Thorough clinical trial monitoring ensures study integrity, protocol adherence, patient safety, and accurate data collection. Our experienced Clinical Research Associates (CRAs) are therapeutically aligned and centrally trained. In fact, to ensure consistent study execution, we conduct rigorous, ongoing in-house training programs for all employees.

DP Clinical’s CRAs have been with us, on average, 5+ years, and our attrition rate is less than 10% – meaning you won’t have to worry about team turnover – an important consideration when selecting a CRO partner.

DP Clinical’s CRAs hold RN, BS, or MS degrees in a scientific discipline, have diverse language skills, and are located throughout the US. Through our affiliates around the world, DP Clinical can also meet monitoring needs globally. Our geographic reach allows us to provide high-quality, cost-effective monitoring for clinical trials no matter where the sites or patients are located.

DP Clinical’s monitoring services include:

  • Study procedures development
  • Onsite and remote clinical monitoring
  • Risk-based monitoring
  • Source document review
  • Patient eligibility and compliance tracking
  • IP management
  • Adverse event reporting and follow up
  • Regulatory compliance monitoring and documentation maintenance