• To verify the conduct of the study is compliant with the protocol, GCP, and regulatory requirement(s)
  • To verify that the rights and wellbeing of clinical study participants are protected and to conduct monitoring to confirm safety and data integrity
  • To identify investigators and verify that they have adequate qualifications and resources and that laboratories, equipment, and staff are adequate
  • To act as the main point of communication with the investigator and team


  • College/university degree in life sciences or equivalent experience
  • On-site monitoring experience
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills