Job Title: Clinical Research Coordinator II (CRC II)

Work Location: Ada County, Idaho

Summary:

The Clinical Research Coordinator II (CRC II) 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 leading studies, supporting junior staff, and collaborating with site teams to maintain high-quality trial execution, particularly in cardiology and nephrology research.

Responsibilities:

• Independently oversee clinical trial operations, ensuring adherence to study protocols, regulatory standards, and ethical guidelines.
• Lead assigned studies, manage daily activities, and monitor participant and research staff compliance.
• Screen and enroll study participants, conduct interviews, review medical records, and perform clinical procedures such as vitals, phlebotomy, lab processing, and EKGs.
• Maintain accurate research documentation, manage data entry and query resolution, and ensure timely transmission of clinical data.
• Identify, escalate, and contribute to the resolution of safety issues and protocol deviations.
• Provide guidance and support to junior CRC staff, assist with onboarding, and collaborate with site teams for study execution.
• Manage site logistics including equipment maintenance, supply inventory, and laboratory specimen processing and shipping.
• Support administrative tasks such as scheduling, patient education, and maintaining confidentiality of sensitive information.

Qualifications:

• High school diploma or equivalent required.
• Minimum of 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 (cumulative).
• CCRC certification preferred; must be actively pursuing or have a plan to obtain within 24 months.
• Strong written and oral communication skills, problem-solving abilities, and attention to detail.
• Ability to manage multiple studies independently and provide technical guidance to junior staff.
• Knowledge of medical terminology, laboratory standards, and clinical trial management systems.
• Valid driver’s license and current automobile insurance.
• Physical ability to lift, push, pull, and manipulate equipment and patients; ability to sit or stand for extended periods and operate a computer.

Published Category: Clinical Operations & Development