• Remote Prior Authorization

    Insight Global (Eden Prairie, MN)
    Job Description An employer is looking for a highly skilled remote Prior Authorization Regulatory Specialist to join one of our largest national ... professional experience working within the prior authorization process specifically within a regulatory environment...prior authorization process specifically within a regulatory environment will help you be successful on this… more
    Insight Global (10/04/24)
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  • Senior Principal Regulatory Affairs…

    Medtronic (Minneapolis, MN)
    …MN but a remote worksite may be considered. The **Senior** **Principal Regulatory Affairs** will play a key role in providing regulatory affairs support ... timely approvals to support clinical studies and market releases. + Negotiate with regulatory authorities to resolve questions/issues that arise prior to and… more
    Medtronic (09/17/24)
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  • Director, Specialty Clinical Solutions- RPH/PharmD…

    Prime Therapeutics (St. Paul, MN)
    …Manages current clients in all Medical Pharmacy programs such as Fee Schedule Management, Prior Authorization , Post Service Claim Edits, Site of Service and any ... **Job Posting Title** Director, Specialty Clinical Solutions- RPH/PharmD required- REMOTE **Job Description Summary** Responsible for support and development of… more
    Prime Therapeutics (08/23/24)
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  • Remote - Licensed Mental Health…

    Fairview Health Services (St. Paul, MN)
    …more information: Fairview Benefits (https://www.fairview.org/benefits/noncontract) Schedule: This 1.0 FTE Remote position works Monday through Friday 7:30 am to ... Maintains required, appropriate, and timely communication and correspondence with treatment authorization and payer sources in a manner which promotes efficient and… more
    Fairview Health Services (07/30/24)
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  • Clinical Research Manager - Structural Heart

    Medtronic (Mounds View, MN)
    …Click Here (https://www.medtronic.com/us-en/about/careers/diversity-inclusion.html) **Location:** Mounds View, MN. Remote option available. **Travel:** up to 25% ... for the conduct of clinical studies and for the regulatory affairs function as it applies to product approval....Plan (study protocol, Instructions For Use (IFU), report of prior Investigations, bibliography, Case Report Forms (CRFs), etc.) and… more
    Medtronic (08/17/24)
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