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Minneapolis, Minnesota, United States · On-site
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Minneapolis, Minnesota, United States · On-site
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Minneapolis, Minnesota, United States · On-site
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Minneapolis, Minnesota, United States · Remote OK
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Minneapolis, Minnesota, United States · Remote OK
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Minneapolis, Minnesota, United States · On-site
The optometrist will conduct eye exams for Acuity Eyecare group and strive to practice to the full capacity of their license. The optometrist will support practice growth by establishing patient relationships and educati…
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The coordinator manages day-to-day operations of multiple clinical research studies, including patient recruitment and data collection. They serve as the primary liaison between the site investigator, sponsors, and regulatory bodies to ensure protocol compliance.
A Bachelor's degree is required, with a Master's preferred, along with 2-3 years of research assistant experience. Candidates must be US citizens and possess knowledge of Good Clinical Practice and federal research regulations.
Job Title: Clinical Research Coordinator
Location: Minneapolis VA Medical Center
Job Code: CRC, Full-Time, Benefits-Eligible, Exempt
Supervisor: Principal Investigator
Project:
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 Clinical Research Coordinator
Position Description:
The Clinical Research Coordinator is responsible for the day-to-day operations of multiple clinical research studies. This position will actively enroll patients at the Minneapolis VA Medical Center.
Responsibilities: Major duties and responsibilities may include, but are not limited to the following:
• Maintain close communication with local and network study leadership and staff.
• Manage the study start-up process, including finalization of Informed Consent Forms
and preparation of study start-up materials.
• Collaborate with the central Institutional Review Board overseeing VA sites, and the
local Research and Development Committee (RDC), to ensure that regulatory
requirements at the local site are identified, communicated, and observed.
• Oversee enrollment and study activities with the Site Investigator.
• Recruit participants, collect data in accordance with established study procedures,
follow up with participants in a timely manner.
• Dispense and track investigational study drug per protocol and in keeping with safe
medication handling practices.
• Conduct phlebotomy and urine sample collection per study protocol.
• Coordinate home visits between contract Home Health Service and study participants.
• Monitor subjects' progress, including documentation and reporting of adverse events.
• Ensure staff and subject compliance with protocol guidelines and requirements of
regulatory agencies.
• Implement protocols to ensure data is collected in a scientifically valid manner.
Responsible for alerting the Site Investigator of data collection/protocol breeches,
inconsistencies, or other problems that may arise within the study, as well as suggesting
methods of correction. Maintain data and study files in accordance with study protocols.
• Serve as primary liaison with Site Investigator, staff, internal/external resources and
sponsor regarding patient care issues and progress of the study.
• Maintain local budgets for the study; regularly report progress on all aspects of the
project to the Site Investigator.
• Prepare documentation to support billing for this study’s sub-award, in cooperation
with CVRE staff.
• Track expected and annual payments from the sponsor, in cooperation with CVRE staff.
• Ensure that study activities are completed in an ethical, culturally responsive,
scientifically rigorous, and timely manner in accordance with principles of Good Clinical
• Other duties as assigned
Applicant must include a cover letter
Minimum Qualifications:
Education: Bachelor’s Degree required (Master’s preferred)
Experience: 2-3 years of Research Assistant experience
0-2 years of Coordinator experience required for CRC I
2-4 years of Coordinator experience required for CRC II
Preferred working knowledge of the study
Licensure/Registration/Certification: None
Knowledge, Skills, and Abilities:
Conditions of Employment:
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.
CVRE is a VA-affiliated nonprofit organization organized to support research and education at the Minneapolis VAHCS.
Welcome to the Center for Veterans Research and Education (CVRE) CVRE was established in 1988 to conduct, promote and support the medical research and education activities of the Minneapolis VA Healthcare System and to advance the well being of veterans and the general public by these endeavors. CVRE is a 501(c)(3) non-profit, tax-exempt institute. Collaborative endeavors may be established with universities, for profit companies, hospitals, charitable foundations, professional societies, the NIH, Department of Defense, or other governmental agencies, and other non-profit entities. CVRE supports research in the following key areas: • Psychology • Cardiovascular Health • Metabolism/Diabetes • Respiratory Disease/Pulmonology • Neuroscience •Infectious Diseases • Ophthalmology • Oncology/Cancer • Outcomes Research & Informatics • Orthopedics and Physical Medicine Specific areas of interest include Post Traumatic Stress Disorder, Behavioral Neurosciences, Addictions, the origins of the Gulf War Syndrome, the Neurophysiology of Mental Illness, Traumatic Brain Injury and leading edge research and innovations in Prosthetics and Artificial Limbs.
Offices: 1 Veterans Dr, Minneapolis, Minnesota 55417, US
View all jobs at Center for Veterans Research and EducationThere are currently 495 open science & research positions in Minneapolis, MN listed on Clera. New openings are added daily as companies post roles.
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