Clinical Study Coordinators

Based on our more than 12 years experience in clinical research, our working model incorporates a crucial piece in every successful clinical trial: a well trained, highly experienced study coordinator.

Our study coordinators are fully trained in ICH GCP requirements, standard operating procedures and project specifics to ensure best-in-class quality and speed.

They assist the Investigational site staff with performing some of the test, compiling information, dealing with queries, etc.

This allows the Investigators to concentrate on those tasks that only they can perform, providing an additional mean to reach maximum efficiency.

Whether our client's study is conducted and managed by TransCom or not, we offer our Clinical Study Coordinators to support our client's efforts to bring their studies to successful completion.