Required:

• Bachelors Degree or 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.
  
• Analytical skills to assess clinical research protocols and regulatory requirements, define problems, formulate logical solutions, develop alternative solutions, make recommendations, and initiate corrective actions.
  
• Working knowledge of clinical research concepts, policies and procedures, and human safety protection regulations and laws.
  
• Knowledge of and experience working with a variety of local and external IRBs, scientific review and other research committees, national cooperative group sponsors, industry sponsors, federal and foundation funding organizations, etc.
  
• 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