Vacancy Description
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...
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...
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