with the Clinical Research Coordinator, principal investigator, members of practice, study sponsors and monitors to provide guidance on the administration of the compliance, financial, personnel, and other related aspects of all ongoing clinical studies. The role requires extensive interaction with patients, physicians, and other office staff and sponsor representatives.
Our Practice typically has five to seven ongoing studies at all time. The Clinical Research Assistant will also be trained as an Ophthalmic Technician which will be vital in performing the study visits. For a detailed list of skills, abilities, responsibilities, and requirements please see the attached job description.
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