Assoc CRA • Monitoring

Location: São Paulo, Brazil

Company

IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Complete therapeutic, protocol, and clinical research training to support clinical monitoring activities.
• Perform site selection, initiation, monitoring, and close-out visits under close supervision and in accordance with study protocols, standard operating procedures, and Good Clinical Practice.
• Support assigned sites through study training, regular communication, issue management, and evaluation of site quality and protocol compliance.
• Track regulatory submissions and approvals, recruitment and enrollment, Case Report Form completion, and data query resolution.
• Maintain Trial Master File and Investigator Site File documentation and prepare monitoring reports, follow-up letters, and action plans.
• Collaborate with study teams and support site recruitment planning and progress tracking.

Requirements

• Bachelor’s degree in a scientific discipline or healthcare preferred; equivalent education, training, and experience may be accepted.
• Prior clinical experience is preferred.
• Good command of English is required.
• Knowledge of Good Clinical Practice, International Conference on Harmonization guidelines, applicable clinical research regulations, and protocol requirements.
• Proficiency with Microsoft Word, Excel, PowerPoint, and relevant laptop and mobile devices.
• Strong attention to detail, communication, organization, judgment, problem-solving, and relationship-building skills.

Culture & Benefits

• Work with a diverse team focused on clinical research and improving patient outcomes.
• Opportunities to develop project management abilities and grow professionally.
• Competitive salary and benefits package.
• Full-time employment.