Clinical Research Coordinator III
Children's Outpatient Center - Rockville, MD

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This position requires significant prior clinical research experience. The individual will be responsible for the overall coordination of large or complex research projects activities and perform a variety of research, data base and administrative/clerical duties in support of clinical trials in an effort to assist investigators in organizing, gathering and compiling clinical research data. This person is primarily responsible for data collection through patient enrollment, patient or family interviews, medical chart abstraction or other methods. The CRC III will perform other duties such as data entry in addition to being responsible for selected administrative duties such as filing and record keeping, photocopying, creating flyers and posters and maintaining study records. The individual assumes responsibility for the submission and maintenance of ongoing regulatory documents including the preparation of IRB applications and adverse event reporting and ensures protocol compliance. The position may support multiple investigators or studies. The CRC III may assume responsibility for directing the work of Clinical Research Assistants (CRC) or other Clinical Research Coordinator (CRC I-II). The Clinical Research Coordinator III requires minimal supervision and works largely independently. The individual is supervised by a senior research staff member or principal investigator.

BA/BS degree in science, technical, or health-related field with > 4 year relevant experience


MS degree with 2 years relevant experience

1-4 years of clinical and/or research experience or an equivalent combination of relevant education and/or experience


Prior clinical research experience