Clinical Research Coordinator IIThe Department of Orthopedics 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 Orthopedics Clinical Research Manager, providing project coordination and support clinical research daily operations. Additionally, the CRC II will ensure successful implementation of and adherence to clinical research protocols and national and local milestones regarding 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, priority setting and serve as a resource for others for all aspects of conducting a clinical trial for complex and multi-center trials. Intermittent off-campus visits may be required. Outstanding U of A benefits include health, dental, and vision insurance plans; life insurance and disability programs; paid vacation, sick leave, and holidays; U of A/ASU/NAU tuition reduction for the employee and qualified family members; retirement plans; access to U of A recreation and cultural activities; and more! The University of Arizona has been recognized for our innovative work-life programs. For more information about working at the University of Arizona and relocations services, please visit the provided link.
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 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. Supports the orientation and training of new research team members, including faculty, residents/fellows, and other staff.
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, and Abilities:
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.
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.
Preferred Qualifications:
Bachelor's in related field of study.
Bilingual in Spanish and English.
Experience in human subjects research.
Flexible schedule to accommodate clinical trial enrollment windows.
FLSA:
ExemptFull Time/Part Time - Full TimeNumber of Hours Worked per Week - 40 Job FTE - 1.0Work Calendar - FiscalJob Category - Research
Benefits:
Eligible - Yes - Full Benefits Rate of Pay - $53,039 - $66,299 Compensation Type - salary at 1.0 full-time equivalency (FTE)
Grade:
7Compensation Guidance - The Rate of Pay Field represents the University of Arizona's good faith and reasonable estimate of the range of possible compensation at the time of posting. The University considers several factors when extending an offer, including but not limited to, the role and associated responsibilities, a candidate's work experience, education/training, key skills, and internal equity. The Grade Range represents a full range of career compensation growth over time. The university offers compensation growth opportunities within its career architecture. To learn more about compensation, please review our Applicant Compensation Guide and our Total Rewards Calculator. Career Stream and Level - PC2Job Family - Clinical Research
Job Function: Research
Type of criminal background check required: Name-based criminal background check (non-security sensitive) Number of Vacancies - 1
