Clinical Research Coordinator

The Clinical Research Coordinator (CRC) supports both Site and Sponsor on a variety of Clinical Trials involving pharmaceutical and/or biomedical therapies/treatments. Study support includes a 2 week remote training period & Patient Recruitment and/or Retention duties. Duties can include any of the following tasks depending on the specific assignment. Tasks: Chart review, phone screening, medical record retrieval, appointment scheduling/follow up, data entry, source document uploading, informed consent procedures and more.

Research or Clinical Research Experience Preferred

Clinical/Medical Setting Experience

EMR/EDC experience

Strong administrative skills using computer systems/applications

Able to multiple task and handle challenges with ease