Jobs · Analyst · Missouri

Clinical Trials Coordinator (Research Specialist II)

University of Missouri-Columbia · Columbia, MO · 1 mo ago
Analyst$19.25–$27.4/hrFull-time
  • Education, certification, or professional training in research administration or project management.
  • The successful candidate will be highly organized, detail-oriented, and able to manage multiple studies while communicating effectively with scientific, clinical, administrative, and external partners.
  • Pay

    Anticipated Hiring Range Salary range: $19.25 - $27.40 per hour GGS Grade: 008 University Title: Research Specialist II Internal applicants can determine their university title by accessing the Talent Profile tile in myHR.

    Schedule

    Typical hours are Monday through Friday: 8:00am to 5:00pm.

    Benefits

    This position is eligible for University benefits. As part of your total compensation, the University offers a comprehensive benefits package, including medical, dental and vision plans, retirement, paid time off, short- and long-term disability, paid parental leave, paid caregiver leave, and educational fee discounts for all four UM System campuses. For additional information on University benefits, please visit the Faculty & Staff Benefits website at https://www.umsystem.edu/departments-staff/human-resources/benefits-retirement

    Employment visa sponsorship is not available for this position.

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    About the role

    The College of Veterinary Medicine at MU is on a mission to educate and train outstanding clinicians and scientists, generate new knowledge, engage stakeholders, and foster economic growth, all of which promote and protect the health and welfare of animals and people. Simply put, our mission is to Teach, Heal, Discover and Serve.

    Responsibilities

    • Coordinate study feasibility, startup, activation, implementation, day-to-day management, and closeout across multiple clinical services.
    • Prepare, submit, and maintain study, regulatory, and compliance documentation, including ACUC/IACUC submissions, amendments, informed client consent forms, study files, SOPs, templates, and required approvals.
    • Assist faculty investigators with proposal preparation, study design logistics, feasibility review, and development of study workflows that support successful clinical trial conduct

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