Clinical Research Coordinator - Hematology/Oncology (Santa Monica)

The Clinical
Research Coordinator contributes to the overall operational management of
clinicalresearch/trial/study
activities from design, set up, conduct, through closeout. In this role, you
will beresponsible for
the implementation of research activities for one or more studies. Perform
necessarytasks to manage
projects and prioritizes work to meet necessary deadlines. You will be
responsible forplanning and
organizing necessary tasks to ensure adherence to the study protocol and
applicableregulations, such
as institutional policy and procedures, FDA Code of Federal Regulations (CFR),
andICH Good Clinical
Practice (GCP). The Clinical Research Coordinator collaborates with the
PrincipalInvestigator
(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 notlimited to,
compliant conduct, financial management, and adequate personnel support.

Hourly Salary
Range: $36.37 - $58.52

Required:

• Bachelor's
  degree in related area and/or equivalent combination of education and
  experience.
• Minimally
  2+ years of previous study coordination or clinical research coordination
  experience
• 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.
• 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.
• 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 adapt to changing job demands and priorities, remain flexible including
  working flexible hours to accommodate research deadlines.
• High
  degree of concentration and focus in a work environment that contains
  distracting stimuli, competing deadlines, and work delegated by more than one
  individual
• Availability
  to work in more than one environment, travelling to various clinic sites,
  meetings, conferences, etc.