# Clinical Research Associate

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

**Apply**: https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/So-Paulo/CRA-I---II---Oncology-Projects_252852-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_0683e678-879

## Description

We are seeking a Clinical Research Associate to manage clinical studies according to Fortrea's Standard Operating Procedures, ICH GCP Guidelines, and Sponsor requirements.

**Responsibilities:**

- Conduct site monitoring responsibilities for clinical trials, including pre-study, site initiation, process monitoring, routine monitoring, and close-out visits

- Prepare and implement project plans related to Clinical Monitoring responsibilities

- Ensure the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to

- Safeguard data integrity by reviewing source documents, generating queries, and resolving issues

- Confirm site regulatory documents and eTMF/Sponsor documents are complete and current

- Ensure adherence to global quality control and CRA performance metrics

- Travel to study sites, which may be required up to 60% of the time

**Requirements:**

- University or college degree in a related allied health profession (e.g., nursing licensure)

- 4-5 years of Clinical Monitoring experience

- Previous experience working with Oncology projects

- Fluent in English and local office language

- Ability to work with minimal supervision

- Understanding of Serious Adverse Event (SAE) reporting and process production

**Preferred Qualifications:**

- Thorough working knowledge of Fortrea SOPs for site monitoring

- Experience in a related field (e.g., medical, clinical, pharmaceutical, laboratory, research, data analysis)

- Phase I monitoring experience

- Life Science or Nursing qualification

- Specific skills, systems, certifications, and/or licenses preferred

**Physical Demands/Work Environment:**

- Must be able to sit at a computer for long periods

- Must be able to use hands to finger, handle or touch objects, tools or controls

- Standard office and/or home working environment

- Clinical Research Unit and hospital environment (administrative only)

- Risk of eye strain

- Will involve outside of normal office hours as required by the role

## Skills

### Required
- ICH GCP Guidelines
- Clinical Monitoring
- Oncology
- English
- Portuguese

### Nice to have
- Fortrea SOPs
- Phase I monitoring
- Life Science
- Nursing
- e-clinical systems

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Source: [Apply at fortrea.wd1.myworkdayjobs.com](https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/So-Paulo/CRA-I---II---Oncology-Projects_252852-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)