Clinical Monitoring

  • Our monitoring team consist of adequately qualified clinical research professionals, possessing relevant experience and knowledge of GCP guidelines, applicable SOPs, laws, and working practices.
  • We provide personnel both in Clinical Trial Administration cathegory (CTA) and in Clinical Monitoring cathegory (CRA). All clinical research personnel are taking part in an excellent ongoing clinical training programmes.
  • Meeting projected enrollment within required timelines while producing the highest data quality is granted by outstanding relations with investigators based on long history working with our CRAs.
  • All our CRAs possess excellent communication and organization skills, high attention to detail, are flexible and able to prioritize, and are fluent in both spoken and written English.
  • Riddle Research offers clinical monitoring services as a part of full service clinical project, or as a customized standalone service on a „rent-a-monitor“ basis.