Ophthalmic Research Coordinator, TN - (Madison, TN)

Reviews and comprehends all study protocols, e.g., study proceedings and timelines, inclusionand exclusion criteria, confidentiality and privacy protections. Conducts and/or participates in the informed consent process/discussion with researchparticipants, including answering any questions related to the study. Obtains appropriatesignatures and dates on forms in appropriate places per the research SOP. Assures thatamended consent forms are appropriately implemented and signed respectively. Screens subjects for eligibility using protocol specific inclusion and exclusion criteria,documenting each potential participant's eligibility accurately. Facilitates and coordinates the daily clinical trial activities Performs venipuncture to collect blood samples Certified Clinical Research Coordinator or Professional (CCRC/CCRP) is preferred. Certified Ophthalmic Assistant or Certified Ophthalmic Technician is preferred.