At SCRI we aim to provide effective, efficient high quality single and multisite project management for all SCRI projects and clinical sites.

SCRI provides Project Management expertise and support including:

• Assist Investigators in preparing protocols that are based on project proposals
• Assist Investigators in designing informed consent template (in English) based on study protocol
• Develop project specific work processes and guidelines (that meet regulatory requirements as appropriate) for each protocol to ensure smooth operations of the project and enhance project quality and efficiency
• Provide and coordinate the multiple steps and elements needed for efficient protocol implementation
• Develop project specific materials and tools to assist Principal Investigators (PIs) and site personnel with carrying out the project
• Identify and troubleshoot clinical and research procedures for each project
• Collaborate and function as Project Managers/Project Leaders as appropriate
• Recommend research to enhance recruitment, retention and treatment adherence for all projects

The Project Management expertise is offered as part of SCRI’s Research Operations Division. To learn more about SCRI’s Research Operations, please click here.

To engage SCRI’s Project Management expertise, please click here if you are planning an Investigator initiated study, or click here for other studies.