Regulatory Affairs Specialist - Seattle - Providence

    Providence
    Providence Seattle

    1 week ago

    Providence background
    Full time
    Description

    Regulatory Affairs Specialist - Clinical Research

    We are seeking a detail-oriented Regulatory Affairs Specialist to join our clinical research team in Swedish Cherry Hill. This is a full-time position working 8:00 AM to 5:00 PM PST (Mondays to Fridays).

    Key Responsibilities:

    • Prepare, facilitate, coordinate, and submit documentation required by federal, state, and local regulations and institutional requirements relating to the conduct of research.
    • Coordinate IRB submissions to assure the protection of human subjects in research; FDA-required submissions including investigator 1572 forms, investigational new drug applications, device submissions, and other documents required by regulatory agencies or institutions.
    • Lead Research Assistants on a task-basis if applicable; provide on-the-job training, set priorities, and schedule workflow required to support project objectives.

    Requirements:

    • Bachelor's Degree in science, healthcare, or related field or significant experience in research coordination or regulatory work may be substituted for educational requirements.
    • 2 years experience in healthcare, research, or clinical setting with regulatory compliance familiarity.

    Salary Range:

    $65,000 - $90,000 per year

    About {company}

    {company} values its employees and offers a comprehensive benefits package, professional growth opportunities, and a supportive work environment.

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