Clinical Research Coordinator II, Department of Internal Medicine (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 Senior Director of Clinical Research Operations, 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. 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

Outstanding UA 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; retirement plans; access to UA recreation and cultural activities; and more!

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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.

• Bachelor's degree in related field of study 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.

• Bilingual in Spanish and English.
• Experience in human subjects research.
• Flexible schedule to accommodate clinical trial enrollment windows.

• Application: The online application should be completed in its entirety. Blank or missed information may be considered an incomplete submission.
• Cover Letter: Should clearly indicate how your skills and professional employment experience meet the Minimum and the Preferred qualifications (if applicable).