IRB Regulatory Coordinator Temp Needed in West Los Angeles
Growing Oncology Clinical Trial site needs a temporary IRB Regulatory Coordinator in the west side of Los Angeles. This is a temp to hire position.
- Will provide support for clinical research protocols, informed consents, etc.
- Will assist with all aspects of clinical research regulatory to ensure compliance to regulations and protection of human subjects
- Prepare and submit documents to the IRB
- Bachelor’s degree required
- 1+ years of IRB/Regulatory experience required
- Oncology experience is preferred
- SoCRA or ACRP is preferred
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- Submit your resume /Contact Paul
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Contact Paul/Submit Your Resume
[indeed-apply jobtitle=”IRB” emailapplicationto=”firstname.lastname@example.org”]
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