• Help the investigator in screening patients
  • Assisting investigators in the Informed Consent Process
  • Coordination and management of laboratory samples, courier and follow-ups of lab reports
  • Drug accountability and dispensing at the site
  • Investigational product management, dispensing, temperature monitoring and accountability
  • Preparation, attendance and follow-up of monitoring
  • Completing CRF entry
  • Preparation, attendance and follow-up of Audit
  • Preparation & forwarding the necessary information of closeout
  • Prepare the required documents for submission to the Ethics Committee
  • Initiating and submitting for Ethics Committee approval


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