Research Data & Quality Control Coordinator

St Luke; Boise (ID); On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

On-site massages

On-site counseling via EAP

Wellness tool access

Training and career development

Job summary

St. Luke's in Idaho is seeking a Research Coordinator 2 to support the BRITE Trial, a large school-based suicide prevention study across multiple states.

You will ensure day-to-day adherence to the study protocol and help manage data collection, participant tracking, and study communications. The role involves coordinating recruitment, informed consent, travel reimbursements, and occasional delivery of SOS/YAM interventions at partner schools.

Qualifications

• 3 years' experience in research coordination.
• Current Basic Life Support (BLS) certification.
• Experience supporting human subjects research.
• Ability to work in a fast-paced environment with multiple priorities.
• Strong organizational skills with attention to detail.

Responsibilities

• Support day-to-day adherence to the BRITE trial protocol.
• Develop and oversee routine quality control processes.
• Manage participant compensation and retention tracking.
• Coordinate scheduling, meetings, minutes, and communications.
• Assist with data collection, data entry, cleaning, and queries.
• Travel to school research sites as needed to deliver interventions.

Skills

Human subjects research

Large studies experience

Multitasking

Organizational skills

Attention to detail

Education

BLS certification

Job description

Research Coordinator for School-Based Suicide Prevention Trial

At St. Luke's, we pride ourselves on fostering a workplace culture that values diversity, promotes collaboration, and prioritizes employee well-being. Our commitment to excellence in patient care extends to creating an environment where our team can thrive both personally and professionally. With opportunities for growth, competitive benefits, and a supportive community of colleagues, St. Luke's is truly a great place to work.

What to Expect:

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 adherence to the study protocol and developing and overseeing routine quality control processes, overseeing participant compensation, tracking participant retention, and supporting data management. The Research Coordinator will also be responsible for sites managing study-related administrative processes such as scheduling meetings, taking meeting minutes, organization and distribution of study communications, processing of travel reimbursements, and other administrative duties.

The Research Coordinators may be certified as a back-up Interventionist 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. Some 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 may be required.

The Research Coordinator may also facilitate the coordination of study recruitment, informed consent, and research visits/assessments for study participants in schools. They will support data collection, data entry, data proofing and cleaning, and resolving data queries.

Typical hours

Mon-Fri ~8a-4:30p, and flexibility to work earlier or later shifts as needed to accommodate study needs. This position is temporary (5 years expected, depending on availability of grant funding).

Preferred Qualifications:

• Experience supporting human subjects research studies. Experience with large, complex studies preferred.
• Comfort discussing suicide and mental health in a non-judgmental environment.
• Ability to thrive in a fast-paced environment with multiple priorities.
• Efficient and able to balance multiple responsibilities.
• Strong organizational skills with attention to detail.

Minimum Qualifications:

• 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

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,
• 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.