Cancer Center Jobs

Clinical Trial Coordinator

UCLA Jonsson Comprehensive Cancer Center

January 12, 2022
Clinical Trial Coordinator  
Salary: $22.61 - $52.11 hourly  
Job Type: Contract  
Department Name: 1916-CANCER PREVENTION & CNTRL RESEARCH  
Department Website URL: https://ph.ucla.edu/research/centers/center-cancer-prevention-and-control-research  

Job Summary Statement: We seek a highly motivated, dynamic and detail-oriented individual to join our team at the UCLA Center for Cancer Prevention and Control Research (CPCR) and the UCLA Kaiser Permanente Center for Health Equity (CHE) to serve as a clinical research coordinator. Our diverse, multi-disciplinary team includes a collegial group of faculty members, postdoctoral researchers, community experts, full-time staff and graduate students. This individual will coordinate various studies that focus on colorectal cancer screening and prevention, including the FORTE study, which is an NCI-funded study in colorectal cancer prevention looking to determine how often participants who have had 1-2 small benign polyps removed during colonoscopy should have repeat surveillance colonoscopies. The team member will coordinate research activities under the direction of Dr. May and other clinical trial collaborators. The individual will be responsible for identification and enrollment of study participants; longitudinal follow-up of study participants; data collection and monitoring; development and dissemination of patient communication and education materials; regulatory submissions of events as needed; protocol and information dissemination to investigators, health care professionals, patients and family members; and participation in a range of academic health center and community-partnered research projects. The individual will be responsible for timely and accurate data management related to research studies and will ensure protocol procedures have been completed accurately, safely, and in a timely manner under the supervision of the principal investigators. Further, this position requires that the individual adheres to all relevant regulatory and Good Clinical Practice (GCP) guidelines and ensure the timely coordination and completion of study related procedures for which the coordinator is responsible.  
Percentage of Time: 100  
Shift Start: 8:00 am  
Shift End: 5:00 pm  

More information and APPLY HERE