Who should attend?




This event will particularly benefit professionals involved in the planning, logistics, management and implementation of e-clinical trials. It will introduce new e-clinical professionals to the entire scope of their responsibilities, and upgrade the knowledge base of experienced clinical supply professionals with new technologies and processes.   From pharmaceutical, biotech and CROs:
   
 
  • Clinical Project Leaders
  • Heads of Clinical Operations
  • Heads of Clinical Research
  • Clinical Research Associates
  • Clinical Trials Managers
  • Clinical/Site Monitors
  • Regulatory Managers
  • Clinical Auditors
  • Heads of Quality Control/Assurance/GCP
  • Compliance
  • Clinical Statisticians
  • Programmers
  • Clinical Data Managers/Coordinators
  • Clinical IT Managers
  • Clinical/Medical Advisors
  • Investigators