Clinical Services > Clinical Trial Project Management
The PRC Clinical Project Manager is the team leader and serves as the Sponsor liaison and works to create the best suited team for each clinical program
Our project managers are extremely customer focused and directly accountable to Sponsor for all project-related responsibilities which, among others, include team coordination and training, investigator and subject recruitment, communications with sites and sponsor, project tracking and on-time reporting as well as meeting project timelines.
The Clinical Trial Project Manager manages all activities coordinated thorough study team meetings and communications, including study start-up activities, maintenance to study close-outs by utilizing our proprietary CTMS to report up-to-date study status, patient enrollment, site information and deadline and milestone tracking for regulatory documents and submissions.
Key advantages to partnering with PRC Clinical for Clinical Trial Project Management include:
- Full SOPs (Standard Operating Procedures)
- Study & site startup activities
- Documents and Submissions
- IRB/EC meeting activity
- Contracts & budgets
- Screening and enrollment
- Study subject activity throughout the trial
- Regulatory documents (electronic and hard-copy)
- Monitoring visit Reports, calendars and schedules
- Safety Reporting
- And much more!