Clinical Research Coordinator II, Department of Internal Medicine (COM-Phoenix)

Clinical Research Coordinator II, Department of Internal Medicine (COM-Phoenix) 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. Position Highlights Visa sponsorship is not available for this position. Outstanding U of A benefits include health, dental, and vision insurance plans; life insurance and disability programs; paid vacation, sick leave, and holidays; UA/ASU/NAU tuition reduction for the employee and qualified family members; state retirement plan; access to UA recreation and cultural activities; and more! Duties & Responsibilities Recruitment 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 clinical research operations. Supports the orientation and training of new research team members, including faculty, residents/fellows, and other staff. Knowledge, Skills & Abilities Phlebotomy certified. Ability to multitask with excellent organizational skills. Excellent written and verbal communication 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. Minimum Qualifications Bachelor's degree or equivalent advanced learning attained through professional level experience required. Three (3) years of relevant work experience, or equivalent combination of education and work experience. Employment Information Location: Greater Phoenix Area Contract type: Full Time Number of Hours Worked per Week: 40 Work Calendar: Fiscal Rate of Pay: $53,039-$66,299 FLSA: Exempt Background Check Type of criminal background check required: Name-based criminal background check (non-security sensitive) Contact Information Office of Talent Acquisition View email address on click.appcast.io Additional Information Notice of Availability of the Annual Security and Fire Safety Report: In compliance with the Jeanne Clery Campus Safety Act (Clery Act), each year the University of Arizona releases an Annual Security Report (ASR) for each of the University's campuses. These reports disclose information including Clery crime statistics for the previous three calendar years and policies, procedures, and programs the University uses to keep students and employees safe, including how to report crimes or other emergencies and resources for crime victims. As a campus with residential housing facilities, the Main Campus ASR also includes a combined Annual Fire Safety report with information on fire statistics and fire safety systems, policies, and procedures. Paper copies of the Reports can be obtained by contacting the University Compliance Office at View email address on click.appcast.io. #J-18808-Ljbffr Phase2 Technology