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Ohio State University

Public research university in Columbus, OH

Clinical Research Coordinator - Pulmonary Critical Care and Sleep

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeColumbus, OH, USANo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in Biological Sciences, Health Sciences, Social Sciences, or another medical field, or an equivalent combination of education and experience, is required.
  • One year of relevant experience is required.
  • Candidates must successfully complete a background check; a pre-employment physical, including a drug screen, may be required.
  • Evening, weekend, holiday, and on-call availability is expected.
  • Proficient computer skills, including experience with Microsoft applications, are essential.

Responsibilities

  • Coordinate and perform daily clinical research activities in accordance with approved protocols for the Critical Care Trials Group.
  • Assess patient records to identify patients eligible for specified clinical research protocols.
  • Recruit, interview, and enroll patients; obtain informed consent and ensure the consent process complies with regulatory and sponsor requirements.
  • Educate patients and families about the purpose, goals, and processes of clinical studies.
  • Coordinate scheduling and follow-through of patient care appointments, procedures, and diagnostic testing in accordance with study protocols.
  • Participate in collecting, processing, and evaluating biological samples.
  • Administer, evaluate, and calculate standardized scoring for diagnostic, psychological, or behavioral testing or questionnaires.
  • Assist with monitoring patients for adverse reactions to study treatment, procedures, or medication; notify appropriate clinical professionals to evaluate patient response, identify complications, and provide an appropriate level of care.
  • Document unfavorable responses and notify research sponsors and applicable regulatory agencies.
  • Participate in evaluating patients for compliance with protocols.
  • Assist with collecting, extracting, coding, and analyzing clinical research data; generate reports and review them to ensure data validity.
  • Support compliance with Institutional Review Board, Food and Drug Administration, federal, state, and industry sponsor regulations.
  • Assist with coordinating and preparing for external quality assurance and control reviews by Institutional Review Boards, federal agencies, or industry sponsors.
  • Participate in developing new research protocols and contribute to establishing study goals to meet protocol requirements.

Desired Qualifications

  • Two to four years of relevant experience is preferred.
  • Experience or knowledge in the relevant specialty area is preferred.
  • Familiarity with medical terminology is desired.
  • Clinical research certification from an accredited agency is considered an asset.

About the Company

Ohio State University

Public research university in Columbus, OH

The Ohio State University is a comprehensive public research university that combines undergraduate, graduate, and professional education with research and public service.

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