Project management
UCR provides project management for clinical studies, from planning and start-up to conduct and reporting.
We ensure structure, progress and coordination throughout the project, in line with applicable regulations
How we can support you
- Act as the main point of contact for sponsorsTake overall responsibility for project planning, including timelines, budget and resources
- study protocols
- patient information and informed consent
- clinical study reports (CSRs)
- manuals and instructions
- Conduct risk assessments and implement structured risk management
- Manage contracts with sponsors, sites and vendors
- Prepare and coordinate key study documentation, such as:
- Lead and coordinate the study team in a cross-functional set-up
Contact us
Need support with project management for your study? Get in touch to learn more.