Sponsors can fully rely on OCT in terms of successful clinical trial conduct from “a” to “z” with a proactive management of timelines and risks. Our specialists are trained to foresee pitfalls and uncertainties:
-due to our vast experience of almost 15 years, we can anticipate many challenges at the study design development stage;
-we always perform a thorough feasibility analysis to ensure a realistic assessment of the possibility to conduct a clinical trial;
-close monitoring of sites allows for reliable quality control.
Our project managers prepare, in a timely manner, a prognosis of possible bottlenecks, analyze tendencies and give recommendations, as well as preparing options to overcome the hurdles. Sponsors determine their extent of involvement in the project and our team takes over all other tasks and responsibilities within the clinical study.
We place high value on effective communication with our clients. To that end, we apply a single-window approach to the “sponsor-project manager” communication flow. Our clients have a single point of contact – a highly competent project manager who provides a timely response and proactive approach. Our project-managers have an average experience of over 5 years in the industry, and many of them have worked for global CROs and Big Pharma.
Clinical trial management system
At OCT, we run our projects in BSI clinical trial management system (CTMS). STREAM is the name of the customized version of CTMS. In addition to a wide functionality aimed at strict compliance of the project with the deadlines, the system includes the eTMF function that allows sponsors to monitor their study online with a 24/7 access from anywhere in the world, which essentially brings the quality of a project’s workflow to a new level.
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