Looking for a responsible, computer literate Clinical Research Coordinator with excellent communicative skills. Primary responsibilities include managing clinical trials, the subjects' compliance and well being, informing participants about study objectives, administering questionnaires, adhering to regulatory trial standards, participating in subject recruitment efforts, and other obligations. Must be organized, able to keep multiple files and research trials in order and preferably skilled in blood draws. Experience is preferred. Spanish speaking preferred. Science/research background preferred. Salary depending on experience. Looking for full-time and per diem.
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