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Pharmacovigilance Associate Post-Marketing (Fsp - Sponsor Dedicated)

1-3 years
Not Disclosed
10 Dec. 19, 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)

Company: ICON Strategic Solutions
Location: Brazil (Remote / Home-based)
Employment Type: Full-time
Start Date: 15 December 2025
Application Deadline: 14 January 2026
Salary: Competitive, based on experience


Job Overview

ICON Strategic Solutions, a globally recognized leader in healthcare intelligence and clinical research, is seeking a Pharmacovigilance Associate – Post-Marketing (FSP, Sponsor Dedicated) to support post-marketing drug safety activities for a dedicated sponsor.

This role is ideal for professionals with hands-on pharmacovigilance experience who are looking to strengthen their expertise in post-marketing surveillance, safety reporting, and regulatory compliance while working in a fully remote, sponsor-dedicated model.


Key Responsibilities

  • Collect, review, and process post-marketing adverse event reports in accordance with global and local regulatory requirements

  • Ensure accurate, complete, and timely safety data reporting to regulatory authorities

  • Support signal detection, safety surveillance, and risk assessment activities to identify potential safety concerns

  • Collaborate with cross-functional teams to address safety-related queries, follow-ups, and investigations

  • Assist in the preparation and review of aggregate safety reports and regulatory submissions

  • Maintain current knowledge of pharmacovigilance regulations, guidelines, and industry best practices


Required Qualifications and Experience

  • Bachelor’s degree in Pharmacy, Life Sciences, or a related discipline

  • Advanced degree is preferred but not mandatory

  • Experience Required: 1–3 years of relevant experience in pharmacovigilance, drug safety, or post-marketing case processing

  • Proven experience in adverse event case management within a pharmaceutical, CRO, or clinical research environment

  • Strong analytical skills with a high level of attention to detail

  • Excellent written and verbal communication skills

  • Demonstrated commitment to quality, compliance, and patient safety


Preferred Skills

  • Experience working in an FSP (Functional Service Provider) or sponsor-dedicated model

  • Familiarity with global pharmacovigilance regulations and post-marketing safety requirements

  • Ability to work independently in a remote, global team environment


What ICON Offers

ICON’s success is driven by the strength and diversity of its people. The organization provides a collaborative and inclusive work culture that supports professional growth and long-term career development.

Benefits may include:

  • Competitive compensation package

  • Annual leave entitlements aligned with local regulations

  • Comprehensive health insurance options for employees and dependents

  • Retirement and long-term savings plans

  • Life assurance coverage

  • Global Employee Assistance Program (LifeWorks) with 24/7 access to professional support services

  • Flexible, country-specific benefits such as childcare support, wellness programs, gym discounts, travel subsidies, and health assessments


Diversity, Equity, and Inclusion

ICON is committed to fostering an inclusive and respectful workplace. Employment decisions are made without discrimination based on race, gender, age, disability, nationality, sexual orientation, gender identity, or any other protected status. Reasonable accommodations are available throughout the recruitment process.


Why Join ICON?

Even if you do not meet every requirement listed, ICON encourages motivated professionals to apply. This role offers exposure to global post-marketing pharmacovigilance operations, sponsor-dedicated workflows, and long-term career progression within a leading CRO.