Per Diem Clinical Research Assistant

• Consents and enrolls patients for research studies by providing detailed information on the Research Study to patients and families
• Is responsible for understanding and adhering to all policies and procedures and responds to all inquiries
• Obtains informed consent and enrolls patients in research studies
• Reviews clinical information to identify patients meeting study inclusion criteria
• Serves as liaison to the families/patients in the research studies, conducted at both on site and off-site locations, guiding and advising them throughout each phase of the study
• Coordinates follow up visits as necessary
• Acts as a resource to study participants, addressing any concerns they may have
• Troubleshoots resolution of any issues that may arise throughout the study
• Coordinates and prepares documentation needed for Institutional Review Board (IRB) on submissions, for PI approval
• Tracks progress from submission to approval
• Assist in developing supportive study documents such as informed consent forms, monitoring templates, study subject tracking tools, monitoring forms, study manuals, and training materials, as required for a study
• Assist with the tracking and compilation of enrollment information
• May assist with preparation of manuscripts and reports to be submitted to academic journals
• May help train and orient newly hired study personnel

A bachelor’s degree in a related field

• flexible schedules
• affordable health, vision and dental insurance
• child care and student loan subsidies
• generous levels of time off
• 403(b) Retirement Savings plan
• Pension
• Tuition and certain License and Certification Reimbursement
• cell phone plan discounts
• discounted rates on T-passes