As a member of the Clinical Data Team, this position’s primary responsibility will be to research, analyze, and validate clinical information to ensure consistency, integrity, and accuracy based on project specific guidelines. Other responsibilities will include :

• Reviewing and interpreting hospital records (physician notes, pathology reports, and laboratory reports).
• Identifying potential trial patients that meet complex research criteria.
• Performing additional clinical research using the site-specific EMR as needed.
• Communicating with site coordinators regarding any missing clinical information or collection issues.
• Ensuring compliance among site coordinators in clinical information entry and document redaction standards.
• Maintaining confidentiality of patient identification and medical information.
• Communicating with the project managers and clinical data analysts regularly concerning the availability of patients each week that fit project criteria, the status of any outstanding request for clinical information.
• Building and maintaining a good working relationship with colleagues in the Premier Support Team and CBio.