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.
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.