• Sr. Clinical Team Manager (CTM)/ Prin. - Neurology

    ThermoFisher Scientific (Wilmington, NC)
    regulatory submissions (if appropriate) are addressed. Ensures that crucial document quality meets the expectation of Regulatory Compliance Review. Reviews ... digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities… more
    ThermoFisher Scientific (12/14/25)
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  • Registered Nurse - Plasma Center | Sign-On Bonus…

    BioLife Plasma Services (Pittsburgh, PA)
    …the role: Every day, the donors you meet will motivate you. The high- quality plasma you collect will become life-changing medicines. Here, a commitment to customer ... service and quality is expected. You will determine donor eligibility to...advanced knowledge of emergency care. * Ensures compliance with regulatory standards for plasma collection and maintains detailed documentation.… more
    BioLife Plasma Services (12/12/25)
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  • Senior Clinical Research Associate/Clinical…

    Parexel (Austin, TX)
    …of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical ... effective delivery of clinical trials (eg enrollment, database release), to safeguard the quality of investigator sites (eg patient safety, site quality and… more
    Parexel (12/07/25)
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  • Sanitation Manager

    Rise Baking Company (Pleasant View, UT)
    …allergen controls, pest controls, traffic control, internal audits, food safety and quality management systems, and regulatory compliance o Proper record-keeping ... was founded by bakery experts passionate about providing our customers with high quality products and providing a positive, collaborative place to work for our… more
    Rise Baking Company (12/04/25)
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  • Vendor Management Specialist

    Charles River Laboratories (Charleston, SC)
    …improvements * Experience with change management and ensuring compliance with quality assurance (QA) and regulatory requirements, especially concerning supplier ... issues and customer pain points related to instruments. * Liaise with the Quality Assurance (QA) team on change management processes and ensure all Supplier … more
    Charles River Laboratories (11/14/25)
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  • QC Supervisor

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …experience required, or equivalent experience in leading projects. + Knowledge of the FDA medical device quality system regulations and international quality ... **Job Description Summary** Quality Control (QC) Supervisor is responsible for leading...complies with those regulations, practices and procedures to support regulatory compliance requirements. Communicates the need for compliance to… more
    BD (Becton, Dickinson and Company) (11/10/25)
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  • ATSU - Research Project Coordinator II

    AT Still University (Mesa, AZ)
    …investigator(s) and other key stakeholders (eg, research team members, funders, regulatory bodies) on study-specific research processes. + Research study data ... collection planning, including data management and data quality management. + Processing collected data using project-specific procedures and technology. + Recruit,… more
    AT Still University (12/26/25)
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  • Medical Writer II

    Adecco US, Inc. (Morristown, NJ)
    …with digital marketing strategies and SEO best practices. + Working knowledge of FDA , EMA, or other global regulatory guidelines for healthcare communications. + ... medical information into clear, audience-appropriate messaging while adhering to regulatory standards. **Pay** 60-69/hr depending on education and experience… more
    Adecco US, Inc. (12/19/25)
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  • Research Scientist I - Bioanalytical Science

    Charles River Laboratories (Reno, NV)
    …study management, interpretation and reporting of study data, and assuring the regulatory compliance of these projects. We are seeking a **Research Scientist I ... management, interpretation and reporting of study data, and assuring the regulatory compliance of these projects, as appropriate. Additional responsibilities include… more
    Charles River Laboratories (12/19/25)
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  • Sr. Director, Clinical Pharmacology…

    Taiho Oncology (Princeton, NJ)
    …Plans. + Collaborating with Clinical Development, Biostatistics, Clinical Operations and Regulatory to incorporate the bioanalysis for PK and CP components and ... of the following documents: + Clinical Study Reports. + Investigator Brochures. + Regulatory Documents, including NDAs and MAAs and responses to questions from … more
    Taiho Oncology (12/19/25)
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