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Wash U

Academic research and entrepreneurial institution

Clinical Research Coordinator 2 - Medical Oncology

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeSt. Louis, MO, USA$54.6k - $81.9k /yr

About the Job

Requirements

  • A bachelor's degree is required, although a combination of education and/or experience may substitute for the minimum education requirement.
  • Two years of clinical research experience are required.

Responsibilities

  • Assist investigators as a data coordinator for clinical research trials of varying complexity, extracting data from the electronic medical record and other source documents and entering it into an electronic data capture system.
  • Help ensure accurate collection of study-required procedures while patients receive protocol treatment and participate in active protocol follow-up.
  • Act as a liaison among the school, trial sponsors, vendors, and study team.
  • Help the clinic coordinator and principal investigator manage and record data for all phases of study protocols as required by the institutional review board or sponsoring agency, ensuring compliance, patient safety and welfare, and data integrity.
  • Assist in developing research project plans and discussing interpretation of results; collaborate on manuscripts for publication, grant proposals to sponsoring agencies, and protocol amendments or study-design modifications.
  • Coordinate the development of forms and questionnaires and the application of research techniques; assist in writing instructional procedure manuals for study progress, data collection, and coding.
  • Review journals, abstracts, and scientific literature to keep current on developments and identify information about previous studies to aid planning new studies.
  • Implement and manage all phases of study protocols; ensure compliance with protocol guidelines and regulatory agency requirements; establish record-keeping systems; assess participants' study progress; analyze, investigate, and report adverse events; determine when to notify physicians, stop participant inclusion, or make or recommend protocol adjustments for participants; resolve protocol management issues and recommend corrective action; and serve as liaison with funding or sponsoring agencies.
  • Evaluate and interpret collected clinical data as appropriate; prepare oral or written presentations, reports, and analyses describing progress trends and providing recommendations or conclusions.
  • Perform other duties as assigned.

Desired Qualifications

  • SOCRA or ACRP certification is optionally listed, depending on the department.
  • Preferred skills include clinical research, clinical study protocols, database management, research projects, spreadsheet analysis, and statistical analysis software (SAS).

About the Company

Wash U

Academic research and entrepreneurial institution

Wash U turns groundbreaking research from Washington University in St. Louis into practical knowledge, technologies, and programs that benefit society by funding research, translating discoveries, and forming partnerships for technology transfer and entrepreneurship. It moves ideas from the lab to real-world use through translation, licensing, and collaboration with industry and other researchers. The university stands out due to its combination of high-impact research, Nobel-level expertise, transparent financial reporting, and a proven path for turning discoveries into public benefits through partnerships and entrepreneurship. Its goal is to build collaborative ecosystems that address global challenges and help create a more equitable future.

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Founded
1853

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