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Clinical Research CoordinatorThe Ohio State University Wexner Medical CenterColumbus, Ohio, United States

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Clinical Research Coordinator

The Ohio State University Wexner Medical Center
  • US
    Columbus, Ohio, United States
  • US
    Columbus, Ohio, United States

À propos

Position Summary

The Clinical Research Coordinator will perform daily clinical research activities in accordance with approved protocols administered by Dr. Sullivan within the School of Health and Rehabilitation Sciences.

Responsibilities

  • Assist with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols
  • Recruits, interviews and enrolls patients; obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements
  • Educates patients and families of purpose, goals, and processes of clinical study
  • Coordinates scheduling and follow-through of patient care appointments, procedures, & other diagnostic testing in accordance with study protocol
  • Administers, evaluates and calculates standardized scoring of psychological or behavioral testing or questionnaires
  • Assists with monitoringpatients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications, & provide appropriate level of care
  • Documents unfavorable responses and notifies research sponsors & applicable regulatory agencies
  • Participates in evaluating patients for compliance related to protocol
  • Assists with collecting, extracting, coding, and analyzing clinical research data
  • Generates reports and reviews to ensure validity of data
  • Supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations
  • Assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors
  • Participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements

Job Requirements

Bachelor's Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education experience required. 1 year of relevant experience required. 2-4 years of relevant experience preferred.

Research and Scholarship - Clinical Research - Individual Contributor - S2

Regular 40 First Shift

  • Columbus, Ohio, United States

Compétences linguistiques

  • English
Avis aux utilisateurs

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