Profound Research
Profound Research is dedicated to advancing medicine through innovative clinical trials, connecting sponsors with top investigators and patient populations to ensure fast, high-quality research. Their mission is to improve lives by providing advanced therapeutic options, with a vision to create the best patient-physician experience in clinical research. They emphasize core values of compassion, urgency, solution orientation, and excellence, and operate with a strong commitment to ethical standards, regulatory compliance, and patient-centered care.
Industries
Nr. of Employees
small (1-50)
Profound Research
Nashville, Tennessee, United States, North America
Services
End-to-end site management including staffing, protocol execution, monitoring, and local site logistics.
Accelerated contracting, budgeting, regulatory coordination and site activation to shorten time-to-first-patient-in.
Recruitment leveraging physician partnerships and a centralized patient database to identify and enroll eligible participants.
Full administrative and regulatory support including IRB coordination, compliance oversight, and study logistics.
Model to integrate clinical trials into physician practices with minimal workflow disruption and dedicated research coordinators.
Protocol feasibility assessments, site qualification, and selection to match study requirements with site capabilities and patient populations.
End-to-end site management including staffing, protocol execution, monitoring, and local site logistics.
Accelerated contracting, budgeting, regulatory coordination and site activation to shorten time-to-first-patient-in.
Recruitment leveraging physician partnerships and a centralized patient database to identify and enroll eligible participants.
Full administrative and regulatory support including IRB coordination, compliance oversight, and study logistics.
Model to integrate clinical trials into physician practices with minimal workflow disruption and dedicated research coordinators.
Protocol feasibility assessments, site qualification, and selection to match study requirements with site capabilities and patient populations.
Expertise Areas
- Clinical trial management
- Site network operations and practice-integrated research
- Patient recruitment and retention
- Study startup and rapid activation
Key Technologies
- Centralized patient registry
- Electronic data capture (EDC) and clinical trial management systems (CTMS)
- Clinical data reporting and analytics
- EHR integration (inferred)