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. In this role, you will perform detailed reviews of
clinical research protocols and utilize 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. Additionally, you will 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. The ideal candidate will
have at a minimum, 1+ years of budget/negotiating experience. 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 $31.51 - $62.64.
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
Oct 31, 2025