Responsibilities
- 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
Qualifications
- 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