Total Diversity Clinical Trial Management
TOTAL Diversity Clinical Trial Management is a full-service clinical research organization dedicated to delivering personalized, efficient, and high-quality clinical trial solutions. With a focus on diversity, community engagement, and regulatory expertise, they aim to optimize patient enrollment, ensure regulatory compliance, and foster inclusive research practices. Their innovative tools like DTEACH and D DASH support diverse recruitment and data monitoring, making them a trusted partner for biotech, pharma, and medical device companies seeking a flexible and client-centric CRO experience. They also emphasize patient engagement and protocol flexibility to improve participation and retention in clinical trials.
Industries
Nr. of Employees
small (1-50)
Total Diversity Clinical Trial Management
Dallas, Texas, United States, North America
Products
Diversity enrollment metrics dashboard
Dashboard that integrates live enrollment feeds from EDC or IWRS to report participant demographics and progress against preset diversity goals.
Self-paced diversity training platform for clinical sites
Online training portal providing evidence-based modules and best practices to improve site-level diversity planning and execution.
Site diversity assessment and benchmarking tool
Structured assessment instrument that evaluates sites on diversity and inclusion criteria and produces a numerical benchmark to guide site selection and improvement plans.
Study-specific patient-facing website package
Design, hosting and content for patient-facing websites including site locator, FAQs, regulatory-aligned pre-screeners and contact mechanisms to support recruitment.
Diversity enrollment metrics dashboard
Dashboard that integrates live enrollment feeds from EDC or IWRS to report participant demographics and progress against preset diversity goals.
Self-paced diversity training platform for clinical sites
Online training portal providing evidence-based modules and best practices to improve site-level diversity planning and execution.
Site diversity assessment and benchmarking tool
Structured assessment instrument that evaluates sites on diversity and inclusion criteria and produces a numerical benchmark to guide site selection and improvement plans.
Study-specific patient-facing website package
Design, hosting and content for patient-facing websites including site locator, FAQs, regulatory-aligned pre-screeners and contact mechanisms to support recruitment.
Services
End-to-end clinical trial services including study startup, project management, monitoring, site support, and close-out for drug, biologic, and device studies.
Project kick-off, feasibility assessments, site identification and access, and protocol-aligned site activation planning informed by diversity-focused site benchmarking.
Design and implement recruitment campaigns, community outreach, physician referral programs, recruitment kits and site visits to meet demographic enrollment targets.
CDM services including EDC support, automated edit checks, discrepancy management, source data verification guidance, secure data storage and regulatory-ready reporting.
Advisory services for regulatory planning, global standards alignment and preparation for interactions with regulatory authorities.
Self-paced, evidence-based training for site teams focused on diversity, equity, and inclusion best practices and operational changes to improve diverse enrollment.
End-to-end clinical trial services including study startup, project management, monitoring, site support, and close-out for drug, biologic, and device studies.
Project kick-off, feasibility assessments, site identification and access, and protocol-aligned site activation planning informed by diversity-focused site benchmarking.
Design and implement recruitment campaigns, community outreach, physician referral programs, recruitment kits and site visits to meet demographic enrollment targets.
CDM services including EDC support, automated edit checks, discrepancy management, source data verification guidance, secure data storage and regulatory-ready reporting.
Advisory services for regulatory planning, global standards alignment and preparation for interactions with regulatory authorities.
Self-paced, evidence-based training for site teams focused on diversity, equity, and inclusion best practices and operational changes to improve diverse enrollment.
Expertise Areas
- Clinical trial management and operations
- Site feasibility and diversity benchmarking
- Diverse patient recruitment and retention
- Clinical data management and data quality
Key Technologies
- Electronic data capture (EDC)
- Interactive randomization and drug supply systems (IWRS/IVRS)
- Real-time enrollment and diversity dashboards
- Mobile health applications
News & Updates
Recognition of outstanding team member contributions at TOTAL Diversity.
Leadership recognition for advancing diversity, equity, and inclusion in clinical trials on a global scale.
Highlighting top boutique CROs including TOTAL Diversity, emphasizing their strengths in personalized support and diversity initiatives.
Overview of leading CROs including TOTAL Diversity, ICON, Parexel, Medpace, and Syneos Health.
CROs play a key role in drug development, helping pharmaceutical and biotech firms run clinical trials and bring medicines to market faster.
Clinical data management involves collecting, cleaning, and managing data from trials to ensure accuracy and reliability, supported by systems like CDM.
Recognition of outstanding team member contributions at TOTAL Diversity.
Leadership recognition for advancing diversity, equity, and inclusion in clinical trials on a global scale.
Highlighting top boutique CROs including TOTAL Diversity, emphasizing their strengths in personalized support and diversity initiatives.
Overview of leading CROs including TOTAL Diversity, ICON, Parexel, Medpace, and Syneos Health.
CROs play a key role in drug development, helping pharmaceutical and biotech firms run clinical trials and bring medicines to market faster.
Clinical data management involves collecting, cleaning, and managing data from trials to ensure accuracy and reliability, supported by systems like CDM.