Medical Assistant

 PURPOSE

The Medical Assistant is responsible for managing an assigned set of research protocols to ensure efficiency and regulatory compliance of the protocol, attending clinic as needed. This position reports to the Site Director (or designee). Responsible for compilation, registration, and submission of data: monitors study compliance and maintains a system for effective data flow associated with research protocols. This position oversees and coordinates the execution of clinical trials including but not limited to, protocol procedures, monitoring follow up visits, overseeing regulatory and administrative details performed by study teams and study close out processes.

QUALIFICATIONS

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.

EDUCATION and/or EXPERIENCE

Minimum Associate’s Degree; Minimum of 2 years of CRC experience;  Experience working in a health care setting, preferably in research.  Experience conducting vitals and EKGs, required.  Strong working knowledge of Clinical Research procedures and guidelines, required. Organizing and coordinating skills, teaching and facilitation skills, ability to assess training needs and objectives. Experience overseeing and coordinating the work of others.

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