Clinical Research Coordinator, Santa Monica

The Clinical Research Coordinator contributes to the overall
operational management of clinical research/trial/study activities from design,
set up, conduct, through closeout. In this role, you will be responsible for
the implementation of research activities for one or more studies. Perform
necessary tasks to manage projects and prioritizes work to meet necessary
deadlines. You will be 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.

Hourly Salary Range: $33.63 - $54.11

Required:

• Bachelor's 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 judgment.
• Ability to adapt to changing job demands and priorities; work
  flexible hours to accommodate research deadlines.
• Ability to be flexible in handling work delegated by more than one
  individual.
• 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.