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 Post-Marketing (Fsp - Sponsor Dedicated)

Icon
ICON
0-2 years
Not Disclosed
10 Dec. 22, 2025
Job Description
Job Type: Full Time Remote 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 – Post-Marketing (FSP – Sponsor Dedicated) | ICON Strategic Solutions
Location: Brazil (Remote / Homeworking)
Salary: Competitive
Start Date: 15 Dec 2025
Application Deadline: 14 Jan 2026

Company Overview:
ICON plc is a global leader in healthcare intelligence and clinical research, committed to advancing patient safety and clinical innovation. We pride ourselves on fostering an inclusive and collaborative environment, where talent is nurtured and excellence is recognized. Join ICON to make a tangible impact on the future of clinical development.

Role Overview:
We are seeking a Pharmacovigilance Associate – Post-Marketing (FSP – Sponsor Dedicated) to join our team in Brazil. This role focuses on the monitoring, evaluation, and reporting of adverse events for pharmaceutical products. You will ensure compliance with international regulatory requirements while supporting patient safety and organizational excellence. This position is ideal for candidates with experience in pharmacovigilance or drug safety seeking to expand their post-marketing expertise.

Key Responsibilities:

  • Collect, review, and process adverse event reports to ensure accurate and timely submissions in line with regulatory guidelines.

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

  • Collaborate with cross-functional and international teams to address safety inquiries and investigations.

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

  • Assist in the preparation of safety reports, regulatory submissions, and documentation for sponsor-specific projects.

Qualifications and Experience:

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

  • Previous experience in pharmacovigilance, drug safety, or clinical data management; experience with case processing is highly desirable.

  • Strong analytical skills, attention to detail, and proficiency in accurate data collection and reporting.

  • Excellent communication and interpersonal skills for effective collaboration with teams and stakeholders.

  • Commitment to maintaining high standards of quality, compliance, and ethical responsibility in pharmacovigilance activities.

What ICON Offers:
ICON values its people and provides a competitive compensation package along with benefits designed to support well-being, career growth, and work-life balance:

  • Comprehensive annual leave entitlements.

  • Health insurance plans tailored to you and your family’s needs.

  • Retirement planning options to secure your financial future.

  • Access to the global Employee Assistance Programme (LifeWorks) providing 24/7 professional support.

  • Life assurance and flexible benefits including childcare support, discounted gym memberships, travel subsidies, and health assessments.

Diversity & Inclusion:
ICON is committed to an inclusive, accessible, and discrimination-free workplace. All qualified applicants receive equal consideration regardless of race, color, religion, gender, sexual orientation, national origin, disability, or veteran status. Reasonable accommodations are available for candidates with medical conditions or disabilities.

Application Note:
Unsure if you meet all requirements? We encourage you to apply – your skills and potential may align with this or other roles at ICON.

Apply Now to join a global leader in post-marketing pharmacovigilance and make a meaningful impact on patient safety.