[Class : 35] Clinical Research Site Management And Monitoring, Namely, Identifying, Qualifying, And Selecting Sites For Clinical Trials, Negotiating Clinical Trial Site Contracts And Budgets, Organizing And Conducting Business Meetings Of Clinical Trial Investigators, Assisting Investigators With Developing Business Strategies For Recruiting Clinical Trial Participants, Submitting Clinical Trial Protocols To Institutional Review Boards And Independent Ethics Committees, Monitoring Clinical Trial Investigators' Activities For Compliance With Clinical Protocols And Regulations And For Patient Safety; Employment Staffing In The Field Of Clinical Trials; Business Information Management.