Services & Experts

Consultation experts offer advice and assistance in these key areas. Please check back frequently as additional services will continue to be added. 

Service Experts Areas
Biostatistics (Data Management/Analysis)
  • Data management systems that are flexible enough to allow study-specific modules, but complete enough for consistency across studies (such as RedCap), but augmented for FDA auditable trials and which include (but are not limited to) modules to support logistical operations including recruitment, eligibility tracking, patient scheduling, randomization, data entry and validation, QA/QC, study progress tracking, adverse event reporting and tracking, drug distribution and accountability, and design or advise on standard reports and study specific progress reports.

  • Analysis of pooled data across the multiple studies facilitated by REACT, for both scientific contributions to the literature as well as future study planning.
Clinical Trials Design/Implementation
  • Statistical expertise and support for the development or refinement of the study question with the requisite protocols and for the analysis of study data.

  • Careful conceptualization, advice in planning, and implementation for each phase of the investigator’s proposed studies including design, statistical, logistical advice in general, and study specific SOPs and Manuals of Procedures (MOPs), study protocols, CRFs, and consent/assent forms.
Epidemiology
  • Statistical expertise and support for the development or refinement of the study question with the requisite protocols and for the analysis of study data.

  • Incorporation of mechanistic secondary outcomes as appropriate, and provide access to a comprehensive menu of REACT core facilities to complete these ancillary experiments at the REACT, or training to do so at the investigator’s home institution or another P2C resource center.

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