Clinical Research Coordinator - Impactful Trials

Paylocity; Edina (MN); On-site; USD 55,000 - 75,000; Full time

Job summary

Nura is seeking a Clinical Research Coordinator to perform day-to-day activities supporting clinical research under the direction of the Principal Investigator. The role focuses on participant safety, data quality, and protocol compliance across multiple studies.

Responsibilities include coordinating protocols, screening and enrolling participants, collecting data, and ensuring IRB and regulatory compliance. Strong communication and collaboration with research teams are essential.

Qualifications

• Proven ability to communicate effectively in writing and verbally.
• Proficiency with MS Office and data collection tools.
• Experience in clinical research and patient care preferred.

Responsibilities

• Coordinate research protocols and appointments with study teams and sponsors.
• Screen, recruit, consent, and enroll participants per protocol.
• Collect data and complete case report forms in the EDC; monitor events.

Skills

Communication skills

Attention to detail

Team collaboration

Problem solving

Education

Bachelor's degree in a relevant field

Clinical degree with experience

RN desirable

Tools

Microsoft Office Suite

Job description

Nura is seeking a Clinical Research Coordinator to perform day-to-day activities supporting clinical research under the direction of the Principal Investigator. The role focuses on participant safety, data quality, and protocol compliance across multiple studies.

Responsibilities include coordinating protocols, screening and enrolling participants, collecting data, and ensuring IRB and regulatory compliance. Strong communication and collaboration with research teams are essential.