Site Coordinator Staffing Support

Several clinical trials are delayed to meet the recruitment deadline and thereby, are subject to incur increased overall costs indirectly.

Clinox ascertains an accelerated approach towards the recruitment of patients. It all begins with the selection of the most relevant sites where odds of recruiting the desired patient population in the shortest timespan is indicated by our structured feasibility.

We also utilize several tools and processes with respect to our sites and clients to accelerate the recruitment of patients. Post recruiting, Clinox takes special efforts to help the patients with retention and compliance. From customized retention programs to prompt travel reimbursements, Clinox takes care of it all in the most efficient manner.

Review of site facility, resources, source documentation practices, EC’s SOP etc. and up-scaling (as and where required) to meet the ICH-GCP and applicable regulatory requirements (Schedule-Y).

Identification and development of potential Principal Investigator(s) (PIs)

Assistance in the execution of Undertaking by the Investigator (Appendix-VII of Schedule-Y), Form FDA 1572, Financial Disclosure, Clinical Trial Agreement etc.

Communication with study Sponsor/CRO

Translation and validation of ICF in required vernacular language(s).