Tranquil Clinical Research
Clinical research organization focused on early‑phase and full‑service CRO support, including a hospital‑based Phase I unit. Services span study start‑up through closeout, sponsor oversight/CRO oversight, data management, regulatory support, pharmacovigilance, and patient recruitment. Operates a Functional Service Provider model for CRA staffing, training and monitoring support.
Industries
Nr. of Employees
medium (51-250)
Tranquil Clinical Research
Webster, Texas, United States, North America
Products
Full-Service CRO
Provides comprehensive clinical research organization services managing clinical trial operations from study startup to closeout.
Phase I Unit Services
Hospital-based clinical trial services focused on early-phase, first-in-human studies.
Triumph Functional Service Provider (FSP)
Delivers functional service provider solutions including clinical research associate staffing and oversight for clinical trials.
Clinical Trial Monitoring
Monitors clinical trial conduct to ensure compliance with protocols and regulatory requirements.
Study Start-up Services
Manages the initiation phase of clinical trials including regulatory submissions and site activation.
Study Rescue Services
Intervenes in troubled clinical trials to address issues and bring studies back on track.
Full-Service CRO
Provides comprehensive clinical research organization services managing clinical trial operations from study startup to closeout.
Phase I Unit Services
Hospital-based clinical trial services focused on early-phase, first-in-human studies.
Triumph Functional Service Provider (FSP)
Delivers functional service provider solutions including clinical research associate staffing and oversight for clinical trials.
Clinical Trial Monitoring
Monitors clinical trial conduct to ensure compliance with protocols and regulatory requirements.
Study Start-up Services
Manages the initiation phase of clinical trials including regulatory submissions and site activation.
Study Rescue Services
Intervenes in troubled clinical trials to address issues and bring studies back on track.
Services
Clinical trial monitoring
Monitoring services delivered on‑site, remote, centralized or decentralized to oversee protocol adherence and data integrity.
Data management & electronic data capture
Complete data management services including EDC to support study dataset capture and quality.
Medical monitoring and pharmacovigilance
Clinical safety oversight and pharmacovigilance services to monitor and report adverse events.
Pre‑clinical phase support
Services to support pre‑clinical stage activities and prepare programs for clinical transition.
Project management
Full clinical project management covering planning, execution, and oversight.
Regulatory affairs
Support for global regulatory law interpretation, filings and agency interactions.
Clinical trial monitoring
Monitoring services delivered on‑site, remote, centralized or decentralized to oversee protocol adherence and data integrity.
Data management & electronic data capture
Complete data management services including EDC to support study dataset capture and quality.
Medical monitoring and pharmacovigilance
Clinical safety oversight and pharmacovigilance services to monitor and report adverse events.
Pre‑clinical phase support
Services to support pre‑clinical stage activities and prepare programs for clinical transition.
Project management
Full clinical project management covering planning, execution, and oversight.
Regulatory affairs
Support for global regulatory law interpretation, filings and agency interactions.
Expertise Areas
- Clinical trial management
- Early‑phase / Phase I unit operations
- Sponsor oversight and CRO governance
- Patient recruitment and retention
Key Technologies
- Electronic data capture (EDC) systems
- Remote monitoring and decentralized trial methods
- Clinical trial metrics and QC reporting
- Protocol development and regulatory submission workflows