Job Title: Clinical Research Coordinator II (CRC II)

Work Location: Bannock County & Bonneville County, Idaho

Summary:

The Clinical Research Coordinator is responsible for independently managing all aspects of assigned clinical trials, ensuring compliance with protocols, ethical standards, and regulatory requirements. This mid-level role involves overseeing multiple studies, supporting junior team members, and collaborating with site staff to maintain high-quality trial execution. The position requires travel between two locations within Eastern Idaho.

Responsibilities:

• Independently oversee clinical trial activities, ensuring strict adherence to study protocols and regulatory standards.
• Serve as lead coordinator on assigned studies, managing daily operations and monitoring participant and staff activities.
• Screen and enroll study participants, conduct interviews, review medical records, and perform clinical procedures such as vitals, phlebotomy, lab processing, and EKGs.
• Manage interactions with trial monitors, address compliance queries, and implement necessary corrections.
• Identify and escalate safety concerns, participate in root cause analysis for protocol deviations, and maintain drug accountability records.
• Maintain accurate research documentation, ensure timely data entry and query resolution, and uphold high data quality standards.
• Assist with onboarding and training of new team members, provide guidance to junior staff, and collaborate with site personnel for smooth study operations.
• Coordinate equipment maintenance, manage inventory and supplies, educate patients, process lab specimens, and support administrative tasks as needed.

Qualifications:

• High school diploma or equivalent required.
• Minimum two years of experience as a Clinical Research Coordinator.
• At least two years of experience as a Medical Assistant or completion of a Certified Medical Assistant program.
• Proficiency in performing EKGs, blood collection, obtaining vitals, and documenting medical history.
• Experience serving as lead CRC on at least four studies.
• CCRC certification preferred; must be actively pursuing or have a plan to obtain within 24 months.
• Valid driver’s license and current automobile insurance required.
• Strong written and verbal communication skills, problem-solving abilities, and attention to detail.
• Ability to manage multiple studies independently, prioritize tasks, and maintain professionalism.
• Proficiency with Microsoft Office, Adobe Acrobat, and clinical trial management systems.
• Knowledge of medical terminology, laboratory standards, and regulatory documentation requirements.
• Ability to lift, pull, push, and manipulate equipment and patients; capable of sitting or standing for extended periods and operating a computer.

Published Category: Clinical Operations & Development