The S.P.E.E.D. Advantage

---

Our approach is shaped by experience across multiple sides of clinical research, providing a broader understanding of what sites need to perform successfully.

• Site Perspective
  • Understand the day-to-day realities of executing clinical trials, supporting patients, managing documentation, and meeting study requirements.
• CRO & FSP Perspective
  • Understand monitoring expectations, site performance oversight, escalation pathways, and operational delivery.
• Sponsor Perspective
  • Understand what pharmaceutical and biotechnology organizations expect from qualified, reliable, high-performing research sites.
• Leadership Perspective
  • Bring experience in global clinical operations, quality, risk management, team development, and trial delivery.

Identifying a problem is only the beginning. We look beyond the finding to understand why it happened and what the site needs to prevent it from happening again.

• Identify the Gap
  • Determine where performance, knowledge, process, or compliance issues exist.
• Understand the Root Cause
  • Evaluate the people, processes, systems, and operational conditions contributing to the issue.
• Build the Solution
  • Develop practical corrective actions, training, workflows, or process improvements.
• Strengthen the Team
  • Give site personnel the knowledge and tools needed to implement change successfully.
• Sustain the Improvement
  • Establish practices that help prevent recurring issues and support long-term performance.

Clinical research training should do more than check a box. We focus on helping site teams understand how requirements translate into everyday trial execution.

• Practical
  • Training connects regulatory and protocol requirements to real-world site responsibilities.
• Role-Specific
  • Content can be tailored for coordinators, investigators, research managers, regulatory personnel, and other site professionals.
• Site-Specific
  • Training can address the actual operational challenges, findings, or knowledge gaps affecting your site.
• Action-Oriented
  • Teams leave with a clearer understanding of what to do, why it matters, and how to apply it consistently.
• Flexible
  • Training can be delivered virtually or onsite based on site needs.

Technology Partnership with Medidata

Through our partnership with Medidata, Divergent S.P.E.E.D. connects clinical research expertise with technology solutions that support efficient, high-quality trial execution.

• Electronic Data Capture (EDC) Support
  • Support effective data collection, review, and site workflows.
• Clinical Trial Management System (CTMS) Support
  • Strengthen study tracking, operational visibility, and trial management processes.
• eCOA & eConsent Solutions
  • Support digital patient engagement, clinical outcome assessments, and informed consent processes.
• Study Build & Implementation Support
  • Help translate study requirements into practical technology-enabled workflows.
• Data Review & Workflow Optimization
  • Strengthen processes that support timely, accurate, and high-quality clinical trial data.
• Site Technology Readiness
  • Help research teams understand and prepare for the technology requirements involved in modern clinical trial execution.

Our approach turns site challenges into structured, actionable solutions.

• Strategy
  • Understand the challenge, site environment, priorities, and desired outcome.
• Precision
  • Identify the specific gaps, risks, processes, and behaviors affecting performance.
• Excellence
  • Establish clear standards for quality, compliance, and operational execution.
• Execution
  • Put solutions into practice through training, workflows, tools, and targeted support.
• Delivery
  • Help teams sustain improvements and consistently deliver high-quality clinical research.

No Two Research Sites Are the Same

Every research site has unique needs, challenges, and opportunities. Our support is tailored to the realities of your site—not a one-size-fits-all approach.

• Your Team
  • Support tailored to your investigators, coordinators, research managers, and staff.
• Your Studies
  • Solutions aligned with your protocols, therapeutic areas, and clinical trial portfolio.
• Your Operations
  • Support designed around your systems, workflows, staffing model, and operational environment.
• Your Challenges
  • Targeted solutions for training gaps, performance concerns, inspection readiness, site rescue, and other site-specific needs.
• Your Path Forward
  • We meet your site where it is today and help build the capabilities needed for stronger performance tomorrow.