• Senior Scientific Associate

    Henkel (Chanhassen, MN)
    Senior Scientific Associate **_About_** **_this_** **_position_** At Henkel, you'll be part of an organization that's shaping the future through innovation, ... Collaborate with other PD (product development) and cross-functional team members: supporting senior team leaders and guiding junior members as needed. + Ensures… more
    Henkel (12/02/25)
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  • Senior Clinical Research Associate

    Parexel (St. Paul, MN)
    **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical ... May undertake the responsibilities of an unblinded monitor where appropriate **Clinical/ Scientific and Site Monitoring Risk** + Maintain thorough understanding of… more
    Parexel (12/07/25)
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  • Senior Clinical Research Associate

    Parexel (St. Paul, MN)
    The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the ... other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are...for the local market. + Collaborates with local Medical Scientific Liaisons (MSLs) as directed by LSAD or line… more
    Parexel (12/03/25)
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  • Senior Medical Writer - US - FSP

    Parexel (St. Paul, MN)
    **Job Summary:** The Senior Medical Writer will research, create, and edit all documents associated with clinical research. Responsibilities also include: acting as ... of documentation by Medical Writing Support Coordinator, Document Specialist, and/or Associate Medical Writer for assembly of project files and client deliverables.… more
    Parexel (12/13/25)
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  • Sr. Clinical Research Associate - Oncology…

    Parexel (St. Paul, MN)
    The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator ... May undertake the responsibilities of an unblinded monitor where appropriate **Clinical/ Scientific and Site Monitoring Risk:** + Maintain thorough understanding of… more
    Parexel (12/11/25)
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  • Associate Clinical Site Lead

    Abbott (Minneapolis, MN)
    …people with diabetes from routine fingersticks. Summary Under the supervision of senior colleague/manager (or delegate), the Associate Clinical Site Lead drives ... or competent authority/ethics committee. Main Responsibilities Under supervision of senior colleague/manager (or delegate): Develop and support a productive clinical… more
    Abbott (12/12/25)
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  • Senior Supplier Quality Engineer

    Danaher Corporation (Chaska, MN)
    …System (http://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Senior Supplier Quality Engineer for Beckman Coulter ... implement lean processes, and eliminate waste to enhance production efficiency and associate engagement. The essential requirements of the job include: + … more
    Danaher Corporation (10/19/25)
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  • Associate / Medical Director - Rheumatology…

    Parexel (St. Paul, MN)
    …we are expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of our Global Immunology and Inflammation ... Therapeutic Franchise. As an Associate / Medical Director, you will work closely with...any matters pertaining to safety of study participants and scientific integrity of the study + Attending and supporting… more
    Parexel (10/11/25)
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  • Associate Director, Regulatory Affairs…

    Sumitomo Pharma (St. Paul, MN)
    …a dynamic, highly motivated, and experienced individual for the position of ** Associate Director, Regulatory Affairs (Oncology).** The Associate Director is part ... positions. + Comfortable presenting to all levels of the organization including Senior Management. **Education and Experience** + Bachelor's degree in a related… more
    Sumitomo Pharma (10/11/25)
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  • Regulatory Affairs Associate Director, IVD

    GRAIL (St. Paul, MN)
    …manage and provide direction to regulatory staff and, when required, participate in senior management meetings as a delegate. The role fosters a work culture aligned ... Maintain up-to-date knowledge of applicable regulatory requirements and relevant scientific /technical developments. + Identify regulatory risks and propose alternative… more
    GRAIL (12/03/25)
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