aktaPD®’s senior CRAs work closely with sites to identify potential risks associated with set-up, enrollment, quality, and management of all clinical activities. Our team’s goal is clear: better, collaborative decision-making on site selection and subject/investigator engagement efforts resulting in optimal trial execution that is cost- and time-effective, compliant, and with a solid contingency plan to manage and mitigate risk.

Our team expertly employs a variety of metrics and tools to ensure site—and, ultimately—trial success:

  • Disease prevalence/incidence
  • History of SAEs
  • Technology infrastructure/access
  • Illustration of subject availability
  • Number of competing trials (for both subjects and site resources analysis)
  • Recruitment potential based on published trial rates
  • Site staff retention ratio
  • Budget management (with less than 10% request for change order)

Need support in writing and managing global study protocols that work? Contact us.




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