Phase II & III Experience


InFocus Clinical Project Managers, Clinical Research Monitors and administration have worked for and with sponsor companies and CROs large and small, offering a unique and invaluable experience and insight. Clinical Research Professionals bring their unique and tremendous experience to InFocus Clinical because or our commitment to and reputation of offering the highest quality clinical research services.


experience two Phase II and III studies require a different level of expertise due to the length, complexity in design, and knowledge of the diverse indications. InFocus Clinical Research is able to provide you with the confidence and reassurance that our wide range of clinical trial experience and services are able to conquer the myriad issues faced in research today. Our experienced, therapeutically aligned staff ensure:

  • Site and investigator selection are done with the best interest of the trial in mind.
  • The investigator and site personnel are properly trained on conducting the trial.
  • The appropriate regulatory documentation is collected and maintained.
  • Clinical data are being collected using Good Clinical Practices.
  • Adherence to study protocol and GCP
  • Safety data are being collected and reported to regulatory agencies
  • Data is collected, queried, and reported in an efficient manner.

To facilitate services in a timely and cost-effective manner, our staff is located throughout the country near most major medical facilities. Being therapeutically focused, our staff have worked with most of your important investigational sites for years on dozens of proocols. As an added benefit to saving our clients money through native efficiency, this rapport and respect with your sites ensures greater commitment to your study, faster recruitment and better responsiveness.

InFocus Clinical Research always customizes solutions to our partners study specifications in to increase efficiency and productivity. We provide our clients direct access to senior staff throughout the life of their project to ensure that any questions or issues related to the trial are addressed quickly.