The Clinical Research Specialist I is an entry level position, that applies professional knowledge, skills, and training to conduct clinical research work in a specific discipline. The Specialist works on portions of projects and studies with guidance. Responsibilities include but are not limited to:

•Participate in patient screening and enrollment

•Able to communicate with patients/families, physicians, and research collaborators

•Retrieve and compile data from multiple sources in a timely manner

•Performs entry of study data within the required time allotted per the research study guidelines

•Management of subject case report file to ensure that all consent forms and study information packets are available as needed.

•Preparing and maintaining regulatory binders

•Assists in preparing data for adverse event reporting and IRB submissions