... ) as they relate to the clinical trial management activities. • Responsible for development and ongoing maintenance of clinical study tools and templates, including the Clinical Monitoring Plan. Ensures CTMS, dashboards ...
... . Monitor appropriate sources for specific clinical study or federal regulation updates. Collect and enter study data into the appropriate system. • ...
... Medical Science Liaison (MSL) supports clinical study start-up, patient recruitment and retention, and study conduct from the medical scientific ...
... Investigator Study Coordinator Meetings and promote information sharing as needed Act as functional lead for process improvement initiatives Other accountabilities as assigned by Functional Manager in support of the business Y ou are: Clinical operations ...
... -up, organization and maintenance of clinical study documentation (e.g. Study Files, CRFs, etc.) and guidelines ( ...
... execution Responsible for management of study vendor Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables ...
... execution Responsible for management of study vendor Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables ...
... and pharmacovigilance issues. • Per the Clinical Monitoring Site Management Plan (CMP ... medical records o Verifies required clinical data entered in the case ... the effective conduct of the clinical study data review and capture o ...
... monitor multiple Phase II, III clinical trial sites, across different therapeutic ... strong relationship with investigators and study coordinators where respect, knowledge and commitment ... in the pharma or clinical research industry. Minimum 12 months ...
... The role: The Clinical Trial Manager is responsible for the delivery of all clinical aspects of the study. The CTM oversees the clinical portion of the budget, develops ... drive the clinical deliverables of a study • Subject matter expertise in the ...