We are currently seeking a Senior CRA to assist in the development, implementation and execution of study protocols and associated study documents for clinical trials and marketing studies, with primary emphasis on monitoring oversight of IDE clinical trials, including development of monitoring plans and review of all monitoring reports. Sr. CRA will assist in the clinical monitoring of all studies including the coordination of site activities from site start-up to site closure as needed. Will work ...
Looking for a Regulatory Submissions Manager to work for an amazing client with great benefits! My client is looking to interview and hire immediately for the right person. Please send me your resume for consideration if you are interested!
Regulatory Submissions Manager
Efficiently manage and successfully execute all aspects of global start-up according to Sponsor specifications;
Perform quality checks on submission documents and site essential documents;
Interact with US central ...
Our client, a top pharmaceutical company, is looking for a Clinical Research Associate in Cincinnati, OH.
This is a 100% REMOTE position.
Responsible for initiation, monitoring, completion, and reporting of clinical trials under direct supervision.
•Monitor the general progress of trials, e.g., patient enrollment, administrative activities.
•Assist in preparation of case report forms, investigator brochures and related documentation by coordinating and utilizing input from ...
Apr 3 -
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