Clinical Research Coordinator III

Rutgers University

New Brunswick, NJFull-time

Behavioral Health Market Context

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Qualifications

  • •Bachelor's degree in relevant Life Science is required
  • •Equivalent education, experience, and/or training may be substituted for the degree requirement
  • •Experience working in a fast-paced environment
  • •Lifting to 25lbs
  • •Work Environment: Open office and medical / laboratory environments
  • •2 more items(s)

Responsibilities

  • •The Clinical Research Coordinator III will play an important role within the Neurosurgery research team by providing assistance to the Clinical Research Manager in the day-to-day tasks required within the Clinical Research Unit of RWJMS Department of Neurosurgery
  • •The Clinical Research Coordinator supports the Department's clinical research studies; assists with implementation and coordination of studies; participates in recruitment of study participants; performs behavioral or diagnostic testing; assists with collection, maintenance and reporting of clinical research data
  • •Assist with development and implementation of plans to recruit and retain study participants; assist with interviewing, recruitment and enrollment of human subjects for participation in clinical protocol; distribute and explain processes and goals of clinical studies to participants; assist with development of clinical study informational and educational materials; assist with informed consent process
  • •May conduct screening, baseline and annual assessments according to standardized procedures; obtain medical histories from participants; review and abstract data from medical records; assist with patient evaluations
  • •Participate in development of study questionnaires; may assist with behavioral or diagnostic testing, or administration of questionnaires; assist with scoring of standardized questionnaires and development of behavioral coding systems
  • •May perform basic laboratory procedures to collect and process biological specimens; collect, log, and track samples and vital signs; documents study procedures
  • •Assist with collecting, entering and maintaining clinical research data into study database; prepare documentation and data for research progress reports to study sponsors; assist with completion of Institutional Review Board (IRB), Clinical Research Center (CRC), and/or sponsor study documents
  • •Physical Demands: Standing, sitting, walking, talking and hearing
  • •5 more items(s)
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