Description
UCLA HEALTH
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Description
We are seeking an
experienced Budget 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 qualifications, relevant experience, and internal equity
considerations.
Hourly Salary Range: $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.
Preferred:
- Bachelor’s degree