Efficient, Effective Phase I-III Study Management


At Clinipace, our goal is to help you get your new therapeutic to market as quickly as possible while maintaining your milestones. With us, you get a dedicated and transparent team. Our project managers coordinate all aspects of your study, and our medical, regulatory and operational experts are ready to execute your program and get you answers. Not only is our team dedicated to delivering the most efficient and safe clinical research, we help you thoroughly understand the safety, efficacy and side effects of your investigational new drug or device to ensure the success of your trial.


  • Biostatistics and statistical programming
  • Clinical analytics
  • Clinical data management
  • Clinical operations
  • Clinical technology
  • Investigator recruitment and site selection
  • Medical monitoring
  • Medical writing
  • Project management
  • Quality assurance
  • Regulatory affairs
  • Safety/pharmacovigilance