Budget Amendment Negotiator - Hematology/Oncology (Remote)

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.

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.