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From the employer's careers site First seen 11 Nov 2026

CRA I

ICON Sao Paulo, Brazil Remote entry full-time

The employer hasn't listed a salary.

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Description

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 CRA I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.

Responsibilities

Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders.

  • Perform site qualification, initiation, monitoring and closeout activities as assigned.
  • Verify protocol, GCP and regulatory compliance and participant protection.
  • Review source data, essential documents and site processes for accuracy and completeness.
  • Identify and follow up findings, risks and corrective actions.
  • Maintain clear communication with investigators, site staff and study teams.

Required qualifications and experience

  • Relevant life sciences, healthcare or clinical research qualification, or equivalent relevant clinical research experience.
  • Knowledge of ICH Good Clinical Practice (GCP) guidelines and the expertise to review and evaluate medical data.
  • Knowledge of ICH Good Clinical Practice (GCP), clinical trial conduct and site monitoring requirements.
  • Practical experience with site monitoring or site management appropriate to the level of role.
  • Experience performing site qualification, initiation, monitoring and closeout activities as assigned.
  • Experience verifying protocol, GCP and regulatory compliance and participant protection.
  • Experience reviewing source data, essential documents and site processes for accuracy and completeness.

Preferred qualifications and experience

  • Therapeutic area expertise relevant to assigned studies.
  • Experience with risk based monitoring or centralised monitoring approaches.
  • Experience with clinical trial management systems (CTMS), electronic data capture (EDC) and electronic trial master file systems.

Working conditions

  • Willingness to travel as required (approximately 60%).

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

  • 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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Skills

Required

  • ICH Good Clinical Practice (GCP)
  • clinical trial management
  • site monitoring
  • medical data evaluation

Nice to have

  • Therapeutic area expertise
  • risk based monitoring
  • centralised monitoring approaches
  • CTMS
  • EDC
  • electronic trial master file systems

Ready to apply?

You apply with the employer directly. Their original posting is here: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Brazil-Sao-Paulo/CRA-I_JR164235

Apply on ICON