четверг, 26 сентября 2013 г.

Clinical Research Coordinator at Spokane

Job Description

Clinical Research Coordinator dutes and Responsiblities:

 

  • Plans and coordinates the initiation of research study protocol, and the establishment of operating policies and procedures.
  • Plans, implements, and maintains data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data.
  • Recruits, instructs, and coordinates research subjects and/or volunteers, as appropriate to specific study objectives and work scope.
  • Ensures the smooth and efficient day-to-day operation (as needed) of research and data collection activities; acts as the primary administrative point of contact for internal research staff and as the principle operational liaison for other research organizations, funding agencies and regulating bodies.
  • Coordinates the day-to-day activities (as needed) of any technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position; may perform aspects of research protocol, as required, in accordance with specified program objectives.
  • Monitors the progress of research activities; develops and maintains records of research activities, and prepares periodic and ad hoc reports, as required by investigators, administrators, funding agencies, and/or regulatory bodies.
  • To implement quality control process throughout the conduct of the trial
  • Job Requirements

    Clinical Research Coordinator Requirements:

    EDUCATIONAL REQUIREMENTS:

     

  • Minimum of a two-year degree in nursing or a four-year degree in a health care/science related field
  • SPECIALIZED CERTIFICATES/LICENSES:

  • At least 2 years of experience that is directly related to the duties and responsibilities specified
  • TRAINING/EXPERIENCE CLINICAL REQUIREMENTS:

  • Minimum of two years clinical research experience
  • GCP training
  • IATA certification (dangerous goods regulations as they pertain to biological specimens)
  • Diabetic neuropathy or nephrology experience a plus
  • TRANSFERABLE COMPETENCY REQUIREMENTS:

  • Verbal communications skills
  • Problem-solving skills
  • Planning/organizational skills
  • Personal motivation
  • Project management capabilities
  • Customer service skills
  • SPECIFIC TECHNICAL COMPETENCY REQUIREMENTS

  • Understanding of ICH/GCP guidelines for human research
  • Understanding of Code of Federal Regulations for Human Subjects
  • Computer Competency including proficiency in Microsoft Word and Excel
  • Understanding Phases I-IV drug development processes
  • ECG, phlebotomy skills, and any other technical skills related to the completion of a study visit as required by the protocol.
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    PHYSICAL REQUIREMENTS AND/OR ENVIRONMENTAL FACTORS

  • Work is normally performed in a typical interior/office work environment
  • Exposure to human bodily fluids
  • Laboratory processing and shipping procedures
  • Subject/Patient Care
  • Extensive Computer Use
  • Occasional on-call night and weekend work schedules
  • Lifting up to 20 pounds and occasionally more than 20 pounds
  • Ability to receive notice and communicate via cell phone
  • Ability to drive and daily availability of an automobile

  • Country: USA, State: Washington, City: Spokane, Company: InVentiv Health.

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