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Pharmacovigilance Associate Post-Marketing (Fsp - Sponsor Dedicated)

1-3 years
Not Disclosed
10 Dec. 16, 2025
Job Description
Job Type: 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)
Employer: ICON Strategic Solutions
Location: Brazil (Remote / Home-Based)
Salary: Competitive
Start Date: 15 Dec 2025 | Closing Date: 14 Jan 2026

About ICON Strategic Solutions:
ICON plc is a global leader in healthcare intelligence and clinical research, committed to innovation, excellence, and patient safety. We offer a collaborative and inclusive work environment where professionals drive clinical development forward and shape the future of healthcare.

Role Overview:
ICON is seeking a Pharmacovigilance Associate – Post-Marketing to join our Brazil-based remote team. In this role, you will play a crucial part in ensuring the safety of marketed pharmaceutical products by collecting, evaluating, and reporting adverse event information in compliance with global regulatory standards. This position is ideal for candidates passionate about drug safety, pharmacovigilance regulations, and patient protection.

Key Responsibilities:

  • Review, collect, and process adverse event reports according to local and global regulatory requirements.

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

  • Collaborate with cross-functional teams to support safety-related inquiries and investigations.

  • Assist in the preparation of periodic safety reports, regulatory submissions, and internal documentation.

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

Candidate Profile:

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

  • Prior experience in pharmacovigilance, drug safety, or clinical case processing is highly desirable.

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

  • Excellent communication and interpersonal skills for effective teamwork and stakeholder interaction.

  • Commitment to high-quality standards, regulatory compliance, and patient safety.

Experience Required:

  • 1–3 years of relevant experience in pharmacovigilance or drug safety case processing.

Why ICON?
ICON prioritizes diversity, talent development, and high performance. Employees benefit from a competitive salary and comprehensive global benefits, including:

  • Flexible annual leave entitlements.

  • Health insurance options covering employees and families.

  • Retirement planning programs.

  • Life assurance and Employee Assistance Programs (EAP).

  • Country-specific optional benefits such as childcare vouchers, gym discounts, and subsidized travel.

Equal Opportunity Employer:
ICON is committed to an inclusive workplace and provides equal opportunities without regard to race, color, religion, gender, sexual orientation, disability, veteran status, or other protected categories. Reasonable accommodations are available for candidates with disabilities.

Application:
If you are motivated to contribute to global drug safety and pharmacovigilance, apply today—even if you do not meet every listed requirement. ICON values potential and encourages all qualified candidates to apply.