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Clinical Trial Design

Develop study-related protocols, case report forms (CRFs) and database tools for records management.
Quality Control

Ensure products or services adhere to a set minimum standard.
Publication Writing

Make clear and accurate presentations of scientific and technical data.
Clinical Protocol Design & Development

Creation of clinical protocol document which details how a clinical trial is designed, relating to to the methodology, hypothesis, and operation of clinical trial to ensure the safety of the patients is maintained as well as maintaining the integrity of the data collected during the trial.
Site Monitoring

Maintain oversight over participant's health during a clinical trial.
Patient Recruitment

Recruit and retain patients for clinical trials.
Biostatistical Design

Use statistics to ensure appropriate pre-clinical and clinical study design.
Site Selection

Select clinical trial sites with clinicians who recruit, enroll, treat and evaluate trial patients.
Observational Research

Research method for documenting clinical, economic, and or humanistic outcomes of actual medical practice absent the constraints of a more formal experimental design. See also Pragmatic Clinical Trials.
Case Report Monitoring & Auditing

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