With a strong scientific background and a long industry experience, ClinSearch project managers (PMs) focus on high quality, timely and on budget execution of your international or your local investigation project dealing with medical devices or medicines.
ClinSearch PMs can rely upon an international team of clinical research associates (CRAs) and assistants of operations for the realisation of operational tasks. Beside their in-depth knowledge of operational management, our PMs are also able to provide you with advices on regulatory questions and prepare regulatory submissions files, to write scientific documents such as protocols, case report forms (CRF) or informed consent forms (ICF), to manage biostatisticians and medical writers. In this way, PMs have an overall view of the project enabling its optimal progress, respecting timelines and budget.
ClinSearch PMs are also committed to maintaining a permanent communication channel with study sponsors so that they are kept informed and in control of their project’s progress. Meetings as well as regular project status reports can be provided in this framework.