# CRA All Levels Unblinded - São Paulo (FSP Sponsor Dedicated)

**Company**: ICON
**Location**: São Paulo
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Brazil-Sao-Paulo/Clinical-Research-Associate_JR157365?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_74a9f486-b00

## 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 Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

**Responsibilities:**

- Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.

- Conduct site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.

- Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.

- Provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.

- Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

**Your Profile:**

- Bachelor's degree in a relevant scientific discipline or healthcare-related field

- Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.

- Proven ability to manage multiple sites and projects simultaneously, with strong organisational and problem-solving skills.

- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.

- Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.

- Willingness to travel as required (approximately 60%)

**Rewards & 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

## Skills

### Required
- Clinical trial monitoring
- Good Clinical Practice (GCP)
- Data integrity
- Site management
- Clinical trial software and tools

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Brazil-Sao-Paulo/Clinical-Research-Associate_JR157365?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)