Consulting

Our Research Coordinator will spend several days at your site, which will consist of reviewing the protocol and assisting your staff with source documentation preparation and proper documentation and review of your regulatory binder. We will also assist in how to review a Protocol to look for hidden costs that can affect your budget. Also, things you should always ask for when negotiating your budget.

In addition, our Research Coordinator will spend time with your dedicated Research staff to guide you through the proper handling and documentation process of a patient visit.

Such as:

  • Training/Assistance with proper handling of specimens and lab sample processing.
  • Assist with patient flow to ensure efficient utilization of both the coordinators time and the Physicians.
  • Review proper Drug handling and storage guidelines.

SGM will also provide Standard Operating Procedure templates that can be adjusted to fit your needs. We will also provide sample source forms for current medications, Adverse Events, Physical Exams forms, Temperature logs, Informed Consent Documentation process.

For more information, please contact Lucinda Little, CCRC at 610-999-3437 or at llittle@sgmprc.com