Clinical Research Supervisor 1 - Hematology/Oncology

The
Clinical Research Supervisor oversees routine research coordination and unit
operations to ensure compliance with policies, procedures, and internal
controls. Manages clinical studies from start-up through closeout in accordance
with protocols and regulatory requirements, including FDA CFR and ICH GCP.
Serves as a liaison with the PI, internal teams, and sponsors to support compliant
study conduct, financial oversight, and staffing needs.

Annual Salary Range: $86,400.00 - $184,800.00

Required:

• Bachelor's degree required, Master's degree
  preferred
• Minimum of 5+ years of experience in a
  clinical research setting
• 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 effectively communicate to and
  interact with patients in a compassionate and kind manner.
• 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. Ability to adapt to changing
  job demands and priorities, remain flexible including working flexible hours to
  accommodate research deadlines.
• 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.
• 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.
• Strong verbal and written communication skills
  to effectively establish rapport, building collaborative relationships, and
  communicate complex concepts and ideas in an easy-to-understand manner.
• Ability to handle confidential information
  with judgement and discretion.
• Availability to work in more than one
  environment, travelling to various clinic sites, meetings, conferences, etc.
• Advanced 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.
• Demonstrated ability to interpret IRB, FDA,
  federal and UCLA requirements and utilize that information to guide
  investigators and other team members.
• Expert level working knowledge of clinical
  research concepts, policies and procedures, and human safety protection
  regulations and laws.
• Demonstrated experience and knowledge of
  clinical trials budgeting processes to manage the preparation of clinical trials
  budgets.
• Demonstrated experience with FDA processes and
  procedures.
• Ability to lead the development and
  implementation of quality improvement activities, SOPs, processes, etc.
• Team leadership experience (i.e. projects,
  committees, etc.).
• Ability to develop and give presentations to
  leadership, positively representing the department.
• Ability to predict potential problems and
  proactively implement solutions.
• Ability to clearly communicate complex
  departmental and institution-wide policies and ensure understanding.
• Ability to manage complex and sometimes
  conflicting departmental priorities and external timelines.

Preferred:

• Clinical Research Certification (CCRP, ACRP,
  etc.)