Description
We are seeking an experiencedBudget
Amendment Negotiator who will be responsible for regulatory coordination of
clinical research studies within assigned units, departments, or divisions.
Perform detailed review of clinical research protocols and utilizes that
information to prepare, manage and submit all required study/regulatory
documents and all required applications and forms related to internal UCLA
requirements, FDA requirements, sponsor requirements, etc. Work with study
monitors to process, review and collect the appropriate regulatory documents in
a timely manner and in compliance with federal, state, and university mandated
laws, regulations and policies. Salary offers are determined based on various
factors including, but not limited to, qualifications, experience, and equity.
UCLA Health hourly salary range for this position is $30.56 - $60.82.
Qualifications
Required:
- 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.
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University of California - Los Angeles Health
Apr 19, 2025