Clinical Research Coordinator II, Department of Internal Medicine (COM-Phoenix)
University of ArizonaAbout the role
The Department of Internal Medicine at The University of Arizona College of Medicine –Phoenix, invites candidates interested in a rapidly growing career as a Clinical Research Coordinator II (CRC II). The selected individual will work under the supervision of the Internal Medicine Manager of Clinical Research, providing project coordination and support for clinical research daily operations. Additionally, the CRC II will ensure successful implementation of, and adherence to, clinical research protocols and national and local milestones for planning, administration, timeline management, enrollment, participant engagement, data collection, and reporting. This individual will also be involved in the clinical research activities of the various Institutes, including the creation and population of databases, and will have close interactions with faculty members leading these research activities. The CRC II will demonstrate competence in clinical research skills, problem-solving, and priority setting, and serve as a resource for others on all aspects of conducting complex, multi-center clinical trials. Intermittent off-campus visits may be required.
This position, which will be located at the Banner University Medical Center-Phoenix, is currently undergoing rapid growth, and the selected individual will be an important driver of this change.
- Visa sponsorship is not available for this position.
The University of Arizona has been recognized for its innovative work-life programs. For more information about working at the University of Arizona and relocation services, please click here.
Duties & ResponsibilitiesRecruitment and Enrollment:
- Conduct study eligibility screening, recruitment, interviews and evaluation of potential study participants per IRB-approved study protocols.
- Obtain informed consent, collect and maintain subject data.
- Develop study recruitment materials and provide patient education regarding study specific requirements and expectations for participation.
- Coordinate clinical staff education to ensure collaboration on new processes that affect the clinic or hospital operations.
Research Coordination:
- Provide administration of study treatments, assessments and monitoring of participant health, participant education concerning protocol responsibilities and ongoing consent.
- Ensure participant and study compliance, i.e. collection of study specimens, and completion of study visits and research procedures within required study windows.
- Complete timely collection, labeling, processing, storage, transport and shipping of biological specimens per IATA requirements.
Data Coordination:
- Perform scientific and clinical data collection, through patient interaction, clinical observation and electronic health record review.
- 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 perform quality checks.
Troubleshooting:
- Collaborate effectively with other departments to ensure proper progress and completion of study procedures.
- Develop strategies to ensure increased study awareness and subject enrollment.
- Order and maintain supplies required for study kits, track spending in this area, and make day-to-day decisions in support of the study.
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 clin
Apply for this role
Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.
Apply Now →Generate Application KitFree account required — sign up in 30s