Cognitive Research Coordinator

Location:

Twin Cities Contract Type:
Full-Time About the Job

Work Schedule:

In-person, work hours vary (typically 9am - 5pm with occasional evenings), Mon-Fri with occasional weekends.

• Contribute to study start-up activities, including site initiation visits, OnCore set-up, document template and flow sheet creation, study staff training and clinical in-services.
• Patient recruitment, screening, consent, enrollment, and necessary registrations.
• Independently perform study testing.
• Perform study data collection and entry; collect enrollment and treatment data, using charts, correspondence, electronic medical records, and personal communications with other healthcare workers.
• Independently perform protocol procedures and specimen collection and processing.
• Coordinate/conduct quality control checks as related to study conduct.
• Manage maintenance of subject research charts.
• Coordinate study close-out activities.

• Responsible for the interpretation of, application of, and compliance with federal regulations, Good Clinical Practice (GCP), and University and Clinical Partner policies as they relate to assigned research protocols.
• Under supervision of MnDRIVE and Psychiatry Regulatory Specialist, create and manage regulatory files for new studies.
• Completes IRB and other required review committee applications on assigned protocols.
• Drafts study-related subject informed consent form documents according to Sponsor and University requirements.
• Drafts study-related correspondence, including preparing FDA submissions, for study PI.
• Under supervision of MnDRIVE Regulatory Specialist, creates and maintains all required documents for assigned regulatory binders.
• Assist PIs, Regulatory Specialist, Core Project Manager in preparation for audits/monitoring visits.

• Independently manage and maintain data, data collection, data entry, and appropriate data storage for multiple projects.
• Creates REDCap databases and enters study data.

• Plan and participate local and regional outreach activities aimed at promoting awareness of MnDRIVE research study portfolio.

Other duties as assigned (10%)

All required qualifications must be included in the application materials

Required Qualifications:

• BA/BS with at least two (2) years of experience or a combination of related education and work experience to equal at least 6 years of relevant experience.
• Experience in the preparation of IRB applications.
• Working knowledge of regulations governing research activities (such as GCPs, FDA regulations and ICH guidelines).
• Demonstrates ability to initiate and process multiple projects simultaneously.
• Experience with Office Suite, Google Apps, and web-based systems for tracking activities, calendaring, and retrieving/updating information.
• Possess excellent communication skills; verbal and written.
• Demonstrated ability to provide excellent customer service to internal and external clients.

Preferred Qualifications:

• Minimum of one (1) year experience in clinical research setting in an academic health center.
• Certification as a clinical research professional with SoCRA or ACRP or willingness to obtain certification at time of eligibility.
• EPIC experience.
• MATLAB experience.
• EEG/DBS/MEG/fMRI experience.
• Human psychophysics experience.

To learn more about the Herman Darrow Human Neuroscience Lab, please visit

Pay Range: $24.69/hr - $29.81/hr; depending on education/qualifications/experience

Time Appointment: 100% Appointment

Position Type: Civil-Service & Non-Faculty Labor Represented Staff

Please visit the Office of Human Resources website for more information regarding benefit…