2. The Contractor shall perform activities related with overall administration and implementation of the site-specific clinical operation services and perform protocol reviews and provide ad-hoc consultation. Activities may include, but are not limited to, the setup for overall site-specific project management plans, protocol reviews and adhoc consultation for anticipated clinical studies, meeting participation, preparation, and submission of regulatory and information security related deliverables (information security requirements/deliverables take effect upon the award of a Clinical Trial Execution Task Order under IDIQ Performance Area B) and the ongoing archival of completed trial data and reports.