Our Clinical Research Associates are effective site managers who oversee and promote an appropriate performance in the sites. Clinical Research Associates perform ongoing interim monitoring, staff training, recruitment guidance, data query resolution, drug and ancillary supply accountability as well as regulatory document review and collection.

Some other activities of the Clinical Research Associates include clinical monitoring reporting, progress tracking and site/sponsor communications.

Our team has strong capabilities which enable them to conduct investigational sites according to the Federal Code of Regulations, GCP guidelines and Standard Operating Procedures.

Our Clinical Monitoring distinctive capabilities include:

  • Deep knowledge of the clinical trial process.
  • Strong scientific background
  • Proved coaching skills.
  • Effective organization, communication and control skills