Clinical Research Coordinator-151534

Description & Requirements The Clinical Research Coordinator 2 is responsible for supporting a large, multi‑state study (BRITE Trial) focusing on school‑based suicide prevention programming. They will be responsible for the day‑to‑day implementation of the study protocol and data collection at the school sites. Research Coordinators/Interventionists will be certified to deliver the SOS Signs of Suicide (SOS) and Youth Aware of Mental Health (YAM) suicide prevention programs, completing study staff trainings for both interventions at the beginning of the study and participating in ongoing training and fidelity monitoring. They will be responsible for collecting measures related to the delivery of and fidelity to the study interventions. Frequent travel to school research sites around Central and Southern Idaho to engage with schools and to deliver the SOS and YAM study interventions to 8th, 9th, and 10th grade students will be required. The Research Coordinator/Interventionist will also facilitate the coordination of study recruitment, informed consent, and research visits/assessments for study participants at their assigned schools. Research Coordinators/Interventionists will serve as a resource for school partners as needed to provide problem‑solving assistance regarding study‑related procedures. They will be responsible for data collection, data entry, data proofing and cleaning, and resolving data queries. They will also be trained to follow study safety protocols for students screening at risk for suicide. They will support the data manager for the study, including support with data cleaning and basic data analysis. They will assist as needed with scheduling of meetings, taking meeting minutes, organization and distribution of study communications, conducting routine quality control processes, processing of travel reimbursements, and other administrative duties. Typical Hours Mon‑Fri ~8a‑4:30p, and flexibility to work earlier or later shifts as needed to accommodate engaged partners and school staff availability. Hours subject to change dependent on project needs. This position is temporary (5 years expected, depending on availability of grant funding). Preferred Qualifications Experience with and comfort working with groups of adolescents Comfort discussing suicide and mental health in a non‑judgmental environment Ability to thrive in a fast‑paced environment with multiple priorities Training in epidemiology, data science, or a related field Minimum Qualifications Education: Bachelor’s degree. Experience: 3 years’ experience. Licenses/Certifications: Current Basic Life Support (BLS) Provider Certified through American Safety and Health Institute, American Heart Association, or American Red Cross. What's In It For You At St. Luke’s, caring for people in the communities we serve is our mission – and this includes our own SLHS team. We offer a robust benefits package to support our teams both professionally and personally. In addition to a competitive salary and retirement plans, we ensure our team feels supported in their benefits beyond the typical medical, dental, and vision offerings. We care about you and have fantastic financial and physical wellness options, such as: on‑site massages, on‑site counseling via our Employee Assistance Program, access to the Personify Health Wellness tool, as well as other formal training and career development offerings to ensure you are meeting your career goals. St. Luke’s is an equal opportunity employer and does not discriminate against any person on the basis of race, religion, color, gender, gender identity, sexual orientation, age, national origin, disability, veteran status, or any other status or condition protected by law. Please note: this posting is not reflective of all job duties and responsibilities and is intended to provide an overview to job seekers. #J-18808-Ljbffr St. Luke's Health System