Description
We are seeking a motivated and qualified Regulatory Coordinator to join our team. The successfulcandidate will support regulatory and compliance activities across a robust portfolio ofinvestigational drug and device studies. This role requires strong communication, organizational,problem-solving, and collaborative skills, along with the ability to manage multiple priorities effectively. The ideal candidate will demonstrate professionalism, sound judgment, attention to detail, and astrong commitment to quality and regulatory compliance. This position provides an opportunity tomake a meaningful contribution to the success of clinical research programs while workingcollaboratively with colleagues, investigators, study teams, and other key stakeholders. Hourly Salary Range $33.09- $65.77. Please note, the department's target hourly salary range is: $35.00 - $40.00
Qualifications
Required:
- Bachelor's Degree and/or equivalent combination of education and experience.
- Minimum of 1+ years of experience as a clinical researcher.
- Interpersonal
skills to effectively communicate information in a timely, professional manner
and establish and maintain cooperative and effective working relationships with
students, staff, faculty, external collaborators and administration and to work
as a member of a team. - Ability to set
priorities and complete ongoing tasks with competing deadlines, with frequent
interruptions, to meet the programmatic and department needs, while complying
with applicable University policies and federal and state regulations. - Analytical
skills to assess clinical research protocols and regulatory requirements,
define problems, formulate logical solutions, develop alternative solutions,
make recommendations, and initiate corrective actions. - Close
attention to detail to ensure accuracy in a fast-paced, fluctuating workload
environment. - Organization
skills to create and maintain administrative and regulatory files effectively
as well as independently balance the various tasks to ensure deadlines are met - Demonstrated
proficiency with Adobe and Microsoft suite software, especially Excel, to
perform daily tasks efficiently and accurately. - A learning and
professional growth mentality so that new software tools, systems, and
processes can be adopted quickly and efficiently. - Working
knowledge of clinical research concepts, policies and procedures, and human
safety protection regulations and laws. - Knowledge of
and experience working with a variety of local and external IRBs, scientific
review and other research committees, national cooperative group sponsors,
industry sponsors, federal and foundation funding organizations, etc.
|
University of California - Los Angeles Health
$33.09-65.77 Hourly
Oct 03, 2026