Clinical Research Associate
Current• Co-ordinate non-therapeutic research studies• Assist with protocol development• Submit new protocols and continuing reviews to Institutional Review Board• Prepare submissions for all reportable events (adverse events. protocol variations, etc.)• Ensure compliance with prescribed interventions and evaluations of the assigned protocol(s)• Provide data to the collaborating research organization (CRO) or study sponsor• Develop, maintain, and/or monitor case report forms• Prepare data reports• Perform data abstraction, collection, and entry to support clinical research• Maintain protocol/participant binders• Determine eligibility, recruit and schedule study participants• Release Informed Consent documents• Recruit study participants and conduct informed consent process for non-therapeutic research studies•Administer research questionnaires and enter the data into electronic data capture systems•Abstract data through chart reviews and electronic systems•Assist with protocol development•Design data capture forms•Develop and support research databases•Maintain patient database by recording new patient information and recording and verifying patient admissions, discharges, and admission diagnoses•Generate queries/reports of patient data as required
