Clinical Research Coordinator - Hematology/Oncology (Limited)

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.

Hourly Salary Range:
$35.31 - $56.82

This is a limited
position that may convert to career.

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.