Reporting to the Clinical Research Director, responsible for managing all aspects of clinical research activity including IRB approval, protocols, case report forms, manuscripts, book chapters, presentations and surgical videos.
1. Coordinate all aspects of assigned research.
a. Submission of protocol amendments, informed consent amendments, HIPAA language modifications for required documents, continuing reviews, and adverse events to the IRB.
b. Screen research participants, obtain informed consent, and administer and complete questionnaires.
c. Recruitment, scheduling, and payment of research participants, as applicable.
d. Maintain research databases, data analysis, data management, data quality assessment.
2. Management of manuscripts and book chapters
a. Conduct literature reviews
b. Assist with data analysis
c. Interface with physicians, statistician and artist as needed
d. Proofread and edit documents as needed
e. Submission of abstracts to various educational meetings
f. Ensure timely submission of manuscript and textbook files to peer-reviewed journals or editorial staff
3. Create and update all PowerPoint presentations and educational videos for the dissemination of research findings
a. Creation of presentations/posters for abstracts accepted to educational meetings
b. Photograph/Film surgeries or clinical visits as necessary
c. Create and edit videos and pictures as necessary
Education: Bachelor’s degree preferred, but not required.
Experience: Research experience preferred, but not required.