Clinical Research Coordinator-Oncology

Onsite 5 Days
Qualifications

+ MUST HAVE 2 years of experience as a Clinical Research Coordinator (CRC), preferably with complex clinical trials

+ MUST HAVE hands-on experience working directly with patients in a clinical research setting, including GI and oncology populations

+ Experience with complex clinical trials, including multi-step protocols and intensive monitoring requirements

+ Proficiency with electronic data capture (EDC) systems for entering and managing study data

+ Experience performing chart reviews and pre-screening patients for clinical trial eligibility

+ Demonstrated ability to ensure compliance with research protocols and regulatory requirements, including IRB processes

+ Proven ability to manage research databases, case report forms, and study documentation accurately and efficiently

Responsibilities

+ Serve as the primary contact fo...