Working under the direction of a senior research staff member or principal investigator, the clinical research coordinator will be responsible for the overall coordination of large or complex research projects activities and will perform a variety of research, database 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 creating study protocols and manual of operations, template consent forms, case report form content, and tracking regulatory approvals. The individual will perform other duties such as data monitoring 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 ethics applications and adverse event reporting and ensures protocol compliance. The position may support multiple investigators or studies.
*BA or BA degree with three to five years clinical research experience
*Experienced working independently
*Experience with clinical management software, REDCap SharePoint or OpenClinica a plus