... , you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with ...
... Responsibilities: Clinical Trial Monitoring: Conduct site initiation, routine monitoring, and close-out visits to ensure protocol compliance and data integrity. Perform source document verification, review of case report forms, and data validation. Monitor ...
... Responsibilities: Clinical Trial Monitoring: Conduct site initiation, routine monitoring, and close-out visits to ensure protocol compliance and data integrity. Perform source document verification, review of case report forms, and data validation. Monitor ...
... Responsibilities: Clinical Trial Monitoring: Conduct site initiation, routine monitoring, and close-out visits to ensure protocol compliance and data integrity. Perform source document verification, review of case report forms, and data validation. Monitor ...
... Responsibilities: Clinical Trial Monitoring: Conduct site initiation, routine monitoring, and close-out visits to ensure protocol compliance and data integrity. Perform source document verification, review of case report forms, and data validation. Monitor ...
... Responsibilities: Clinical Trial Monitoring: Conduct site initiation, routine monitoring, and close-out visits to ensure protocol compliance and data integrity. Perform source document verification, review of case report forms, and data validation. Monitor ...
... Responsibilities: Clinical Trial Monitoring: Conduct site initiation, routine monitoring, and close-out visits to ensure protocol compliance and data integrity. Perform source document verification, review of case report forms, and data validation. Monitor ...
... Responsibilities: Clinical Trial Monitoring: Conduct site initiation, routine monitoring, and close-out visits to ensure protocol compliance and data integrity. Perform source document verification, review of case report forms, and data validation. Monitor ...
... Responsibilities: Clinical Trial Monitoring: Conduct site initiation, routine monitoring, and close-out visits to ensure protocol compliance and data integrity. Perform source document verification, review of case report forms, and data validation. Monitor ...
... Responsibilities: Clinical Trial Monitoring: Conduct site initiation, routine monitoring, and close-out visits to ensure protocol compliance and data integrity. Perform source document verification, review of case report forms, and data validation. Monitor ...