Support clinical research activities across all phases of study development and execution. Responsibilities include completion of required research compliance and training; assisting with institutional review board (IRB) submissions and documentation; identifying and screening eligible study cases; conducting electronic medical record chart reviews to extract and enter study variables into data management software; performing basic statistical analyses; and contributing to dissemination of findings through abstract and manuscript development for presentation and publication.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Career Level
Intern
Education Level
Ph.D. or professional degree