Job Description

Job Responsibilities:
• Searches peer-reviewed literature, Institutional Review Board (IRB) form submission, organizes and manages meetings pertaining to all research related projects.
• Edits posters and papers for publication.
• Collects data and surveys.
• Analyzes statistical and graphical data.
• Coordinates research and grant meetings.
• Coordinates clinical research trials.
• Conducts literature reviews.
• Manages and reconciles grant budgets, allocates monthly expenses, purchases research supplies, and creates workshop materials, accreditation applications, MURC invoices and deposits, quarterly reports, and cost sharing reports.
• Prints and binds coalition notebooks, generates quarterly reports, ships workshop materials, analyzes and manipulates data, and creates coalition newsletters.
• Manages workflows independently with excellent organization skills.
• Prioritizes quickly and appropriately with the ability to multi-task.
• Develops and/or maintains clinical research operational SOPs for the Division of Addiction Sciences.
• Maintains research equipment and storage facilities.
• Identifies new and potential clinical research related to the mission of the Division of Addiction Sciences.
• Performs other duties as assigned.

Education: Bachelor's degree in biological or chemical science, nursing, public health, or other healthcare related field. Master's degree in clinical research related field preferred
Experience: Preferred at least two years experience in coordinating clinical trials in an academic practice setting. Must be poised professional and able to communicate well, both verbally and in writing.

Internal applicants must call HR at ext. 11653 to determine eligibility before applying.