• CRNA UPMC

    UPMC (Altoona, PA)
    …regulatory compliance standards + Participate in the Quality Improvement (QI) process through documentation , incident reporting, evaluation, education, and ... to established policies, procedures, and regulatory standards. Review appropriate documentation for informed consent and identify appropriate surgical site with… more
    UPMC (11/12/25)
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  • CRNA UPMC St. Margaret

    UPMC (Pittsburgh, PA)
    …regulatory compliance standards + Participate in the Quality Improvement (QI) process through documentation , incident reporting, evaluation, education, and ... to established policies, procedures, and regulatory standards. Review appropriate documentation for informed consent and identify appropriate surgical site with… more
    UPMC (11/12/25)
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  • CRNA, UPMC Shadyside, Casual

    UPMC (Pittsburgh, PA)
    …regulatory compliance standards + Participate in the Quality Improvement (QI) process through documentation , incident reporting, evaluation, education, and ... to established policies, procedures, and regulatory standards. Review appropriate documentation for informed consent and identify appropriate surgical site with… more
    UPMC (11/12/25)
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  • CRNA, Casual, UPMC

    UPMC (Somerset, PA)
    …regulatory compliance standards + Participate in the Quality Improvement (QI) process through documentation , incident reporting, evaluation, education, and ... to established policies, procedures, and regulatory standards. Review appropriate documentation for informed consent and identify appropriate surgical site with… more
    UPMC (11/12/25)
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  • CRNA UPMC Children's Hospital of

    UPMC (Pittsburgh, PA)
    …regulatory compliance standards + Participate in the Quality Improvement (QI) process through documentation , incident reporting, evaluation, education, and ... to established policies, procedures, and regulatory standards. Review appropriate documentation for informed consent and identify appropriate surgical site with… more
    UPMC (11/12/25)
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  • CRNA UPMC East

    UPMC (Monroeville, PA)
    …regulatory compliance standards + Participate in the Quality Improvement (QI) process through documentation , incident reporting, evaluation, education, and ... to established policies, procedures, and regulatory standards. Review appropriate documentation for informed consent and identify appropriate surgical site with… more
    UPMC (11/12/25)
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  • Quality Program Manager

    Catalent Pharma Solutions (Philadelphia, PA)
    …as the primary contact with clients if there are quality questions on documentation , process questions, issues, etc + Be knowledgeable about customer-specific ... visits to ensure that the client receives any appropriate documentation requested and get questions answered + Act as...requirements. Ensure they are built into the process and communicated to relevant Catalent staff + Review… more
    Catalent Pharma Solutions (11/26/25)
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  • Quality Program Manager

    Catalent Pharma Solutions (Philadelphia, PA)
    …as the primary contact with clients if there are quality questions on documentation , process questions, issues, etc + Be knowledgeable about customer-specific ... visits to ensure that the client receives any appropriate documentation requested and get questions answered + Act as...requirements. Ensure they are built into the process and communicated to relevant Catalent staff + Review… more
    Catalent Pharma Solutions (11/26/25)
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  • Regulatory Affairs Specialist-CC

    University of Pennsylvania (Philadelphia, PA)
    …Manager, the Regulatory Affairs Specialist-CC will, with minimal supervision, prepare and process all regulatory documentation through the IRB, CTSRMC, FDA and ... and reportable events. He/she will, with minimal supervision, prepare and process all required regulatory documentation for pharmaceutical companies, contract… more
    University of Pennsylvania (12/14/25)
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  • Clinical Research Coordinator C (Department…

    University of Pennsylvania (Philadelphia, PA)
    …in the coordination of Phase I-IV clinical trials (10% Essential: 1),Prepare and process all regulatory documentation through the IRB, CTSRMC, FDA and all ... to protocol requirements + Organize and maintain all required documentation - including source documentation , case report forms,...Complete case report forms and resolve data queries + Process and ship study specimens including blood, urine and… more
    University of Pennsylvania (12/10/25)
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