Clinical Research Coordinator Position Available In Rowan, North Carolina

Clinical Research Coordinator Job Description Looking to hire an individual with clinical research experience to act as a consultant CRC to support am ongoing clinical trial. The main job duties for this position will be regulatory filing, creating source documents, data entry (EDC), along with patient recruitment and other research administrative duties. Please note, as the position and study progress, additional job duties will likely be added that are not listed in this description. A candidate must be flexible to help the site and study wherever needed. •This role requires research experience• Responsibilities Recruits and consents research participants. Conducts telephone or in-person interviews with participants, including screening for eligibility. Performs follow-up with study participants via telephone, email, and/or mail. 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 and 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. Main duties will include checking vitals and drawing blood. Essential Skills High school diploma or General Education Development (GED) Experience in chart review, patient recruitment, EDC, EMR, clinical research, and GCP Phlebotomy skills (must be skilled in administering injections.) Interest in growing in clinical research

Recruiter:

Shelby Ciardelli