Site Management

Our site management team bridges the gap between sites and sponsor/CRO in accelerating patient enrollment and effectively managing the trial from start to finish; thus ensuring smooth transit of the trials to the next phase.
With 6 regional offices across India and presence in other Asia Pacific countries, we provide access to more than 500 sites and a large network of highly qualified investigators.
Our site support model involves placement of highly qualified and trained clinical research coordinator (CRC) at each study site to assist the investigator and site staff with all day-to-day study activities.
The roles and responsibility of CRC includes:

  • Protection of research subjects
  • Ensuring accurate of data
  • Regulatory submissions
  • Site preparation for the clinical trial
  • Additional staff training
  • Interacting with EC/CRO/Labs/Sponsor/PI
  • Maintaining clinical trial documents/records
  • IP accountability
  • Scheduling patients’ visits and ensuring retention till study completion
  • Keeping the investigator informed and compliant