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Position Summary:
Prepares, submits and maintains clinical trials regulatory data and documents. Initiates and maintains all Regulatory documents necessary for submission to Institutional Review Boards, study sponsors, and various agencies in order to obtain initial and continued approval of all clinical trials. This position functions as an integral part of a project team whose objective is to assist study sponsors, physicians, and patients enroll and complete clinical research trials. This position is responsible for all regulatory document coordination, filing, monitoring and reporting to the project team regarding regulatory information. The Regulatory Coordinator also receives, processes, distributes, and manages clinical trial safety reporting.
Position Qualification:
Required:
1-3 years experience in clinical, research, and/or regulatory support role.
Full Time
$51k-66k (estimate)
12/15/2023
05/05/2024
ms.utmck.edu
Knoxville, TN
<25
The job skills required for Regulatory Coordinator include Clinical Research, Clinical Trial, Coordination, Microsoft Word, etc. Having related job skills and expertise will give you an advantage when applying to be a Regulatory Coordinator. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Regulatory Coordinator. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Regulatory Coordinator positions, which can be used as a reference in future career path planning. As a Regulatory Coordinator, it can be promoted into senior positions as a Regulatory Affairs Specialist II that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Regulatory Coordinator. You can explore the career advancement for a Regulatory Coordinator below and select your interested title to get hiring information.