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Clinical Research Coordinator II - Orthopedic Surgery

External
Washington University in St. Louis logoWashington University In St. Louis · Washington University Medical Campus
Full-timeHybridToday
ClassificationComplianceSASStatistical Analysis
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Requirements

  • Not Applicable
  • Driver's License:
  • A driver's license is not required for this position.
  • More About This Job
  • Required Qualifications
  • Basic Life Support certification (Online Basic Life Support certifications, those without a skills assessment component, are not sufficient to meet the Basic Life Support requirements). Basic Life Support certification must be obtained within one month of hire date.
  • Education:
  • No additional education unless stated elsewhere in the job posting.
  • Certifications /Professional Licenses :
  • No additional certification/professional licenses unless stated elsewhere in the job posting.
  • Work Experience:
  • No additional work experience unless stated elsewhere in the job posting.
  • Clinical Research, Clinical Study Protocols, Database Management, Research Projects, Spreadsheet Analysis, Statistical Analysis Software (SAS)
  • Grade
  • C10
  • Salary Range
  • $52,600.00 - $78,900.00 / Annually
  • Questions
  • For frequently asked questions about the application process, please refer to our External Applicant FAQ .
  • Accommodation
  • If you are un

Benefits

Vision insuranceEquity / stock options

Additional Information

Scheduled Hours 40 Position Summary The Clinical Research Coordinator II (CRC II) will manage all phases of clinical research studies within the division, focusing on improving outcomes for pediatric orthopaedic surgery patients. This hybrid role requires an on-campus presence for team collaboration and to actively enroll patients ranging from infants to 17 years old, requiring exceptional interpersonal skills to engage warmly with both children and their parents. Beyond core coordination, this position manages study regulations and requires a strong understanding of WashU policies and IRB regulations. Responsibilities include preparing new study submissions and providing dedicated IRB/regulatory support to fellows, residents, medical students, and research scholars. As a key departmental representative, the coordinator must possess strong customer service skills to effectively interface with our faculty and their nationwide peer collaborators. Job Description Primary Duties & Responsibilities: Assists in developing plans for research projects and discusses the interpretation of results; collaborates in the preparation of manuscripts for publications and preparation of grant proposals to sponsoring agencies; assists in the preparation of amendments to protocols and/or modifications to study design as appropriate. Coordinates the development of forms, questionnaires and the application of research techniques; assists in writing instructional procedure manuals for study progress, data collection and coding; reviews journals, abstracts and scientific literature to keep abreast of new developments and to obtain information regarding previous studies to aid in the planning of new studies. Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants' progress in the study; analyzes, investigates and reports adverse events; makes decisions as when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency. Evaluates and interprets collected clinical data as appropriate; prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions of the same. Performs other duties as assigned. Working Conditions: Job Location/Working Conditions Patient care setting. Physical Effort Typically sitting at desk or table. Equipment Office equipment. The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel so classified. Management reserves the right to revise or amend duties at any time. Required Qualifications Education: Bachelor's degree or combination of education and/or experience may substitute for minimum education. Certifications /Professional Licenses : The list below may include all acceptable certifications, professional licenses and issuers. More than one credential, certification or professional license may be required depending on the role. Basic Life Support - American Heart Association, Basic Life Support - American Red Cross Work Experience: Clinical Research (2 Years)


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Clinical Research Coordinator II - Orthopedic Surgery at Washington University In St. Louis