Clinical Research Coordinator

Clinical Research Coordinator

Schedule & Travel

Onsite Monday-Friday 8 am-5 pm

Duties

• Assists the CRCs and PIs with all administrative tasks related to clinical research trials
• Conducts telephone or in-person interviews with participants including screening for eligibility
• Performs follow-up for appointments and manages scheduling of appointments (by telephone, e-mail, and/or mail) with study participants
• Prepares, mails and processes questionnaires and other study correspondence
• Assist in tracking study participants using MS Excel
• Keeps accurate and detailed records and files of work
• Reviews, edits, cleans, and enters participant data into a database
• Assists with regulatory management
• May assist with literature reviews for proposal submissions and manuscript preparation
• Bookkeeping related to study budgets (ordering supplies, requesting checks for payment & participant incentives)
• Miscellaneous administrative tasks (typing labels, copying, faxing, meeting preparation, note-taking, transcribing audio files, etc.)

Qualifications

• MUST have a minimum of 1 year of Clinical Research Coordinator
• MUST have experience with EHR/EMR systems
• MUST have experience with Microsoft Office Suite (Outlook, Excel, Word, etc.)
• Customer service experience
• High school diploma or General Education Development (GED) required