Clinical Monitoring

We believe that professional clinical research associates (CRAs) form the backbone of any successful research study. At Theorem Clinical Research, our dedicated team of CRAs — many with diverse clinical backgrounds including MDs, RNs, scientists and clinical specialists — maintain a focus on three vital aspects of a successful trial:

• Qualifying the right investigators for each trial
• Training and supporting investigator site staff, and
• Ensuring patient safety and data integrity

 

PROFESSIONAL EXPERIENCE

Theorem CRAs have effectively monitored biopharmaceutical and medical device studies across all phases of product development and ensure ICH/GCP compliance and data integrity at each site visit. CRAs and other team members, most with more than five years of field experience are chosen to be a part of your study based in part on their experience in your therapeutic area of interest. This customized approach ensures a detail-oriented team that can minimize start-up time and help ensure smooth, successful trials from start to finish.

ONGOING TRAINING

As part of our commitment to quality monitoring services, we provide our CRAs with a comprehensive training and professional development program to help ensure compliance with applicable laws, regulations and guidelines around the world.

GLOBAL PRESENCE

Theorem 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 throughout North and South America, Europe, the Middle East and the Asia-Pacific Rim.