São Paulo, Brazil Remote (City) Full-time

ICON plc is hiring a Clinical Research Associate All Levels

About the Role

Oversee and support clinical trial execution by managing key site activities including qualification, initiation, monitoring, and close-out visits. You will ensure adherence to study protocols, regulatory standards, and ICH-GCP guidelines while safeguarding patient well-being and data integrity.

Key Responsibilities

  • Lead on-site and remote monitoring activities across multiple trial phases, ensuring compliance and accurate reporting
  • Collaborate with investigators and clinical staff to resolve issues and maintain consistent study conduct
  • Review clinical data for completeness and accuracy, addressing discrepancies promptly
  • Support the development and review of essential study documents such as protocols, monitoring reports, and clinical study summaries
  • Maintain up-to-date regulatory files and ensure inspection readiness at all stages

What You’ll Bring

  • A bachelor’s degree in a life science or healthcare-related discipline
  • At least two years of hands-on experience in clinical monitoring or related field
  • Familiarity with international regulatory requirements and clinical trial workflows
  • Strong written and verbal communication skills, with a focus on precision and clarity
  • Proven ability to manage multiple priorities independently while meeting deadlines
  • Willingness and ability to travel frequently—domestically and internationally—up to 60% of the time
  • Valid driver’s license required for site visits

What We Offer

We support our team through comprehensive benefits, including flexible leave policies, health coverage options, retirement planning tools, and life assurance. Access to a global employee assistance program ensures personal and family well-being is supported 24/7. Additional country-specific benefits may include subsidized travel, fitness memberships, health screenings, and commuter support.

Work Environment

This role is based in major cities across Brazil, including São Paulo, Brasília, and Porto Alegre. The position requires regular travel to clinical sites. We foster an inclusive, performance-driven culture that values diverse perspectives and promotes professional growth in a respectful, equitable workplace.

Required Skills
Clinical Trial ProcessesICH-GCP GuidelinesRegulatory ComplianceClinical ResearchCommunication SkillsOrganizational SkillsTeam Collaboration Clinical Trial ProcessesICH-GCP GuidelinesRegulatory ComplianceClinical ResearchCommunication SkillsOrganizational SkillsTeam Collaboration
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About company
ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization.
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Posted 3 hours ago