Research Services Entry Professional

University of Colorado•Aurora, CO

1d•$24,950 - $31,736•Onsite

About The Position

The Department of Psychiatry is hiring a 0.5 FTE (benefits eligible) Professional Research Assistant to contribute to two projects. The first is an innovative, grant-funded implementation study focused on improving perinatal mental health and perioperative experiences for patients and families. The second is a diagnostic device study which uses eye metrics to diagnose Post-Traumatic Stress Disorder (PTSD). The PRA will be embedded in Psychiatry Research Innovations (PRI), a research support center within the Department of Psychiatry that assists faculty members affiliated with five Divisions in the Department in areas related to research administration, operations, and education. This position supports research that advances patient-centered care and innovation.

Requirements

Bachelor’s degree in public health, social/behavioral sciences, physical sciences, nursing, healthcare, or a directly related field from an accredited institution.
A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor’s degree on a year for year basis.
An advanced degree (Masters or Doctorate) may be substituted for experience on a year for year basis if the degree is in a field of study directly related to the work assignment.
Applicants must meet minimum qualifications at the time of hire.
Knowledge and understanding of federal regulations and Good Clinical Practice (GCP)
Ability to communicate effectively, both in writing and orally
Ability to establish and maintain effective working relationships with employees at all levels throughout the institution
Outstanding customer service skills
Demonstrated commitment and leadership ability to advance diversity and inclusion
Knowledge of basic human anatomy, physiology, medical terminology
Ability to interpret and master complex research protocol information
Applicants must be legally authorized to work in the United States without requiring sponsorship. We are unable to provide work visa sponsorship or employment authorization for this position now or in the future.

Nice To Haves

One (1) year of clinical research or related experience.
Prior experience supporting research or clinical care with perinatal, obstetric, or NICU populations.
Prior experience supporting research or clinical care with psychiatric populations with mood disorders, anxiety disorders, and/or trauma- and stressor-related disorders

Responsibilities

Obtain study subject’s medical history and current medication information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial.
Perform informed consent process or ensures that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required.
Schedule subject participation in research clinical trial, coordinating availability of necessary space, and clinical research support (e.g., physician, nurse practitioner, laboratory, radiology, pharmacy).
Guide participants through study activities and visits, including overseeing survey completion, administering various research scales and assessments, and providing instructions and basic troubleshooting.
Collect, code, and analyze data obtained from research in an accurate and timely manner.
Adhere to research regulatory standards.