Regulatory Project Manager - Hematology/Oncology (Fully Remote)

We are seeking an experienced Regulatory Project Manager who will
be responsible for regulatory coordination of complex clinical research studies
within assigned units, departments or divisions. In this role, you will perform
detailed review 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.

Annual Salary Range: $78,500.00 - $163,600.00. Please note, the department's
target salary range is $78,500.00 - $121,000.00

Required:

• Minimum of 3+ years of
  experience of clinical research coordination
• 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.
• Demonstrated 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