Clinical Research Assistant, Aegis Consortium

at  University of Arizona

KNOWLEDGE, SKILLS, AND ABILITIES (KSAS):

• Detail oriented with excellent organizational skills.
• Ability to communicate effectively with different groups/individuals.
• Ability to handle confidential and sensitive information.
• Strong problem-solving abilities, dependability, and a proactive approach.

MINIMUM QUALIFICATIONS

• High school diploma or equivalent, or equivalent learning attained through experience required.
• Five (5) years of relevant experience, or equivalent combination of education and work experience.

DIVERSITY STATEMENT

At the University of Arizona, we value our inclusive climate because we know that diversity in experiences and perspectives is vital to advancing innovation, critical thinking, solving complex problems, and creating an inclusive academic community. As a Hispanic-serving institution, we translate these values into action by seeking individuals who have experience and expertise working with diverse students, colleagues, and constituencies. Because we seek a workforce with a wide range of perspectives and experiences, we provide equal employment opportunities to applicants and employees without regard to race, color, religion, sex, national origin, age, disability, veteran status, sexual orientation, gender identity, or genetic information. As an Employer of National Service, we also welcome alumni of AmeriCorps, Peace Corps, and other national service programs and others who will help us advance our Inclusive Excellence initiative aimed at creating a university that values student, staff and faculty engagement in addressing issues of diversity and inclusiveness.

• Sending appointment reminders and instructions to research participants for all Tucson-based study procedures for the RECOVER observational study.
• Create and maintain open lines of communication between research coordinators and study participants. This includes making daily phone calls, sending emails, and following up with non-responsive participants.
• Work closely with Clinical Coordinators and Principal Investigators to learn and begin performing the full scope of clinical research coordinator duties.
• Perform a variety of research coordination tasks, such as obtaining informed consent from study participants; collecting, entering, and analyzing subject data; and compiling reports.
• Collect and analyze data adhering to proper research protocols. Prepare documentation, reports, graphs, and other materials.
• Assist in the preparation of documentation, reports, graphs, and other materials, keeping appropriate logs, tracking participants, and preparing study materials.
• Other administrative tasks as assigned.