Clinical Research Coordinator Position Available In Catawba, North Carolina
Tallo's Job Summary: The Clinical Research Coordinator role involves assisting in operationalizing research study tasks, including recruitment, data collection, and reporting. Responsibilities include participant recruitment, data management, and administrative tasks. Requirements include a high school diploma, 1+ year of CRC experience, and knowledge of EDC and EMR systems. This full-time position supports a major healthcare provider in the US.
Job Description
Clinical Research Coordinator Job Description The Research Coordinator will assist an Investigator, Research Associate, or Project Manager with operationalizing the tasks associated with implementing a research study. This includes a variety of tasks related to recruitment, data collection, data management, and reporting of results. Responsibilities Recruits and consents research participants. Conducts telephone or in-person interviews with participants, including screening for eligibility. Performs follow-up by telephone, e-mail, and/or mail with study participants. Prepares, mails, and processes questionnaires and other study correspondence. Assists 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. May assist with literature reviews for proposal submissions and manuscript preparation. Handles bookkeeping related to study budgets, including ordering supplies, requesting checks for payment, and participant incentives. Performs miscellaneous administrative tasks such as typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files. Essential Skills High school diploma or General Education Development (GED) 1+ year of Clinical Research Coordinator (CRC) experience Experience with chart review and patient recruitment Knowledge of EDC and EMR systems Understanding of clinical research and Good Clinical Practice (GCP) Experience in pre-screening patients Qualifications Vaccine experience is a plus Phlebotomy experience is a plus Work Environment This position requires five days on-site work, totaling 40 hours per week. The role supports one of the leading healthcare providers in the US and offers opportunities for advancement within the organization.
