Clinical Research Associate

This is a fully remote position, open to applicants in United States.

📋 Description

• Perform qualification, initiation, monitoring, and close-out visits.

• Ensure patient safety, adherence to protocols, and data integrity.

• Analyze source data and study documentation.

• Assist with site activation and study execution activities.

• Foster relationships with investigators and site staff.

• Contribute to initiatives for recruitment and retention.

• Maintain precise documentation and reporting in line with company standards.

• Appropriately escalate study risks and issues.

⛳️ Requirements

• Bachelor’s degree in a scientific or healthcare field.

• At least 2 years of experience in on-site monitoring.

• Strong knowledge of FDA regulations and ICH-GCP guidelines.

• Demonstrated experience in site management.

• Exceptional organizational and communication abilities.

• Willingness to travel extensively within designated regions.

• Preferred experience in renal, nephrology, rare diseases, cardiometabolic, or oncology studies.

🏝️ Benefits

• Competitive salary and customized benefits package.

• Options for hybrid or remote work arrangements based on location and role.

• Opportunities for learning and access to a global network of scientific experts.

• Programs promoting employee well-being and initiatives that support work-life balance, health, and team cohesion.

• Participation in global engagement surveys.

• Recognition programs.

• Team-building activities.

• Experience with a variety of international projects and clients.