Project Management


  • Trial design and optimization

  • Investigator and site identification

  • Site contracts and payments

  • Presentations at symposia

  • Manuscript preparation

  • Clinical coordination


  • FDA and HIPAA compliance

  • Documentation following ICH and GCP guidelines

  • Site monitoring

  • Adverse event tracking and management

  • Progress reports and renewals

  • Support at FDA and international regulatory meetings

  • Project termination