Clinical Research Coordinator I – Impactful Trials & Growth

St Luke; Boise (ID); Sur place; USD 52 000 - 76 000; Plein temps

Avantages offerts par ce poste

On-site massages

Employee Assistance Program

Personify Health Wellness tool

Formal training and career development

Résumé du poste

St. Luke’s invites applications for the Clinical Research Coordinator 1 role in our Idaho research program.

The coordinator will work under supervision to identify eligible patients, obtain informed consent, and ensure accurate protocol implementation across pediatric and adult studies. Responsibilities include data extraction from records, adverse event documentation, and collaboration with physicians and IRB requirements.

Qualifications

• Requires 2 years of experience in clinical research.
• Current Basic Life Support (BLS) certification.

Responsabilités

• Identify eligible patients for studies and ensure protocol adherence.
• Conduct informed consent processes and document accordingly.
• Review clinical records and extract data to determine eligibility and submit data.
• Carry out study activities per protocol and monitor patient progress.
• Document research processes, adverse event grading, consent, and study progress in EHR.
• Submit Serious Adverse Events reports to the sponsor with physician collaboration.
• May maintain the clinical trials management system and prepare reports.

Description du poste

St. Luke’s invites applications for the Clinical Research Coordinator 1 role in our Idaho research program.

The coordinator will work under supervision to identify eligible patients, obtain informed consent, and ensure accurate protocol implementation across pediatric and adult studies. Responsibilities include data extraction from records, adverse event documentation, and collaboration with physicians and IRB requirements.