CLinical Monitoring

Our Clinical Research Associates (CRAs) bring significant experience and expertise with an average 10 years of monitoring experience.  Our teams consists of both employee and contracted CRAs to ensure regional coverage and understanding in the therapeutic area under study.  Our CRAs hold degrees in nursing, medicine or data management with demonstrated proficiency in subject protection, Good Clinical Practices, ICH Guidelines and FDA regulations.  We believe this extensive experience and training is critical to understanding the complexities in the clinical arena. 

Our Expert CRAs

 

  • Investigator Identification and Selection
  • Site Qualification
  • Site Initiation
  • Periodic Monitoring
  • Closeout Visits
  • Co-monitoring
  • Pre-inspection Preparation
  • Rescue Missions 
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