WI3833237

1

High School Diploma/GED

High School Diploma/GED Equivalent

Unspecified

40

JOB REQUIREMENTS: Senior Clinical Research Coordinator Job Locations
US-WI-Wauwatosa ID 2024-10978 Category Research and Development Position
Type Full Time Overview Versiti is a fusion of donors, scientific
curiosity, and precision medicine that recognize the gifts of blood and
life are precious. We are home to the world-renowned Blood Research
Institute, we enable life saving gifts from our donors, and provide the
science behind the medicine through our diagnostic laboratories. Versiti
brings together outstanding minds with unparalleled experience in
transfusion medicine, transplantation, stem cells and cellular
therapies, oncology and genomics, diagnostic lab services, and medical
and scientific expertise. This combination of skill and knowledge
results in improved patient outcomes, higher quality services and
reduced cost of care for hospitals, blood centers, hospital systems,
research and educational institutions, and other health care providers.
At Versiti, we are passionate about improving the lives of patients and
helping our healthcare partners thrive. 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. Manages
trial budgets and implements and oversees systems to manage the conduct
of the clinical trials and the flow of information among stakeholders.
May serve as a team lead or experienced coordinator mentor. May lead a
disease function research area. 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 education regarding the study. \*
Serves as a liaison between study subjects and Principal
Investigator/research team to provide proactive communication. \* May
collect samples from subjects as applicable/assigned. Stakeholder
Interaction: \* Serves as a liaison with stakeholders including members
of the research team, IRB (Institutional Review Board), study sponsors,
hospitals/hospital staff, BCW staff, national data coordinating centers,
and granting agencies. 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/8CD1E8758C4F4B8F
Qualified females, minorities, and special disabled veterans and other
veterans are encouraged to apply.