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To better assist you with your request, please choose a research area provided by Christine Towey Consulting. In case you cannot find an exact match, simply select any service, and our concierge team will swiftly address it once your request has been submitted.

Site Monitoring

Maintain oversight over participant's health during a clinical trial.
Site Selection

Select clinical trial sites with clinicians who recruit, enroll, treat and evaluate trial patients.
Case Report Monitoring & Auditing

Ensure the adequate collection and traceability of clinical data in preparation for review by the FDA.
Study/Site Feasibility Study

Explore and test study practicality.
Investigator Meeting Planning & Execution

Investigator planning and meetings ensure that there is proper communication and reliability during a clinical trial. Allows for efficient work flow.
Site/Patient Payments

Allow for different suppliers to organize the proper patient and site payments for a clinical trial. Provides real-time payments, reduce workloads for site staff and minimize the amount of time participants spend waiting to be paid.