Clinical Development Programs
Clinical Project Management
MVG Project Managers are extremely customer-focused and directly accountable to the 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.
Key advantages to partnering with MVG Consulting for Clinical 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
![mvgclinicalresearchmanagementclinicalprojectmanagement | MVG Consulting Services mvg clinical research management clinical project management](https://nisse.serpcom.com/mvg/wp-content/uploads/sites/4/2017/12/mvg-clinical-research-management-clinical-project-management.jpg)