Clinical Research Coordinator

• Working with Principal Investigators (PIs) to facilitate and coordinate the everyday activities of assigned clinical trials including scheduling patient visits with many different departments e.g. Physical Therapy, Radiology, and Anesthesia
• Attending and organizing all study visits with the participant and family
• Monitoring for Adverse Events with study participants, and reporting them to the PI, IRB and sponsor in a timely manner
• Facilitating communication between the PI and the patients
• Maintaining study protocol documents for applications or amendments to the IRB
• Ensuring that all staff involved in the study have been trained properly
• Coordinating with study sponsors and monitors to ensure compliance with the protocol and reporting protocol deviations
• Maintenance of regulatory binders, Case Report Forms, Visit Order forms and other study related documentation. Ensuring patients are reimbursed for their visits
• Recruiting, screening and consenting patients to studies
• Data entry and resolution to data entry queries
• Create and prepare data collection statistical reports and analytical summaries for distribution to the study research team for review and analysis
• May write articles and summaries of studies for submission
• May present study results at local and national meetings
• Mentoring CRA’s, residents, fellows in day to day of clinical research

• A Bachelor’s Degree is required
• 2 years of relevant experience is required

Master’s Degree is preferred

• 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