• Investigator Senior

    State of Minnesota (St. Paul, MN)
    **Working Title: Senior Investigator ** **Job Class: Investigator Senior ** **Agency: Labor & Industry Dept** + **Job ID** : 87675 + **Location** : St. ... building officials, and manufactured home dealers, manufacturers, and installers. Senior Investigators plan and initiate comprehensive investigations and mediations… more
    State of Minnesota (09/04/25)
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  • Investigator Senior

    State of Minnesota (St. Paul, MN)
    **Working Title: Investigator Senior ** **Job Class: Investigator Senior ** **Agency: Public Employment Relations Board** + **Job ID** : 87876 + ... **Location** : St. Paul + **Telework Eligible** : Yes + **Full/Part Time** : Full-Time + **Regular/Temporary** : Unlimited + **Who May Apply** : Open to all qualified job seekers + **Date Posted** : 07/30/2025 + **Closing Date** : Open until filled. First… more
    State of Minnesota (07/31/25)
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  • Senior Fire Investigator , Iaai-CFI

    EFI Global (St. Paul, MN)
    …and ethical manner.** **May provide investigative guidance to Fire Investigator team members.** **ADDITIONAL FUNCTIONS and RESPONSIBILITIES** **Performs other duties ... **Minimum certification requirement for consideration, Certified Fire & Explosion Investigator (CFEI).** **IAAI Certified Fire Investigator (IAAI-CFI)… more
    EFI Global (09/06/25)
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  • Senior Investigation and Resolution…

    Metropolitan Council (St. Paul, MN)
    …the communities we serve. We are currently seeking an EO Consultant III - Senior Investigator . The Office of Equity and Equal Opportunity (OEEO) supports the ... work would contribute to our organization and the Twin Cities region: The senior investigator works in the Office of Equity and Equal Opportunity (OEEO)in the… more
    Metropolitan Council (09/09/25)
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  • Senior Manager, Clinical Project Management

    Sumitomo Pharma (St. Paul, MN)
    …conducted in compliance with the agreed study plans through regular CRO and/or investigator site contact. + Monitors progress of clinical activity and reports on the ... status of clinical data collection of assigned clinical trials. + Prepares potential investigator site lists and assists with their evaluation for inclusion in the… more
    Sumitomo Pharma (09/03/25)
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  • Senior Principle Scientist, Regulatory…

    Merck (St. Paul, MN)
    …+ Worldwide marketing applications + Clinical study protocols and reports + Investigator brochures + Local registration study protocols for secondary markets + ... Represent Global Regulatory Affairs on internal committees (eg, DRC, ADT/PDT, EDT, LEAD) to provide strategic regulatory input and approvals. + Conduct initial content review and approval for IND/CSA submissions to enable clinical trial initiation. +… more
    Merck (08/23/25)
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  • Executive Director, Scientific Affairs,…

    Merck (St. Paul, MN)
    …and to improve outcomes for patients. The EDSA leads a large investigator -initiated studies program in partnership with late-stage development teams in Medical ... Congress summary reports. **Primary Responsibilities:** + Leads our Company's Investigator Initiated Studies program in assigned therapeutic areas ensuring… more
    Merck (09/06/25)
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  • Associate Medical Director, Pharmacovigilance…

    Sumitomo Pharma (St. Paul, MN)
    …evaluation reports according to established safety governance policies and keeping senior leadership informed of safety issues. **Job Duties and Responsibilities** + ... Forms (ICF), Safety Management Plans (SMP), Clinical Study Reports (CSR), Investigator 's Brochures (IB), Investigator communications (Dear Health Care Provider… more
    Sumitomo Pharma (08/15/25)
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  • Director, Clinical Operations

    Bausch + Lomb (St. Paul, MN)
    …ensure study objectives are being met and provide the operations director and/or senior management with timely updates on progress and changes in scope, schedule, ... and resources. + Organize investigator and expert meetings relevant to the indication and...handled by the CRAs and responded to by the site/ investigator in a timely manner. May assist in the… more
    Bausch + Lomb (09/06/25)
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  • Director, Regulatory Affairs

    Sumitomo Pharma (St. Paul, MN)
    …CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/data) and contributes to content as needed ... CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/data) and contribute to content as needed… more
    Sumitomo Pharma (09/09/25)
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