Clinical Research Coordination

As research coordinators, we are entrusted with the responsibility to adhere to each protocol for our Primary Investigator, you the Doctor. The following services are what you can expect from an LFROS Research Clinical Research Coordinator (CRC):

• Create Standard Operating Procedures (SOPs) for your Research
• IRB Preparation/Submission/Qualification
• Staff Protocol Training
• Technician Protocol Training
• Technician Services (if needed)
• Patient recruitment inside and outside of your practice
• Patient Scheduling Per Protocol
• Data Entry
• Continuous Data Review
• A CRC present at each patient visit for your site