Clinical trial staff support

In order to avoid delay in trials we have a diverse team of well qualified, trained, experienced Clinical Research Associates and clinical research coordinators. Our CRCs helps us in the following areas:

• Taking informed consent form with investigators.
• Completion of CRFs.
• Completing of source documents.
• Patient Follow up and query resolution
• Involved in all communications with Ethics committee, CROs/Sponsors, SMOs and site CRAs.
• Coordinate logistics management
• Central and local lab co ordinations