ProTrials Research
ProTrials Research, Inc. is a full-service clinical research organization (CRO) dedicated to delivering high-quality clinical research services across various therapeutic areas. With a focus on excellence, collaboration, integrity, community, and balance, ProTrials supports the pharmaceutical, biotechnology, and medical device industries with site management, clinical monitoring, project management, data management, and supportive clinical development services. Since 1996, it has completed over 775 projects at more than 17,500 sites involving over 210,000 subjects, emphasizing innovation and patient health worldwide.
Industries
Nr. of Employees
medium (51-250)
ProTrials Research
Products
Virtual Trials Data Sheet (PDF)
Datasheet describing the company's approach to incorporating decentralized study management techniques and related technologies for reduced site burden and remote monitoring.
Zelta™ EDC
Innovative electronic data capture platform enhancing data management capabilities for clinical trials.
IBM Clinical Development
A cloud-based, unified platform used by ProTrials Research, Inc. to improve data management services and facilitate audits by creating accurate digital records of clinical study actions.
Fully Virtual Trials
A fully virtual clinical trial solution where all trial activities are conducted remotely, focusing on patient-centric approaches including telemedicine, eConsent, eDC, and direct shipment of drugs/devices to patients.
Hybrid Trials
A hybrid clinical trial solution where selected trial activities are conducted virtually, replacing some in-clinic visits with remote visits using the same virtual technology and processes.
Remote Monitoring Strategy
A blended remote monitoring strategy to supplement on-site monitor visits, providing real-time monitoring, proactive data cleaning, and efficiencies through reduced travel.
Virtual Trials Data Sheet (PDF)
Datasheet describing the company's approach to incorporating decentralized study management techniques and related technologies for reduced site burden and remote monitoring.
Zelta™ EDC
Innovative electronic data capture platform enhancing data management capabilities for clinical trials.
IBM Clinical Development
A cloud-based, unified platform used by ProTrials Research, Inc. to improve data management services and facilitate audits by creating accurate digital records of clinical study actions.
Fully Virtual Trials
A fully virtual clinical trial solution where all trial activities are conducted remotely, focusing on patient-centric approaches including telemedicine, eConsent, eDC, and direct shipment of drugs/devices to patients.
Hybrid Trials
A hybrid clinical trial solution where selected trial activities are conducted virtually, replacing some in-clinic visits with remote visits using the same virtual technology and processes.
Remote Monitoring Strategy
A blended remote monitoring strategy to supplement on-site monitor visits, providing real-time monitoring, proactive data cleaning, and efficiencies through reduced travel.
Services
Comprehensive clinical research services spanning project management, site management, clinical monitoring, data management, and regulatory support for studies across phases I–IV.
Project and program management for planning, tracking, and delivery of clinical study milestones.
Operational support for trial conduct including site oversight, monitoring, and participant safety operations.
Data management services including EDC integration, database setup, and generation of audit-ready datasets.
Quality systems and audit preparation to support compliance and inspection readiness at site and program levels.
Medical oversight and regulatory support to assist with regulatory documentation, interactions, and medical review activities.
Comprehensive clinical research services spanning project management, site management, clinical monitoring, data management, and regulatory support for studies across phases I–IV.
Project and program management for planning, tracking, and delivery of clinical study milestones.
Operational support for trial conduct including site oversight, monitoring, and participant safety operations.
Data management services including EDC integration, database setup, and generation of audit-ready datasets.
Quality systems and audit preparation to support compliance and inspection readiness at site and program levels.
Medical oversight and regulatory support to assist with regulatory documentation, interactions, and medical review activities.
Expertise Areas
- Clinical trial management
- Clinical monitoring and site management
- Clinical data management
- Regulatory support and quality assurance
Key Technologies
- Electronic Data Capture (EDC) integration
- Decentralized trial platforms
- Remote monitoring platforms
- Clinical trial management systems (CTMS)
News & Updates
Top 2,500 companies identified by Inc. Magazine’s Inc. 5000.
Founders & Co-CEOs both voted PharmaVOICE 100 Most Inspiring Leaders in Life Sciences.
Top 2,500 companies identified by Inc. Magazine’s Inc. 5000.
Founders & Co-CEOs both voted PharmaVOICE 100 Most Inspiring Leaders in Life Sciences.