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Senior Pharmacovigilance Associate Post-Marketing (Fsp - Sponsor Dedicated)

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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

Senior 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, dedicated to improving patient safety and advancing clinical development. We foster an inclusive and innovative environment, encouraging excellence and collaboration across teams worldwide. Join ICON and contribute to shaping the future of pharmacovigilance and clinical research.

Role Overview:
We are seeking a Senior Pharmacovigilance Associate – Post-Marketing (FSP – Sponsor Dedicated) to manage and oversee pharmacovigilance operations. In this senior role, you will ensure the safety and efficacy of pharmaceutical products through accurate adverse event reporting, signal detection, and regulatory compliance. You will also mentor junior team members and collaborate with cross-functional teams to maintain high standards of patient safety.

Key Responsibilities:

  • Lead the collection, assessment, and processing of adverse event reports, ensuring timely and accurate reporting in compliance with regulatory requirements.

  • Analyze safety data to identify trends, potential risks, and safety signals requiring further investigation.

  • Prepare and submit periodic safety update reports (PSURs) and other regulatory documents in accordance with international guidelines.

  • Collaborate with clinical and medical teams to evaluate the clinical significance of reported events and support risk management activities.

  • Oversee the maintenance and integrity of pharmacovigilance databases, ensuring accuracy and regulatory compliance.

  • Mentor and train junior staff on pharmacovigilance processes, best practices, and regulatory standards.

  • Support audits and inspections conducted by regulatory authorities, ensuring compliance and readiness.

  • Stay updated on evolving regulatory guidelines and industry best practices to continuously enhance pharmacovigilance processes.

Qualifications and Experience:

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

  • Extensive experience in pharmacovigilance or drug safety, including post-marketing surveillance.

  • Strong knowledge of pharmacovigilance regulations, adverse event reporting, and signal detection methodologies.

  • Proven ability to manage pharmacovigilance workflows and ensure compliance with regulatory standards.

  • Strong analytical, problem-solving, and critical thinking skills.

  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.

  • Proficiency in pharmacovigilance databases, data management systems, and Microsoft Office Suite.

  • Ability to work independently, prioritize tasks, and manage multiple responsibilities in a fast-paced environment.

  • Commitment to confidentiality and ethical handling of sensitive patient information.

What ICON Offers:
ICON values its employees and provides a competitive compensation package along with a comprehensive benefits program focused on well-being, career development, and work-life balance:

  • Generous annual leave entitlement.

  • Health insurance coverage for employees and their families.

  • Retirement planning options to secure your financial future.

  • Global Employee Assistance Programme (LifeWorks) offering 24/7 professional support.

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

Diversity & Inclusion:
ICON is committed to fostering an inclusive, accessible, and discrimination-free workplace. All qualified candidates receive equal consideration regardless of race, gender, religion, sexual orientation, 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 expertise and potential may align with this or other opportunities at ICON.

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