IRB Coordinator job in Nashville, TN
Vacancy has expired
Nashville, TN CorTech LLC
| Job Ref: | 355243 |
| Employer: |
CorTech LLC |
| Job Type: | Contract |
| Salary and Benefits: | 27.00/Per Hour |
| Remote: | No |
Location |
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| City: | Nashville, TN |
| Post Code: | 37203 |
| Map: |
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Description |
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JobsRUs.com. is seeking to hire a IRB Coordinator for our client in Nashville, TN! Benefits Available! Weekly Pay! $27.00/Hour Job Description: Experience in clinical research, regulatory compliance, human research protections or IRB preferred. Ability to learn complex concepts (regulatory, ethical and scientific) and operate at a high level of interaction with researchers and board members. Required/preferred experience: Preferably more than 1 year of relevant experience. Experience in clinical research, regulatory compliance, human research protections or IRB preferred. Also, we need them to work late on most Fridays when there are new study documents that need to be uploaded and the system updated. Responsible for reviewing all submissions to the Institutional Review Board (IRB) to ensure that IRB members have all the requisite information to review human subject research; enabling the IRB board members, including the IRB Chairpersons, to perform their review tasks by providing the necessary documents and education; acting as intercessory between the boards, researchers and other involved institutions; and performing other related duties as assigned. Under minimal supervision, works to coordinate daily IRB activities to ensure protection of human subjects and compliance with laws and regulations related to human subject research conducted by the company and its affiliated network. Serves as resource related federal, state and institutional guidelines related to protection of human research subjects. Comprehensive understanding of Sarah Cannon Research Institute processes and operational goals. Knowledge: A body of information needed to perform tasks; May be obtained through education, training or experience. FDA and OHRP regulations governing human subjects research, and GCP guidelines Clinical research, regulatory compliance, human protections or IRB High level of proficiency with Microsoft Office | |
ref: (355243)
660 days ago
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