What are the responsibilities and job description for the Clinical Research Coordinator 253251 position at Medix™?
- Participant pre-screening, recruitment and scheduling
- Complete protocol and trial system training
- Maintenance of regulatory documents
- Conducts or participates in the informed consent process and discussions with trial participants, including answering any questions related to the study.
- Conducting participant visits
- Ability to perform basic lab and clinical procedures
- Entering data in the EDC and resolving all queries
- Updating and maintaining trial logs and participant charts
- Conducting monitoring visits
- Managing and reporting of AEs, SAEs, and deviations
- Maintains adequate inventory of study supplies
- Coordinates appropriate and timely payments to participants
- Manages and maintains all regulatory information about the study including the protocol
Salary : $30 - $34