CRA 1 (Clinical Research)

Location: São Paulo, Brazil

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Conduct site selection, initiation, monitoring, and close-out visits in accordance with study protocols, GCP, ICH guidelines, and regulatory requirements.
• Support subject recruitment planning, tracking, and communication with clinical research sites.
• Deliver protocol and study-related training and manage ongoing expectations and issues with assigned sites.
• Evaluate site quality and protocol adherence, escalating issues when required.
• Track regulatory submissions, approvals, recruitment, enrollment, CRF completion, and data query resolution.
• Maintain TMF and ISF documentation, prepare monitoring reports, follow-up letters, and action plans, and collaborate with study team members.

Requirements

• Bachelor's degree in a scientific or healthcare discipline preferred.
• Excellent written and spoken English required.
• Basic knowledge of clinical research regulations, including GCP and ICH guidelines.
• Good therapeutic and protocol knowledge gained through company training.
• Strong attention to detail, communication, organization, problem-solving, judgment, and decision-making skills.
• Proficiency with Microsoft Word, Excel, PowerPoint, laptops, and applicable mobile devices.

Culture & Benefits

• Work in an innovative organization focused on improving patient outcomes and population health.
• Collaborate with a diverse clinical research team and project stakeholders.
• Opportunities to develop project management abilities and grow professionally.
• Competitive salary and benefits package.