Neuroscience Clinical Research Coordinator

University of Minnesota; Minneapolis (MN); On-site; USD 33,000 - 41,000; Full time

Benefits offered by this job

Competitive wages

Tuition benefit

Retirement plans

PSLF opportunity

Employee assistance program

Job summary

University of Minnesota seeks a Clinical Research Coordinator to support a multidisciplinary neuroscience research portfolio. The role covers start-up activities, patient recruitment, data collection, and regulatory compliance in a dynamic academic setting.

The position emphasizes IRB preparation, GCP/FDA regulation adherence, and collaboration with PIs and regulatory staff to ensure high-quality research conduct. In-person work with diverse responsibilities and potential for audits.

Qualifications

• BA/BS with at least two years of experience or equivalent to six years of relevant work.
• Experience in preparing IRB applications.
• Familiarity with regulations governing research (GCP, FDA, ICH).
• Ability to initiate and manage multiple projects simultaneously.
• Proficient with Office Suite, Google Apps, and web-based tracking systems.
• Excellent verbal and written communication; strong customer service.

Responsibilities

• Coordinate study start-up activities including site initiation visits and OnCore setup.
• Recruit, screen, consent, enroll participants and complete necessary registrations.
• Perform study testing and data collection, entry, and storage across projects.
• Prepare protocol procedures, specimen collection/processing, and regulatory binders.
• Support audits/monitoring visits and regulatory submissions as needed.
• Coordinate study close-out activities and regulatory documentation.

Skills

IRB applications

GCP regulations

Multitasking

Office Suite

Communication skills

Education

BA/BS or higher

Tools

EPIC

MATLAB

EEG/DBS/MEG/fMRI

Job description

University of Minnesota seeks a Clinical Research Coordinator to support a multidisciplinary neuroscience research portfolio. The role covers start-up activities, patient recruitment, data collection, and regulatory compliance in a dynamic academic setting.

The position emphasizes IRB preparation, GCP/FDA regulation adherence, and collaboration with PIs and regulatory staff to ensure high-quality research conduct. In-person work with diverse responsibilities and potential for audits.