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

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

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

Posting Number req
26680

Department COM Phx Internal Medicine

Department Website Link https://medicine.arizona.edu/

Location Greater Phoenix Area

Address Banner University Medical Group, 1111 East McDowell Rd., Phoenix, AZ 85006 USA

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 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.

• 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!

• 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.

• 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.

• 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.

• 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…