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Senior Pharmacovigilance Associate

100% remote Flexible hours Hiring now

About the position Senior Pharmacovigilance Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a Senior Pharmacovigilance Associate at ICON, you will be instrumental in ensuring the safety and efficacy of pharmaceutical products by managing and oversee pharmacovigilance activities.

Responsibilities

  • Leading the collection, evaluation, and processing of adverse event reports to ensure timely and accurate reporting in accordance with regulatory guidelines and company policies.
  • Conducting thorough data analysis and interpretation of safety data, identifying trends and potential safety signals that require further investigation.
  • Preparing and submitting comprehensive periodic safety update reports (PSURs) and other regulatory documents, ensuring compliance with international regulations.
  • Collaborating with medical and clinical teams to assess the clinical relevance of reported adverse events and contribute to risk management activities.
  • Overseeing the maintenance and integrity of pharmacovigilance databases, ensuring accurate documentation and compliance with data management standards.
  • Providing training and mentorship to junior team members on pharmacovigilance processes, regulatory requirements, and best practices.
  • Engaging in audits and inspections conducted by regulatory authorities, ensuring readiness and compliance with all relevant pharmacovigilance requirements.

Requirements

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience in pharmacovigilance or drug safety, with a strong understanding of relevant regulations and industry standards.
  • Proven ability to manage the pharmacovigilance process effectively, including adverse event reporting and signal detection.
  • Strong analytical and critical thinking skills, with the ability to interpret complex data and make informed recommendations.
  • Advanced level of English
  • Based in Sao Paulo - 100% Remote
  • Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Benefits

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

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