Arizona Veterans Research and Education Foundation
Clinical Research Coordinator (CRC)
Arizona Veterans Research and Education Foundation, Phoenix, Arizona, United States, 85012
Job Description
Job Description
Position Title:
Clinical Research Coordinator (CRC) Location:
Arizona Veterans Research and Education Foundation is based on the Phoenix VA Medical Center Campus in Phoenix, Arizona. We also have a downtown laboratory in the Bioscience Center (UofA building). Schedule:
Full-time (40 hours/week) Minimum Contract Obligations:
1 year, grant funded Salary:
Commensurate with experience and qualifications; range $49,000 to $73,000
Join a great team working with our military veterans! We are a non-profit medical research organization based in Phoenix, Arizona. At Arizona Veterans Research and Education Foundation (AVREF), we offer our team members the opportunity to work on impactful research that benefits veterans’ health, while enjoying a competitive salary, generous benefits, a collaborative environment, and flexible scheduling. About Us: Arizona Veterans Research and Education Foundation (AVREF) uniquely partners with the Phoenix Veterans Administration Health Services, universities, and pharmaceutical/ device companies to conduct research benefiting military veterans. Our Research makes a difference! We bring cutting-edge research opportunities to veterans, improving their lives. The Position: We’re looking for a Clinical Research Coordinator (CRC). The CRC will recruit, screen, and enroll eligible participants, implement protocol procedures, monitor follow-up visits, and oversee regulatory and administrative details as needed. The salary range reflects industry standards, and we offer a robust benefits package, including health, vision, and dental insurance, life insurance, short and long-term disability benefits, a Simple IRA with matching funds (immediate vesting), vacation, and sick leave. This position is contingent upon approval from the Veterans Affairs Administration and may be rescinded if approval is not granted. Approval can take anywhere from 2-4 months. Position start date will be given once approval is acquired. Study Types: We are recruiting CRCs to work as part of a team on research projects investigating pain management, nutrition, and other interventions to improve veterans’ health. The studies are stable, funded, and ongoing. Flexibility to work on several studies, either independently or as part of a team, is essential. Requirements: Prior successful clinical research experience Knowledge of medical terminology Excellent understanding of project management and clinical research processes Willingness to cross-train in other roles as needed Detail-oriented, self-directed, and able to work within a team environment Personable, collaborative, and cooperative Comfortable with or willing to learn minimally invasive medical procedures Ability to pass a background check Proficient in technology: email, Microsoft Office, teleconferencing, and Electronic Medical Record (EMR) systems Ability to draw blood and process laboratory samples Know how to analyze, collect, and store data from EMR Eligible for VA Appointment (WOC or IPA). Preferred: Medical background ACRP or CCRP certification Bachelor’s degree or higher Safety Pac, BLS and CITI Responsibilities: Daily administration and conduct of research projects Interact with Principal Investigators, Sub-Investigators, Research Committee Coordinators, laboratory staff, and clinical staff from various departments Provide direct coordinator
services/procedures/consultation
and participate in site visit activities from a sponsor or granting agency Supervise the healthcare of research participants Work with other team members to recruit study participants Complete study visits activities as required by protocol Coordinate study activities with other study sites and central laboratories Assist in the preparation of the study, review documents, and correspondence with the Research Committees Screen, recruit, and enroll qualified subjects into clinical trials and monitor their status Comply with all SOPs, regulations, and good clinical and ethical practices Ensure accurate clinical assessment, source documentation, data collection, regulatory file composition, and trial communications with subjects, investigators, and caregivers Prepare and submit trial-specific information to the IRB and others, as assigned Benefits: Simple IRA with matching funds (immediate vesting) Dental Insurance Health insurance Vision insurance Life insurance, short and long-term disability benefits Sick leave and vacation time
Job Description
Position Title:
Clinical Research Coordinator (CRC) Location:
Arizona Veterans Research and Education Foundation is based on the Phoenix VA Medical Center Campus in Phoenix, Arizona. We also have a downtown laboratory in the Bioscience Center (UofA building). Schedule:
Full-time (40 hours/week) Minimum Contract Obligations:
1 year, grant funded Salary:
Commensurate with experience and qualifications; range $49,000 to $73,000
Join a great team working with our military veterans! We are a non-profit medical research organization based in Phoenix, Arizona. At Arizona Veterans Research and Education Foundation (AVREF), we offer our team members the opportunity to work on impactful research that benefits veterans’ health, while enjoying a competitive salary, generous benefits, a collaborative environment, and flexible scheduling. About Us: Arizona Veterans Research and Education Foundation (AVREF) uniquely partners with the Phoenix Veterans Administration Health Services, universities, and pharmaceutical/ device companies to conduct research benefiting military veterans. Our Research makes a difference! We bring cutting-edge research opportunities to veterans, improving their lives. The Position: We’re looking for a Clinical Research Coordinator (CRC). The CRC will recruit, screen, and enroll eligible participants, implement protocol procedures, monitor follow-up visits, and oversee regulatory and administrative details as needed. The salary range reflects industry standards, and we offer a robust benefits package, including health, vision, and dental insurance, life insurance, short and long-term disability benefits, a Simple IRA with matching funds (immediate vesting), vacation, and sick leave. This position is contingent upon approval from the Veterans Affairs Administration and may be rescinded if approval is not granted. Approval can take anywhere from 2-4 months. Position start date will be given once approval is acquired. Study Types: We are recruiting CRCs to work as part of a team on research projects investigating pain management, nutrition, and other interventions to improve veterans’ health. The studies are stable, funded, and ongoing. Flexibility to work on several studies, either independently or as part of a team, is essential. Requirements: Prior successful clinical research experience Knowledge of medical terminology Excellent understanding of project management and clinical research processes Willingness to cross-train in other roles as needed Detail-oriented, self-directed, and able to work within a team environment Personable, collaborative, and cooperative Comfortable with or willing to learn minimally invasive medical procedures Ability to pass a background check Proficient in technology: email, Microsoft Office, teleconferencing, and Electronic Medical Record (EMR) systems Ability to draw blood and process laboratory samples Know how to analyze, collect, and store data from EMR Eligible for VA Appointment (WOC or IPA). Preferred: Medical background ACRP or CCRP certification Bachelor’s degree or higher Safety Pac, BLS and CITI Responsibilities: Daily administration and conduct of research projects Interact with Principal Investigators, Sub-Investigators, Research Committee Coordinators, laboratory staff, and clinical staff from various departments Provide direct coordinator
services/procedures/consultation
and participate in site visit activities from a sponsor or granting agency Supervise the healthcare of research participants Work with other team members to recruit study participants Complete study visits activities as required by protocol Coordinate study activities with other study sites and central laboratories Assist in the preparation of the study, review documents, and correspondence with the Research Committees Screen, recruit, and enroll qualified subjects into clinical trials and monitor their status Comply with all SOPs, regulations, and good clinical and ethical practices Ensure accurate clinical assessment, source documentation, data collection, regulatory file composition, and trial communications with subjects, investigators, and caregivers Prepare and submit trial-specific information to the IRB and others, as assigned Benefits: Simple IRA with matching funds (immediate vesting) Dental Insurance Health insurance Vision insurance Life insurance, short and long-term disability benefits Sick leave and vacation time