accurate safety data reporting to regulatory authorities

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

  • Collaborate with cross-functional teams including clinical operations, regulatory affairs, and medical teams

  • Assist in the preparation and submission of individual case safety reports (ICSRs) and aggregate reports

  • Maintain up-to-date knowledge of global pharmacovigilance regulations and best practices

  • Support safety investigations, audits, and regulatory inspections

Required Qualifications and Experience

  • Bachelor’s degree in Life Sciences, Pharmacy, or a related discipline (Master’s preferred)

  • Experience Required: 1–3 years of experience in pharmacovigilance, drug safety, or clinical research

  • Strong understanding of pharmacovigilance processes and global regulatory requirements (ICH, GVP)

  • Excellent analytical, documentation, and data interpretation skills

  • High attention to detail with strong organizational abilities

  • Advanced proficiency in English (written and verbal)

  • Ability to work independently in a remote, home-based setup

Preferred Skills

  • Experience with safety databases such as Argus Safety or ARISg

  • Familiarity with global regulatory agencies (FDA, EMA)

  • Strong communication and teamwork capabilities

Why Join ICON Strategic Solutions
ICON fosters a culture of innovation, inclusion, and continuous learning. Employees are empowered to contribute to global clinical development programs while benefiting from a supportive and growth-oriented work environment.

Compensation and Benefits

  • Competitive salary package

  • Generous annual leave and paid time off

  • Comprehensive health insurance for employees and dependents

  • Retirement planning and savings programs

  • Global Employee Assistance Programme (LifeWorks) with 24/7 support

  • Life insurance coverage

  • Flexible benefits including childcare support, wellness initiatives, and travel assistance

  • Access to health assessments and discounted fitness memberships

Diversity and Inclusion
ICON is an equal opportunity employer committed to building a diverse and inclusive workforce. All qualified applicants will receive fair consideration regardless of race, gender, religion, disability, or other protected characteristics.

Application Process
Candidates interested in pharmacovigilance careers and drug safety roles are encouraged to apply. Applicants who may not meet all requirements are still welcome, as ICON considers talent for multiple roles across its global network.

SEO Keywords: Pharmacovigilance Associate Jobs, Drug Safety Jobs Brazil, Remote PV Jobs, Clinical Research Jobs, ICON Careers, Adverse Event Reporting, ICSR Processing, Signal Detection, Pharmacovigilance Careers Global