Assistant Clinical Research Coordinator - Hematology/Oncology

The
Assistant Clinical Research Coordinator assists the Clinical Research Coordinator
and/orSenior Clinical Research Coordinator in
contributing to the overall operational management ofclinical research/trial/study activities. In
this role, you will perform necessary tasks to assist inmanaging projects and prioritizing work to
meet necessary deadlines. You will provide support in planning and organizing
necessary tasks to ensure adherence to the study protocol and applicable regulations.

Hourly Salary Range: $29.28 - $47.10

Required:

• Minimum of 1+ years of
  experience in a clinical research setting
• 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.
• 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.
• Ability to handle
  confidential information with judgement and discretion.
• 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.

Preferred:

• Bachelor's Degree in related
  area and/or equivalent combination of education and experience