Principal investigators with more than 35 years of combined experience in trials, involved in our trials from the feasibility to the trinings for every staff.
Study coordinators with over 15 years of combined experience and full trained to performance a high quality protocol conduction, individually trained from Principal investigators and sponsor. CRC are responsible for conducting protocol required patient visits, collecting and documenting clinical information as well as making sure that protocol integrity is up held to the highest standards.
Lab Technician has multiple years of experience collecting samples and performing tests to analyze body fluids, tissue, and other substances. They also conduct general support functions within the Specimen Processing Department. They utilize established protocol and procedures, which include setting up specimens and conducting laboratory tests. They are critical to the collection of quality data from subject.