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Clinical Research Coordinator 1

St. Luke's Health System

Boise, IDJobSeen 5 days agoSeen in employer's feed 5 days ago

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At a glance

Compensation
No compensation found
Location
Boise, ID
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Requirements

Credentials this posting asks for.

Basic Life Support CertificationBachelor's degree

Job overview

The Clinical Research Coordinator 1 supports studies across the Research Department in a range of therapeutic areas. Under general supervision, the coordinator identifies eligible patients and ensures research protocols are carried out accurately through assessment, planning, intervention, and evaluation. The role works with physicians, investigators, regulatory staff, and study sponsors to support research processes and reporting.

Skills & qualifications

RequiredNice to have

Skills

Informed ConsentClinical Record ReviewPatient Eligibility AssessmentResearch Protocol ExecutionAdverse Event ReportingElectronic Medical RecordsClinical Trial Management SystemsStudy MonitoringInstitutional Review Board Requirements

Qualifications

Bachelor's Degree2 Years' ExperienceBasic Life Support Certification

Benefits

401(k) Match
Medical Insurance
Dental Insurance
Vision Insurance
Tuition Assistance

Full job description

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 1 will support studies across the Research Department. Therapeutic areas may include pediatric and adult specialties, cystic fibrosis, endocrinology, inpatient research, pulmonology, cardiology, and other areas as department needs evolve.

Under general supervision, the Clinical Research Coordinator 1 is responsible for identifying eligible patients for research and ensuring that research protocols are carried out accurately through assessment, planning, intervention, and evaluation.

  • Under supervision, conducts and documents informed consent process.

  • Reviews clinical records and extracts necessary data to determine eligibility and complete data submission via the appropriate mechanism.

  • Conducts research activities per protocol.

  • Documents research process, adverse event grading, consent process, patient progress on study in electronic medical record.

  • Initiates and submits Serious Adverse Events reports to study sponsor in collaboration with the physician and principal investigator.

  • May maintain clinical trials management system; prepare reports as needed.

  • May prepare for and conduct study monitor visits and audits.

  • Serves as liaison and reference to physicians, investigators and other staff members for questions regarding the research process.

  • Collaborates with investigator and regulatory staff regarding Institutional Review Board requirements.

  • Perform other duties and responsibilities as assigned.

Minimum Qualifications

  • Education: Bachelor’s degree.

  • Experience: 2 years' experience.

  • Licenses/Certifications: Current Basic Life Support (BLS) Provider Certified through American Safety and Health Institute, American Heart Association, or American Red Cross.

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.

How this job compares

Set against the 622 open Clinical Research Coordinator jobs on Olive Jobs, counted October 27, 2026.

Pay
  • This postingNot listed
  • US median$58–75K/yr162 salary ranges
  • US median$24–36/hr177 hourly ranges
Openings
Olive Jobs lists 622 open Clinical Research Coordinator jobs across the US. 2% of them nationwide are listed as remote or flexible.
Hiring the most across the US
Experience
This posting asks for at least 2 years of experience; Clinical Research Coordinator postings that state a minimum ask for 2 years at the median (406 postings).
Education
This posting asks for a bachelor's degree; 203 of the 622 open Clinical Research Coordinator jobs (33%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on October 27, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

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