Clinical Research Associate

Job Summary

To support innovative oncology research, the full-time Clinical Research Associate will oversee clinical trial sites remotely, ensuring compliance with regulatory requirements and high-quality data collection throughout the study lifecycle.

Key responsibilities

• Conduct site selection, initiation, routine monitoring, and close-out visits in accordance with GCP, ICH, and study requirements
• Partner with clinical sites to develop and manage patient recruitment and enrollment strategies
• Monitor study progress, regulatory submissions, data quality, and site performance while identifying and escalating risks

Required qualifications

• 3+ years of clinical research monitoring experience with a focus on oncology studies
• Strong knowledge of Good Clinical Practice (GCP), ICH guidelines, and clinical trial regulations
• Proficiency in Microsoft Office Suite and excellent organizational skills
• Bachelor's degree in a scientific discipline, life sciences, healthcare, or a related field preferred