Clinical Research Coordinator

UCLA HEALTH

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Description

The Clinical Research Coordinator contributes to the overall
operational management of clinical research/trial/study activities from design,
set up, conduct, through closeout. The position has responsibility for the
implementation of research activities for one or more studies. The incumbent
recognizes and performs necessary tasks to manage projects and prioritizes work
to meet necessary deadlines. The incumbent is responsible for planning and
organizing necessary tasks to ensure adherence to the study protocol and
applicable regulations, such as institutional policy and procedures, FDA Code
of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP).

The Clinical Research Coordinator collaborates with the Principal Investigator
(PI), ancillary departments, central research infrastructure teams, sponsors,
institutions, and other entities as needed to support the administration of all
aspects of studies, including, but not limited

to, compliant conduct, financial management, and adequate personnel support.

This is a 24 month, part-time limited position that may convert to career.

Salary Range: $33.63 – $54.11/HourlyQualifications

 All Required:

• Bachelors
  Degree or 1-3 years of previous study coordination or clinical research
  coordination experience. 
• Strong
  verbal and written communication skills along with strong interpersonal skills
  to effectively
  establish rapport, and build collaborate relationships.
• Strong
  organizational capabilities to organize multiple projects and competing
  deadlines for efficiency and cost effectiveness.
• Analytical
  skills sufficient to work and solve address problems and identify solutions
  with reasoned judgement.
• Ability
  to adapt to changing job demands and priorities; work flexible hours to
  accommodate research
  deadlines.
• Ability
  to respond to situations in an appropriate and professional manner.
• Ability
  to concentrate and focus in a work environment that contains distracting
  stimuli and competing deadlines. 
• Ability
  to be flexible in handling work delegated by more than one individual.
• Typing
  and computer skill/ability including word-processing, use of spreadsheets,
  email, data entry. Ability to navigate numerous software programs and applications. 
• Ability
  to handle confidential material information with judgement and discretion.
• Working
  knowledge of the clinical research regulatory framework and institutional
  requirements.
• Mathematical
  skills Sufficient to prepare clinical research budgets, knowledge of math
  ability and knowledge
  of clinical trials research budgeting process to assist with the preparation of
  clinical trial
  budgets.
• Working
  knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical
  Practice (GC)
  for clinical research.
• Be
  available to work in more than one environment, travel to meetings, off-site
  visits, conferences,
  etc.