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Clinical Research Protocol Navigator
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- Work Details:Develop and review completed new and amended clinical research protocols and related documentation throughout the lifecycle of the study, with special attention to the accuracy, consistency, and completeness of documents.
- Develop new and review completed clinical research informed consent and other ethics and regulatory related documentation.
- Maintain all regulatory trial documentation including maintaining a complete and up-to-date Regulatory Binder for each trial, documentation of investigator qualifications, trial logs and safety reports.
- Assists researchers with protocol development, assembly and review of clinical trial documents.
- Assist researchers develop, prepare internal research proposals, abstract submissions, poster presentations and manuscript drafts.
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