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Clinical Research Associate

  • Location: North
  • Salary: 30.00-37.00
  • Contract hours: ZeroHour

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About the job

Job description:Responsible for conducting Phase I-IV single
or multi center studies according to Federal Regulations and ICH
guidelines. Responsible for assisting senior staff in planning study
conduct, designing case report forms (CRFs), Contract Research
Organization (CRO) selection and management, selection and training of
investigator sites, planning and running study meetings, evaluation,
selection and training of new study investigators and writing and
assembling submissions. Responsible for writing basic study protocols,
monitoring or overseeing monitoring of investigational sites to ensure
protocol adherence, assuring timely enrollment of patients and retrieval
of CRFs from study sites, processing CRFs including data cleanup and
classification of data, and completion of study summary.

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