• Senior CMC Regulatory

    Insight Global (Rahway, NJ)
    Job Description Insight Global is looking for a Senior CMC Regulatory Specialist to join the Global Regulatory Affairs organization with a large ... products globally. This individual will be responsible for developing CMC regulatory strategies and authoring various .... Skills and Requirements - 5+ years experience in Regulatory Affairs within pharmaceutical industry - Extensive… more
    Insight Global (06/21/24)
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  • Sr. Specialist Regulatory

    Kedrion Biopharma, Inc. (Fort Lee, NJ)
    …Responsible for US change control assessment for assigned products. + Manage regulatory affairs activities including preparation of Annual Report, Change Control ... required, and the role will collaborate with tasks across the existing US Regulatory Affairs team Education/Experience: + BS/BA/MS degree in science. Minimum of… more
    Kedrion Biopharma, Inc. (04/02/24)
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  • Regulatory Affairs Ops…

    System One (Round Lake, IL)
    Title: Regulatory Affairs Ops Specialist II...scientific discipline + exp with drug solutions, FDA and CMC + 5 years regulatory experience within a ... Start: ASAP Duration: Contract Summary Joule has a contract opening for a Regulatory Affairs Ops Specialist II that will be responsible for the… more
    System One (06/17/24)
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  • Manager, Clinical Trials & Charge Capture

    Rush University Medical Center (Chicago, IL)
    …and coding. Certifications may include Certified Professional Coder (CPC), Certified Coding Specialist (CCS) and Certified Medical Coder ( CMC ), and any other ... communicates with Revenue Cycle colleagues, study teams, patients, Office of Research Affairs , IRB, RUMC Compliance, and all partners in the Research Continuum. *… more
    Rush University Medical Center (06/06/24)
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