Academic/Faculty/Research Physician - Minneapolis - Medix

    Medix
    Medix Minneapolis

    1 week ago

    Description
    Lead Principal Investigator (PI) MD/DO

    Location:
    Minneapolis, Minnesota 55403

    Employment Type:
    Direct Hire, W-2

    Schedule:
    Full-Time, Monday Friday, 9:00 AM 5:00 PM

    Relocation Assistance:
    Available for qualified candidates

    Annual Salary:
    $200,000 $300,000

    Specialties Preferred:
    Neurology, Psychiatry, Family Medicine, Internal Medicine, Emergency Medicine

    Clinical Trials:
    Alzheimer's Disease, Psychiatry

    About the Opportunity
    Medix is partnered with a multi-site clinical research organization supporting industry-sponsored pharmaceutical clinical trials. This

    Principal Investigator (MD/DO)

    opportunity is ideal for an experienced physician who is interested in


    partnering to launch and grow a new clinical research site , while leveraging the operational infrastructure, sponsor relationships, and support of an established research organization.

    This role offers a unique opportunity for a PI who enjoys

    hands-on clinical research , values high-quality patient care, and is motivated by the chance to help

    build a site from the ground up

    with long-term growth potential.
    Overview
    The

    Principal Investigator (MD/DO)

    serves as the medical and scientific lead for clinical trials conducted at the research site.

    The PI is responsible for ensuring subject safety, protocol compliance, data integrity, and regulatory adherence, while providing comprehensive medical oversight throughout the conduct of clinical studies.

    Key Responsibilities
    Serve as the Principal Investigator of record for assigned industry-sponsored clinical trials
    Provide medical oversight and clinical decision-making for study participants, including management of comorbid conditions
    Ensure trials are conducted in compliance with ICH-GCP, FDA regulations, IRB requirements, and sponsor protocols
    Perform or supervise protocol-required clinical assessments and study procedures
    Review and assess adverse events (AEs), serious adverse events (SAEs), and safety data, ensuring timely and accurate reporting
    Lead and collaborate with sub-investigators, study coordinators, and site staff
    Participate in site initiation visits, monitoring visits, audits, and inspections
    Communicate effectively with sponsors, CROs, and regulatory authorities
    Maintain accurate and complete source documentation and regulatory files
    Contribute to the development, growth, and long-term success of a newly launched research site
    Required Qualifications
    MD or DO with board certification (or eligibility) in Neurology, Psychiatry, Family Medicine, Internal Medicine, or Emergency Medicine
    Active, unrestricted Minnesota Medical License, or eligibility to obtain
    Demonstrated experience serving as a Principal Investigator on industry-sponsored pharmaceutical clinical trials (required)
    Strong understanding of clinical research regulations, GCP, and FDA requirements
    Interest in partnering with an established clinical research organization to launch and build a new site from the ground up
    Excellent communication, leadership, and collaborative skills
    Why This Role Is Unique
    Opportunity to help launch and shape a new clinical research site
    Backed by the infrastructure, operational support, and sponsor relationships of an established multi-site organization
    Ability to expand long-term involvement in clinical research and site leadership
    Meaningful impact on patient access to innovative therapies

    Interested in learning more about this opportunity or exploring other Principal Investigator opportunities with Medix nationwide? Apply today to start the conversation.


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