# CRA I

**Company**: ICON
**Location**: Sao Paulo, Brazil
**Work arrangement**: remote
**Experience**: entry
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Brazil-Sao-Paulo/CRA-I_JR164235?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/cra-i-3af76a64-6d0/

## 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

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Brazil-Sao-Paulo/CRA-I_JR164235?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)