CRA I

General Description:

• The CRA I completes the CRA Training Program and assumes responsibility as a primary CRA.
• The role includes conducting site visits and ensuring data quality and patient safety.

Essential Functions:

• Perform and coordinate clinical monitoring processes in accordance with GCPs and SOPs.
• Maintain oversight of site performance and provide protocol training to study sites.
• Collaborate with the Clinical Study Team to achieve study milestones and resolve discrepancies.

Minimum Requirements:

• BS/BA in a relevant scientific discipline; experience in oncology global trials preferred.
• Excellent communication, organizational, and multitasking skills.
• Fluent in English and proficient in Microsoft Word, Excel, PowerPoint, and Outlook.

Working Conditions:

• Remote based in Brazil with up to 70% travel.
• Supervises assigned study sites and may mentor CRAs in training.