Clinical Trial Preparation Phase
- Provide full-time or part-time, professional and experienced trial personnel
- Effectively facilitate communication between pharmaceutical companies and trial sites
- Plan subject enrollment strategies and directions based on study characteristics to shorten enrollment time
- Assist in communication with Institutional Review Boards (IRBs) and research institutions
- Facilitate communication among various trial-related departments
- Assist in establishing standard operating procedures for trial sites
- Assist in arranging and participating in relevant meetings
- Assist in collecting submission documents and tracking submission progress