Regulatory Affairs Specialist, Clinical Research
Alcanza Clinical Research
Alcanza Clinical Research is seeking a Regulatory Specialist to support GCP and SOP compliance across a growing multi-site network. You will maintain essential regulatory documents and liaise with IRBs and sponsors. This role requires a Bachelor's degree and at least 1 year of clinical research regulatory experience, with strong attention to detail and the ability to train staff on regulatory processes. Join Alcanza Corporate as part of the Regulatory team to help ensure quality, compliance, and #J-18808-Ljbffr Alcanza Clinical Research
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