Job Description
Serve as, or assist, Study Coordinator in all facets of protocol; conduct patient and caregiver interviews, interact with families and pharmaceutical sponsors. Collect and maintain data and complete case report records; dispense medication and monitor drug log inventory; follow up on adverse events; perform lab duties, e.g. venipuncture, urine, vital signs, ECGs. Must have a medical background in placing and managing IVs. RN or LPN preferred. Complete and maintain regulatory documents. Communicate with and implement instructions from Principal and/or Sub-Investigator. Must have excellent computer skills and experience in electronic data entry. Fluent in English & Spanish.
Job Requirements
Our Clinical Drug Trial Practice is looking for individuals with a medical background in placing and managing IVs and with clinical research and study coordinator experience. ONLY EXPERIENCED CANDIDATES NEED APPLY. Certification preferred. Job requires minimal supervision.
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