About this role
IQVIA is currently recruiting a dedicated Freelance CRA for Brazil.
Location: Brazil, travel within Brazil required FTE: 0.7 Contract: Freelance Start: asap Duration: around 6 months Trials: Phase II Oncology
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.