About Clinical Research Path

Our Mission

To support research excellence through reliable coordination, accurate documentation, and analytical expertise—helping sites and investigators achieve high-quality outcomes efficiently.

Areas of Service

1. Clinical Research Staffing

• Provide qualified Clinical Research Coordinators (CRCs) and Clinical Research Assistants (CRAs) for on-site or remote study support.

• Offer flexible, project-based coordination tailored to each study’s specific needs.

2. CRC Qualification and Training

• Train and qualify future clinical research coordinators through hands-on learning in study coordination, documentation, and site management.

• Develop a skilled research workforce ready to support clinical trials effectively.

3. Investigator Identification and Support

• Assist in navigating and selecting potential Principal Investigators (PIs) for upcoming research projects.

• Facilitate the collection of site feasibility information and investigator documentation.

4. Documentation and Site File Management

• Organize and maintain site essential documents, investigator CVs, licenses, and study logs.

• Set up and manage the Trial Master File (TMF) and Investigator Site File (ISF) in compliance with study requirements.

5. Research Writing and Data Services

• Develop study proposals, reports, and patient brochures.

• Provide clinical research data analysis and biostatistics services, including data interpretation and statistical summaries.