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Clinical Monitoring

From Concept to Closure.

Our dedicated team of Clinical Research Associates (CRAs) have a wide range of experience in all phases and many therapeutic areas of clinical research and can be both site and field-based on a full or part-time basis. All our CRAs monitor the conduct and progress of clinical trials in accordance with Illingworth Research or Sponsor company SOPs, ICH-GCP and local regulatory requirements.

Our CRAs can provide a full range of clinical monitoring services including:

  • Site and Investigator Selection
  • Pre-study site assessment
  • Ethics applications
  • Regulatory applications
  • Preparation of Investigator meetings
  • Initiation meetings
  • Monitoring and report writing
  • Adverse Event monitoring
  • Query resolution
  • Investigational Medicinal Product (IMP) accountability
  • Preparation for study site audit
  • Maintenance of essential documentation
  • Close out visits