"Clinical Research Coordinator II, University of Arizona Cancer Center (Multiple)(Full-Time)"

Position Highlights

The University of Arizona Cancer Center (UACC) is a National Cancer Institute-designated Comprehensive Cancer Center committed to preventing and curing cancer through exceptional patient care, groundbreaking research, and comprehensive education. The clinical research coordinator is responsible for consenting, screening and coordinating collection and submission of data, and follow up for all patients on assigned clinical trials. The coordinator serves as the liaison between the regulatory staff, research RNs, clinic staff and physicians and research sponsor to carry out the required events determined by the protocol calendars including data entry. Each coordinator works on Investigator Initiated Trials (IITs), sponsored studies and National Clinical Trial Network studies (NCTN) ranging from phase 1-4 with varying complexities. The coordinator is involved from the time of the site evaluation visit, site initiation visit and start up all the way to study closure. 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! 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 click here.

Duties & Responsibilities

Act as the primary Clinical Research Coordinator for Oncology Clinical Trials: Coordinate the patient care requirements of IRB approved clinical trials protocols. This includes consenting, screening, registering, re-consenting, scheduling appointments and procedures, creating documentation, and submitting data. Works with a team to create plans to confirm proper execution of clinical trial study procedures. Participate in Site Evaluation Visits (SEV), Site Initiation Visits (SIV), monitoring visits and audits for Investigator Initiated trials (IITs), sponsored studies and cooperative group trials. Participate in and Help Create Trainings and Attend Required Staff Meetings: This includes training from the Clinical Trials Office, University of Arizona, Banner and Sponsors to stay informed of processes and procedures. Willing to be trained in phlebotomy and/or vitals collection through our clinical partner. Perform Data Management Tasks: Following ALCOA-C guidelines, all data collected must be attributable, legible, contemporaneous, original and accurate. Gain access to all associated clinical trail data management systems and confirm all necessary staff also have access. Ensures proper data collection and submission of data into the appropriate data management systems including our local clinical trials management system, the electronic medical record system and specific electronic data capture systems. Evaluate tumor response with Response Evaluation Criteria in Solid Tumors (RECIST) and other evaluation criteria used in Oncology. Collect appropriate signatures to stay in compliance with GCP. Follow up on monitoring report action items and queries in a timely manner. Provide Direct Patient Care: Acts as primary coordinator to meet the time points of assigned clinical trial calendars. Instructs and counsels patients and family members in research procedures. This includes assisting with giving report to pharmacy and infusion nurses for clarification on each specific patients status on each protocol. Work with pharmacokinetic coordinators to collect fresh biopsy collection and participate in the processing and shipment of samples when necessary. Maintain Proper Communication Across Study, Clinical and Research Staff: Constant communication is required between clinic staff, research RNs, pharmacokinetic team members, study monitors, physicians and patients. Patients must be regularly informed of their appointments and research specific requirements (example: additional visits for blood draws and other biological specimen submissions). Act as primary contact for all assigned clinical trials for study monitors, physicians and other staff including finance representatives from UArizona and our Clinical Partner. Other tasks as assigned.

Knowledge, Skills, and Abilities

Demonstrated strong interpersonal, communication, and problem-solving skills. Excellent organizational skills. Attention to detail. Ability to multitask using time management skills. Comfortable with navigating electronic databases.

Minimum Qualifications

Bachelor's degree or equivalent advanced learning attained through professional level experience required. Minimum of 3 years of relevant work experience, or equivalent combination of education and work experience.

Preferred Qualifications

Experience working or volunteering directly with patients in a healthcare setting. Knowledge of clinical research, preferably in Oncology.

FLSA

Exempt

Full Time/Part Time

Full Time

Number of Hours Worked per Week

40

Job FTE

1.0

Work Calendar

Fiscal

Job 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

7

Career Stream and Level

PC2

Job Family

Clinical Research

Job Function

Research

Type of criminal background check required

Name-based criminal background check (non-security sensitive)

Number of Vacancies

3

Contact Information for Candidates

Annie Phinizy | aphinizy@arizona.edu

Open Until Filled

Yes

Documents Needed to Apply

Resume and Cover Letter