staffing and management of institutional review boards, institutional biosafety committees and conflicts of interest; providing administrative support to the officials within the research site who oversee the human subjects research; negotiating clinical trial contracts and budgets between biopharmaceutical companies, contract research organizations and investigator sites around the world

executing and tracking payments from the research sponsor to its associated research sites for payment for research studies; developing global budgets that align with payment processes with ongoing analysis of negotiated budgets

providing safety and ethics instruction in the field of scientific clinical trials to the officials within the research site who oversee the human subjects during research

providing a web site featuring technology enabling others to manage and exchange healthcare research information; providing use of non-downloadable computer software via the internet for managing healthcare research and support information; providing consultation in the development and maintenance of standards required to meet accreditation by others in the field of clinical trials involving human subjects and research protocols relating to same; scientific writing and editing of research protocols for others involved in human subjects research; developing research protocols for others involved in human subjects research; providing scientific review of human subjects research protocols as to the merit, design and risks involved; providing services in support of clinical trial start-up and management, namely, developing and managing a web-accessed technology platform used for facilitating communication between clinical trial sponsors, contract research organizations, and clinical trial sites; providing a website featuring technology that enables users to collect, manage and share documents to facilitate communication during clinical trials; conducting assessment surveys regarding suitability for site participation in clinical trials and utilizing data analytics to select appropriate clinical trial site locations; providing online non-downloadable software for posting, tracking, and accessing reports related to clinical training courses attended by clinical trial clinicians; providing scientific research related information services to prospective or current clinical trial participants to increase engagement and retention in clinical trials via telephone and email; providing scientific research related information services to prospective or current clinical trial participants for clinical assistance and quality assurance purposes to increase rater reliability in trials where subjective scales are relied upon to improve rating consistency and trial efficacy

providing an on-line database featuring healthcare research information

providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; providing consultation to develop a corrective action plan for research misconduct or issues of noncompliance; offering a variety of global contract negotiation resource placement, supported by technology-driven processes and a network of international attorneys who possess specialized, in-depth knowledge of local languages and regulations