The Clinical Research Administrator facilitates the timely execution and completion of high-quality clinical research by assisting investigators and industry sponsors with all aspects of the clinical research. With extensive knowledge of regulatory requirements, ethical issues, processes for product development and the business side of clinical research, the Clinical Research Administrator ensures that studies are conducted in accordance with the regulatory standards and are GCP compliant.

Please contact us for comprehensive clinical study administration. Our services include, but are not limited to the following: screening of investigators, qualification of clinical sites, budgeting and contracts negotiation, completion of regulatory documents, posing as an IRB (Institutional Review Board) liaison, developing clinical studies quality system documentation and compliance monitoring.