University of Arizona
Clinical Research Coordinator II, Department of Internal Medicine – Cardiology (Phoenix)
Phoenix, AZ, US · Mid
Sponsorship not specifiedDetected 1 day ago
Clinical TrialsClinical ResearchResearchCommunicationCollaboration
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Cap-exempt (no lottery)0
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Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70
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About the role
- Recruitment and Enrollment: Conduct study eligibility screening, recruitment, interviews and evaluation of potential study participants per IRB-approved study protocols.
- Coordinate clinical staff education to ensure collaboration on new processes that affect the clinic or hospital operations.
- Compliance and education: Responsible for ensuring compliance with federal regulations for human subject research, University policies, and Sponsor expectations as well as for continuing education relevant to their role.
Responsibilities
- Obtain informed consent, collect and maintain participant data.
- Maintain detailed records of studies conducted, organize and prepare data for input into a variety of internal and external systems.
- Create and file adequate source documentation, ensure timely data reporting and query response, and perform quality checks.
- Collaborate effectively with other departments to ensure proper progress and completion of study procedures.
- Develop strategies to ensure increased study awareness and subject enrollment.
- Supports the orientation and training of new research team members, including faculty, residents/fellows, and other staff.
Requirements
- Ensure participant and study compliance, i.e., collection of study specimens, completion of protocol required tests and completion of study visits within required study visit windows.
- Complete timely collection, labeling, processing, storage, transport and shipping of biological specimens per IATA requirements if required per protocol.
- Order and maintain supplies required for study kits, track spending in this area, and make day-to-day decisions in support of the study.
Skills
- Excellent written and verbal communication skills.
- Ability to multitask with excellent organizational skills.
- Skilled in interacting and working with others; including, peers, patients, management, internal and external stakeholders.
- Ability to work under minimal guidance and use independent judgment to determine best approach.
Benefits
- Develop study recruitment materials and provide patient education regarding study specific requirements and expectations for participation.
- Provide and/or coordinate administration of study treatments, assessments and monitoring of participant health per protocol; ensure participant education concerning protocol responsibilities and maintain ongoing consent.
- Perform scientific and clinical data collection, through patient interaction, clinical observation and electronic health record review in local source and Sponsor EDC platforms.
- Compliance and education:
- Responsible for ensuring compliance with federal regulations for human subject research, University policies, and Sponsor expectations as well as for continuing education relevant to their role.
- Maintaining current human subject research training, attending relevant educational seminars, and professional development in clinical research operations.
Visa & Work Authorization
- Compliance and education: Responsible for ensuring compliance with federal regulations for human subject research, University policies, and Sponsor expectations as well as for continuing education relevant to their role.
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This listing is sourced directly from University of Arizona's careers page and normalized into a canonical job model.