GENERAL SUMMARY OF POSITION:
Under the supervision of the Principal Investigator or designee, the Clinical Research Assistant is responsible for performing delegated tasks and procedures involving human subjects in support of clinical research protocols.
-Assist PI in development of protocol-specific tools to aid in study documentation
-Assess eligibility of research subjects in accordance with the approved protocol and all applicable regulations including HIPAA
-Obtain patient consent and Human Subject Committee approvals for minimal-risk studies as delegated by IRB-approved protocol
-Collect, record, evaluate, update, and store/transport pertinent data and samples in relation to protocol
-Track study enrollment and completion of milestones
-Summarize research findings and prepare presentations
-Perform literature searches
-Schedule patient tests and/or interviews
-Conduct patient telephone follow up
-Stock, inventory, store, and order samples/supplies as needed to maintain appropriate operations
-Review medical records and medical record abstractions for consistency and completeness
-Comply with established policies, health and safety regulations and requirements, procedures, and department objectives
-Maintain patient and study subject confidentiality
-Perform other duties as required.
-Bachelor’s degree in a scientific or health care field, or related experience
-Experience in using computer-based tools (Word, Excel, Access, Outlook, PowerPoint, etc.)
-Oral and written communication skills
-Excellent organizational and interpersonal skills required.
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