Clinical Research Coordinator - Surgery

The
Department of Surgery is seeking an experienced Clinical Research Coordinator
to support interventional clinical trials across multiple divisions. This role
will be responsible for coordinating and managing study activities for both
drug and device trials, including participant recruitment, study implementation,
data collection, and ensuring compliance with all regulatory requirements, institutional
policies, and study protocols.

Hourly Salary Range: $36.37 - $58.52

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 judgment.
• 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. Al Required
• 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.