Clinical Research Coordinator
Current• Collaborate with PI on preparation and submission of documents required by IRB• Participate in development of relevant internal research procedures.• Maintain study documents including clinical procedures, critical values reporting, and patient informed consent where applicable.• Participate in study site visits upon sponsor request• To ensure that Good Clinical Practices (GCP) and Good Lab Practices (GLP) are met during receipt, processing, storage and return of Clinical Research Samples.• Utilize data management tools to analyze, query, manipulate and correct data according to defined business rules and procedures to ensure source data verification of test results provided to research sponsors.• Perform data preparation and analysis for assigned internal research projects.• Assist in the drafting and submission of Abstracts, Manuscripts, and relevant Marketing material.
