Our Services
We offer support for developing clinical trials from start to finish. This includes helping design the study, preparing the necessary documents, coordinating with research teams, site monitoring, and data analysis. We also assist with protocol writing, regulatory strategy guidance, and ensuring data collection methods support integrity and reproducibility. We help lay a strong foundation for trials by aligning study objectives with ethical standards and regulatory expectations.
BIOSTATISTICS
•Study design, including traditional, adaptive and Bayesian design
•Statistical analysis plan development
•Statistical Reporting
•Interim and final analyses
•Metrics
•Data Sharing
DATA QUALITY
•Data collection design
•Data merging and data cleaning
•Data science and analytics
•Public use data sets
INFORMATION TECHNOLOGY
•Software development
•Application and website maintenance
•Database management
•Web server oversight
CLINICAL OPERATIONS AND COMPLIANCE
•Project management
•Quality management
•Regulatory compliance
•Safety management
RESEARCH ADMINISTRATION
•Grant development and budgeting
•Diverse communication strategies
•Meeting planning and support
•Fiscal administration
•Quality assurance
INTERESTED IN A CONSULT?
If you would like to set up a consult to discuss your project and how the CTSDMC may be able to help you, contact us by following the link.