Experience the Clinical Trial Workflow Through Their Eyes
Meet the people behind the process. See their challenges. Watch how AI and automation transform their daily work.
Trusted by 500+ Clinical Research Teams
1
Sarah Johnson
Trial Manager
“Managing multiple studies was overwhelming until SourceDox brought everything into one intelligent dashboard.”
70% Time Savings
12 hours/week with 70% automation
Their Challenges, Our Solutions
Every role in clinical trials faces unique obstacles. See how SourceDox transforms their daily experience.
Sarah Johnson
Trial Manager
“Managing multiple studies was overwhelming until SourceDox brought everything into one intelligent dashboard.”
CHALLENGES
- Juggling multiple studies across different systems
- Manual enrollment tracking and projections
- Delayed risk identification and mitigation
- Time-consuming site performance reviews
- Fragmented communication with stakeholders
SOLUTIONS
- Unified multi-study oversight dashboard
- AI-powered enrollment predictions
- Automated risk alerts and mitigation suggestions
- Real-time site performance analytics
- Integrated communication and reporting tools
70% Time Savings
12 hours/week with 70% automation
Michael Chen
Data Manager
“Data quality issues that used to take weeks to resolve now get flagged and fixed in real-time.”
CHALLENGES
- Manual data validation across multiple EDCs
- Query resolution bottlenecks
- Inconsistent data quality metrics
- Time-intensive database lock processes
- Delayed discrepancy identification
SOLUTIONS
- Automated data validation rules
- Intelligent query management system
- Real-time quality dashboards
- Streamlined database operations
- Predictive discrepancy detection
92% Query Efficiency
98% data quality with same-day resolution
Lisa Rodriguez
Study Coordinator
“My site team can now focus on patient care instead of drowning in paperwork and scheduling conflicts.”
CHALLENGES
- Complex subject scheduling coordination
- Manual CRF completion and tracking
- Protocol deviation management
- Regulatory compliance monitoring
- Staff training and certification tracking
SOLUTIONS
- Intelligent visit scheduling system
- Streamlined eCRF workflows
- Automated deviation tracking
- Built-in compliance monitoring
- Centralized staff management portal
48% Better Enrollment
12% screen failure rate, 28-day enrollment
James Wilson
Clinical Research Associate
“Remote monitoring capabilities have revolutionized how I ensure site compliance and data integrity.”
CHALLENGES
- Time-consuming on-site monitoring visits
- Manual compliance tracking
- Delayed deviation identification
- Paper-based monitoring reports
- Inconsistent site performance metrics
SOLUTIONS
- Risk-based remote monitoring tools
- Automated compliance scoring
- Real-time deviation alerts
- Digital monitoring reports
- Standardized site performance dashboards
60% Travel Reduction
40% on-site visits, same-day reporting
By The Numbers
Quantified impact across every persona in your clinical trials
Time Savings
Average reduction in administrative tasks across all personas
Data Quality
Improved data accuracy with automated validation systems
Faster Enrollment
Accelerated patient recruitment through AI optimization
Cost Savings
Average annual savings per study through efficiency gains
Ready to Transform Your Trials?
Experience the difference that AI-powered clinical trial management can make for your team
Trusted by 500+ Clinical Research Teams