Research Study Coordinator
Job Title: RESEARCH STUDY COORDINATOR
Location: Minneapolis VA Medical Center
Job Code: Research Study Coordinator, Full Time, Benefit Eligible, Exempt
Summary:
The Center for Veterans Research and Education (CVRE), whose mission is helping to support
innovative research and education initiatives that improve the health and well-being of Veterans, is
seeking a Research Study Coordinator.
Position Description:
The Research Study Coordinator will support investigators and other personnel within the Minneapolis
Adaptive Design and Engineering (MADE) Program at the Minneapolis VA Health Care System. Projects
in the MADE Program include research, development, and evaluation of technologies and therapies
intended to improve the lives of Veterans. Example projects include design of wheelchairs, prostheses,
exercise equipment, footwear, and mobile applications.
Responsibilities:
Major duties and responsibilities include, but are not limited to the following:
• Support the coordination and management of all aspects of multiple MADE research
projects:
o Assist with subject recruitment, screening, consent, and enrollment.
o Schedule and facilitate meetings and study visits, including the set-up of necessary
equipment.
o Perform study data collection and entry.
• Monitor implementation, management, coordination and documentation of all study
activities.
• Ensure that project components are completed in an ethical, scientifically rigorous, and
timely manner.
• Ensure compliance with safety regulations and that lab specific protocols are established
and followed.
• Continuously update safety records and procedures.
• Provide administrative support to initiate studies including assisting with preparation of
grant applications and Institutional Review Board (IRB) submissions.
• Acquire internal approvals, documentation, and regulation management.
• Participate in regular meetings reporting progress and/or problems encountered in the
conduct of the study.
• Prepare a variety of documents such as memos, reports, briefing materials, etc., in final
form, including drafting, editing, proofreading, and formatting.
• Manage, organize, and coordinate administrative aspects of the MADE Program, including
but not limited to making travel arrangements and preparing vouchers; submitting work
orders/maintenance requests; ordering supplies and maintaining inventory; monitoring
project finances and budgets; scheduling of rooms and conference calls.
• Communicate with Principal Investigator(s) and study team on a regular basis.
• Perform all other related duties as assigned.
APPLICANT MUST INCLUDE A COVER LETTER
Minimum Qualifications:
Education: Bachelor’s (BA/BS) or above from an accredited college or university
Experience: Prior research experience is preferred, including data collection and data
storage, human subjects studies, and IRB processes
Licensure/Registration/Certification: None
Knowledge, Skills and Abilities:
• Basic experience with trouble-shooting devices and software settings.
• Experience in coordinating multiple task and project elements with differing timelines and
completion deadlines.
• Familiarity with REDCap is preferred.
• Demonstrated ability to work effectively both independently and as part of a team.
• Excellent oral and written communication skills.
• Exceptional attention to detail and organizational skills.
• Proficiency in Microsoft Office products including Outlook, Word, PowerPoint and Excel.
Conditions of Employment:
• Subject to a criminal and educational background check.
• Designated and/or random drug testing may be required.
• Regular and predictable attendance is required.
• Typical hours fall within standard business hours, work may be required during hours
beyond standard business hours, including weekends.
• Must be a US citizen
Physical Requirements: The employee must be able to navigate the medical center, use a
keyboard, and life up to 25 lbs. Reasonable accommodation may be considered in determining an
applicant’s ability to perform the duties/functions of the position.