Key Responsibilities

Conduct site selection, initiation, monitoring, and close-out visits
Ensure GCP, protocol, and regulatory compliance
Act as primary contact for sites and investigators
Perform SDV, data review, and query resolution
Oversee investigational product and site documentation
Support investigator meetings and study timelines
Contribute to site training and mentoring of junior CRAs

Your Profile

2+ years CRA experience with monitoring
Oncology experience required
Strong knowledge of GCP/ICH guidelines
Excellent communication and stakeholder management skills
Ability to work independently across multiple sites
Fluent Portuguese
Willingness to travel extensively within Brazil (São Paulo, Goiânia, Porto Alegre, Rio de Janeiro, Salvador)

If this role sounds of interest, please apply today!

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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

CRA Freelance - Brazil