... 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 ...
... , 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 ...
... , 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 ...
... life-changing therapies to marketCTI Clinical Trial and Consulting Services#J-18808- ...
... an inclusive environment. From the Clinical Operations department we are looking for a Clinical Trial Assistant. Your main mission will ... (s) in the execution of clinical trials. This includes maintaining the Trial Master File (TMF) in an ...
... , you will independently control and monitor investigation sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with ...
... and external stakeholdersManage clinical portion of the trial in a patient centric approach and proactively identifying risk, potential patient safety events, and maintain oversight for data integrity. Successfully oversee and monitor CRAs in a matrix ...
... Electronic Laboratory Notebooks (ELN), Clinical Research Organization (CRO) integration, Clinical Trial Management Systems (CTMS), and Statistical ... SaaS platforms such as Clinical Trial Management Systems (CTMS), Electronic Trial Master File (eTMF) etc to ...
... , you will independently control and monitor investigation sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with ...