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 collaborative relationships.
  
• 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 concentrate and focus in a work environment that contains distracting stimuli and competing deadlines.
  
• 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.