Entry Level - Clinical Research Coordinators (Non-R.N.) jobs in United States
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University of Utah Health Research · 1 day ago

Entry Level - Clinical Research Coordinators (Non-R.N.)

University of Utah Health Research is seeking Entry Level Clinical Research Coordinators (Non-R.N.) to coordinate day-to-day clinical trial activities. The role involves adhering to Good Clinical Practices, implementing processes within the study team, and working directly with study participants and families.

Higher Education

Responsibilities

Coordinate day-to-day clinical trial activities in adherence to Good Clinical Practices (GCPs), study protocols, and applicable regulations
Implement processes and organize efforts within study team to achieve objectives, coordinating research procedures, study visits, and follow-up care
Create and maintain tools and documentation to track study metrics, providing updates to management
Conduct pre-study, site qualification, study initiation, monitoring visits, and close-out activities
Maintain source documents and report adverse events
Recruit, screen, enroll, and obtain consent from study participants
Collect and maintain patient and laboratory data
Work directly with study participants and families and serve as project liaison to other departments, outside organizations, and government agencies
Work under the direction of the Primary Investigator (PI)
Requires basic skill set and proficiency conducting work assignments as directed by the Clinical Research Manager
May maintain contact with IRB and prepare and submit IRB documents
May ensure proper collection, processing, and shipment of specimens

Qualification

Clinical PracticesClinical trial coordinationPatient interactionOrganizational skillsCommunication skillsProblem-solving skillsTeamwork

Required

Bachelor's degree (or equivalency) + 2 years of directly related work experience or a master's (or equivalency) degree
Active problem-solving skills required
Ability to coordinate day-to-day clinical trial activities in adherence to Good Clinical Practices (GCPs), study protocols, and applicable regulations
Requires basic skill set and proficiency conducting work assignments as directed by the Clinical Research Manager
May maintain contact with IRB and prepare and submit IRB documents
May ensure proper collection, processing, and shipment of specimens
Must fulfill all associated vaccination requirements, or be approved for an exemption, prior to the first day of work

Preferred

Should work well in a team environment (including study staff and clinical operations staff i.e. medical assistants, nurses, etc.)
Successful applicants should have strong communication skills – be comfortable speaking with patients and clinical staff about studies, escalating issues/questions or concerns to management and/or PI's
Ability to read a situation and step in and help as needed within the scope of skillset
Strong organizational and planning skills preferred

Company

University of Utah Health Research

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At University of Utah Health, our world-class researchers work together to tackle some of the toughest problems in health and medicine.

Funding

Current Stage
Late Stage
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