Employer Active
Job Alert
You will be updated with latest job alerts via emailJob Alert
You will be updated with latest job alerts via emailSKILLS/ ABILITIES/ COMPETENCIES REQUIRED: (MUST be realistic measurable objective and related to the essential functions of the job.
GENERAL SUMMARY/ OVERVIEW STATEMENT: Summarize the nature and level of work performed.
Under general direction of the principal Investigators the Clinical Research Coordinator II is responsible and accountable for assisting in the implementation of a research protocol using scientific methods including working with physicians clinical nurses and subjects to identify and recruit eligible subjects obtain all necessary approvals and informed consent forms screen and enroll subjects into the study assess subject participation on a continuous basis in light of ethical considerations and act as a liaison between the subject and other members of the team regarding the research protocol. Responsible for data entry of data for the study. Works closely with the physicians involved in the study to contact the subjects and families. Organizes visits and subject family interviews for principal investigators. Logs in all applicable data elements as requested and coordinates information and supply transfer as necessary to complete study elements at multiple sites. Summarizes data and information for review and analysis by the investigators and project team.
x
Required Experience:
IC
Full-Time