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Clinical Research Coordinator Clinical - MILWAUKEE, WI,

Job Information

Job Order ID :
WI3834614
# of Positions :
1
Minimum Education Level :
High School Diploma/GED
Experience Required :
Training :
High School Diploma/GED Equivalent
Duration :
Shift :
Unspecified
Hours per week:
40

Job Description

 
JOB REQUIREMENTS: Clinical Research Coordinator - Clinical Trials &
Research Office Job Locations US-WI-Wauwatosa ID 2025-11419 Category
Research and Development Position Type Full Time Overview Located in
Milwaukee, Wisconsin, the Versiti Blood Research Institute (VBRI) is the
largest blood-focused research institute in the United States. With over
30 basic, translational, and clinical investigators, the institute is
dedicated to advancing scientific knowledge and developing innovative
therapies related to blood and blood disorders. The institute\'s
research interests encompass a wide range of topics, including
transfusion medicine, cellular therapy, thrombosis/hemostasis,
immunology, and hematologic malignancies. As a vital part of Versiti, a
non-profit organization with a blood bank at its core, the VBRI strives
to improve lives through innovative research and the development of
novel diagnostics and treatments. VBRI is part of the Milwaukee Regional
Medical Campus, a rapidly growing clinical-translational research hub.
VBRI\'s proximity to the Medical College of Wisconsin, Childrens\'
Hospital of Wisconsin, and Froedtert Hospital facilitates seamless
interdisciplinary collaborations. A range of exemplary core facilities
support highly competitive research. In the summer of 2024, construction
of a new research building began, doubling existing VBRI research space
to enable the recruitment of 10-15 new faculty. With its renowned
researchers, strategic expansion plans and location in a highly
collaborative environment, the VBRI is poised to maintain and expand its
position as one of the leading hematology institutes in the world.
Position Summary Under the direction of the Principal Investigators
(PIs) and CTRO Supervisor, is responsible for coordinating research
trials from initiation to completion in compliance with regulations and
requirements. Assists in the management of trial budgets and implements
and oversees systems to manage the conduct of the clinical trials and
the flow of information among stakeholders. Total Rewards Package
Benefits Versiti provides a comprehensive benefits package based on your
job classification. Full-time regular employes are eligible for Medical,
Dental, and Vision Plans, Paid Time Off (PTO) and Holidays, Short- and
Long-term disability, life insurance, 7% match dollar for dollar 401(k),
voluntary programs, discount programs, others. Responsibilities Subject
Interaction: \* Obtains consent and enrolls study subjects \*
Communicates with study subjects, ensuring they receive applicable
information. May include training and\... For full info follow
application link. We embrace and encourage diversity in our workforce.
Equal Opportunity Employer of Minorities, Females, Protected Veterans,
and Individuals with Disabilities. We participate in eVerify. We
maintain a drug-free workplace and perform pre-employment substance
abuse testing. We are a tobacco/smoke-free workplace. \*\*\*\*\*
APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/29E5364523834E6B
Qualified females, minorities, and special disabled veterans and other
veterans are encouraged to apply.

Company Information

Name :
BLOODCENTER OF WISCONSIN, INC

Application Information

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