OverviewYou can find the cures you know are out there.
At UCLA Health, you make it happen as part of a groundbreaking Research team, working to understand hundreds of medical disorders and improving processes for dozens of procedures across the globe.Job DutiesResponsibilities Under the supervision of the Principal Investigators (PI) serve as Research Study Coordinator.
Conduct and have primary responsibility for the operations of research trial protocols and enroll trial subjects within the Division of Digestive Diseases.
Responsibilities include coordination and management of recruiting, interviewing, evaluating, and determining eligibility of study candidates for research participation; maintaining subject relationships to enhance subject trial retention; performing protocol-based data collection and reporting, including adequate documentation of informed consent and adverse events.The Coordinator is the key person to overseeing the research process from inception to completion.
Participate in long-term planning and day-to-day management of several research projects while maintaining all regulatory documents.
In addition, ensure the safety and protection of human subjects, maintains integrity of research efforts consistent with IRB research protocols, trains, processes, and manages large team of student/trainee research volunteers, plans and coordinates research meetings, serves as the administrative liaison for multi-center collaborations where UCLA is either the data coordinating center or lead institution.
Prepare all documentation for Institutional Review Board (IRB) approvals.UCLA is an Equal Opportunity/Affirmative Action employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected Veteran status.Job QualificationsQualificationsRequired: Ability and experience to manage and run multiple clinical trials concurrently.
Familiarity with federal regulatory standards relating to human subjects research, FDA and NIH Familiarity with clinical trial protocol development.
Experience in IRB applications and informed consent.
Appreciation of the needs to enroll and close studies on schedule Ability to organize and present data in spreadsheets.
Ability to deal with complex interpersonal situations with equanimity.
Knowledge of staff certification requirements for clinical trials (human subjects training, laboratory, radiation and biohazard safety, IATA shipping, etc).
Ability to have transportation throughout LA area to all UCLA Health sites as needed for projects.
nnby Jobblenn