CRA in Brazil, Indiana at Jobgether

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a CRA (Clinical Research Associate) in Brazil.

This role is part of a fast-paced clinical research environment focused on advancing global drug development and improving patient outcomes. You will be responsible for ensuring that clinical trial sites operate in full compliance with regulatory requirements, ICH-GCP guidelines, and study protocols. The position involves both on-site and remote monitoring activities, where you will assess site performance, data integrity, and patient safety. You will work closely with investigators and site staff to support smooth study execution, from site initiation through close-out. The role requires strong attention to detail, sound judgment, and the ability to manage multiple priorities in a highly regulated environment. It is an opportunity to contribute directly to the quality and success of clinical studies that impact healthcare worldwide.

In this role, you will oversee the monitoring and management of clinical trial sites, ensuring compliance, data quality, and patient safety across all study phases. You will act as a key liaison between study sites and internal project teams, supporting efficient trial execution and regulatory adherence.

• Conduct site qualification, initiation, monitoring, and close-out visits (on-site or remote)
• Ensure compliance with ICH-GCP, study protocols, and applicable regulatory requirements
• Verify informed consent processes and protect subject confidentiality throughout the study
• Review source documents, case report forms, and resolve data queries in a timely manner
• Assess site performance, protocol deviations, and safety-related issues, escalating when necessary
• Perform investigational product accountability, including reconciliation, storage, and compliance checks
• Maintain and reconcile Trial Master File (TMF) and Investigator Site File (ISF) documentation
• Document monitoring activities through reports, communications, and tracking systems
• Support patient recruitment, retention, and site training activities
• Participate in investigator meetings, study trainings, and audit preparation activities

The ideal candidate has solid clinical research monitoring experience and strong knowledge of regulatory frameworks and clinical trial processes. You are organized, communicative, and able to work effectively in a dynamic, global environment.

• Bachelor’s degree in a health/science-related field or equivalent education/experience (RN or similar accepted)
• Solid understanding of ICH-GCP guidelines and clinical trial regulations
• Previous experience in clinical monitoring or clinical research roles (CRA experience preferred)
• Strong knowledge of source data verification, site management, and clinical documentation practices
• Excellent communication, interpersonal, and stakeholder management skills
• Ability to manage multiple sites and adapt to changing priorities in fast-paced studies
• Proficiency with clinical systems and standard computer tools
• Willingness to travel up to approximately 75% when required
• Strong attention to detail, problem-solving mindset, and high ethical standards

• Competitive compensation package aligned with experience and market standards
• Opportunity to work on global clinical trials impacting patient health worldwide
• Exposure to international teams and leading-edge clinical research practices
• Career development and training in clinical operations and monitoring
• Flexible work arrangements depending on study needs (remote/on-site blend)
• Comprehensive benefits package (health, wellness, and retirement options depending on region)