Product/Service

Global Clinical Monitoring

Source: Theorem Clinical Research
At Theorem Clinical Research, we have a global team of Clinical Research Associates (CRAs) who are focused on three primary objectives: qualifying the right physicians for the trial; initial and ongoing training and support of Investigator site staff; and ensuring the study is met with the highest standard of patient safety and data integrity.

At Theorem Clinical Research, we have a global team of Clinical Research Associates (CRAs) who are focused on three primary objectives: qualifying the right physicians for the trial; initial and ongoing training and support of Investigator site staff; and ensuring the study is met with the highest standard of patient safety and data integrity.

Our CRA professionals have effectively monitored studies across all phases of product development and ensure ICH/GCP compliance and data integrity at each site visit -- consistently collecting high-quality clinical data on-time.

We strive for excellence by placing great emphasis on management, support, recognition, training, accountability and personal development. By providing our monitoring professionals with these value-added tools, we're not only contributing to strong project outcomes -- we're also exceeding your expectations through exceptional service.

  • Experienced Professionals. Our people average five years of field monitoring experience and in a variety of therapeutic areas. They are highly educated professionals with diverse clinical backgrounds, including M.D.s, R.N.s, scientists and clinical specialists. Our CRA retention rate is excellent due to high job satisfaction.
  • Customized Teams. Every CRA becomes a part of your project team, which is structured to meet your individual needs, and focus in particular on therapeutic expertise and geographic scope. This customized approach produces an experienced, detail-oriented team who excels with minimal start-up time and consistently provides superior monitoring services throughout the duration of the project.
  • Proactive Management Structure. We've structured ourselves to offer our CRAs unparalleled support and strong leadership. Each CRA reports directly to an experienced Clinical Monitoring Manager who strives to engage and support CRAs, while also conducting hands-on training and evaluation in the field. Our managers have an average of approximately 20 years of experience.
  • Comprehensive Training and Development. As part of our ongoing commitment to ensuring you receive quality monitoring services, we provide our CRAs with a comprehensive training and development program. Our established mentoring programs support both in-house CRAs and those located regionally, helping to ensure compliance with applicable laws, regulations, and guidelines around the world.
  • Global Presence. Our CRAs are located around the globe. Many CRAs are regionally based to maximize on-site time and lower travel costs. Our global systems, tools, and processes provide the support necessary to create efficiencies in the field. We currently have staff in North and South America, Europe, Africa, and the Asia Pacific Rim.