Oncology Clinical Research Associat

Responsibilities: of the Oncology Clinical Research Associate (CRA): · Perform site selection, site initiation, routine monitoring, and close-out visits while ensuring compliance with Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines. · Partner with investigative sites to create, implement, and monitor patient recruitment strategies that align with study timelines and project objectives. · Deliver protocol-specific training and maintain ongoing communication with site personnel to ensure expectations are clear and challenges are addressed proactively. · Assess site performance and processes to ensure adherence to study protocols, identifying and escalating quality or compliance concerns when necessary. Requirements of the Oncology Clinical Research Associate (CRA): · Minimum 3+ years of on-site monitoring experience within Oncology clinical trials. · Strong knowledge of GCP and ICH regulations, along with demonstrated expertise in oncology clinical trial protocols. · Bachelor's degree in a scientific, healthcare-related, or equivalent discipline preferred. Compensation: & Benefits · Salary Range: $110,000 - $130,000 · Comprehensive Benefits: Medical, Dental, Vision, 401(k), Paid Time Off, Sick Leave (as required by law), and Paid Holidays