Clinical Research Coordinator Position Available In Catawba, North Carolina
Tallo's Job Summary: The Clinical Research Coordinator in Hickory, NC, will support CRCs and PIs with administrative tasks for research trials. Responsibilities include interviewing participants, scheduling appointments, tracking data in Excel, and assisting with literature reviews. Qualifications include clinical research experience, EHR/EMR system proficiency, Microsoft Office skills, and 1 year of Phlebotomy experience.
Job Description
Schedule & Travel Onsite in Hickory, NC – 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 Clinical research experience HIGHLY preferred. MUST have experience with EHR/EMR systems MUST have experience with Microsoft Office Suite (Outlook, Excel, Word, etc.) MUST have 1 year of Phlebotomy experience Customer service experience High school diploma or General Education Development (GED) required
