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Clinical Research Coordinator

Company: Equiliem
Location: Bethesda
Posted on: November 17, 2022

Job Description:

Job DescriptionThis position will independently provide support services to satisfy the overall operational objectives of the NCI/CCR. Minimum Education Bachelor''s Resume Max Pages 3 Certifications & Licenses * Min 1 year of related research exp, incl exp in cancer patient outcomes research * Exp should incl use of questionnaires, interviews, neuropsych testing & obtaining biologic samples * Bachelor''s degree Skills (Ranked By Priority) 1. Excellent analytical, organizational and time management skills. 2. Strong verbal and written communication skills. 3. Past experience in data coding and entry and analysis of data using Excel, SPSS, or Stata required 4. Past experience using reference management software 5. Past experience in writing research data reports 1, 2, 3, 4, 5 _represents priority rankings, where 1 is highest priority and 5 is lowest priority of those ranked_ Software * MS Office Suite * SPSS or Stata required * POTS * dobe Acrobat * Stata Field of Study * Multi-Disciplinary or General Science * General Medical and Health Services DELIVERABLES * Work products and documents related to providing coordination of various clinical research projects, including both behavioral and clinical management trials. - Ad-Hoc * Work products and documents related to oversee daily operation of projects, recording, and evaluating data obtained in accordance with methods requested; overseeing technicians or students in their work and assist them as assigned or delegated. - Ad-Hoc * Work products and documents related to tracking data for clinical studies, preparation for audits and continuing reviews and coordinating this effort with institutional regulatory offices such as the IRB as well asClinical Research Management. - Ad-Hoc * Work products and documents related to oversee daily operation of projects, recording, and evaluating data obtained in accordance with methods requested; overseeing techni-cians or students in their work and assist them as assigned or delegated. - Ad-Hoc STATEMENT OF WORK DETAILS functional responsibility Supports clinical staff develop, implement and maintain clinical research data files and materials. description * Provide coordination of all Outcomes Section clinical research projects, including both behavioral and clinical management trials 1 description * Monitor technicians or students in their work and assist them as assigned 5 description * Develops scope of work and lead orientation of trainees and other staff description * Provide evaluation metrics of Outcomes Section staff and participates in annual reviews functional responsibility Collects research data and prepares information for inputs and analysis. description * Collaborate or assist with supervisor and senior research staff in preparation of scientific reports and manuscripts 3 description * Monitor and prepare reports for study audits, continuing reviews description * Coordinate study interim analysis and amendments in collaboration with institutional regulatory offices functional responsibility Supports the development of forms and questionnaires. description * N/A functional responsibility Supports the collection of data from patient charts, medical records, interviews, questionnaires, and diagnostic tests. description * Monitor daily operation of projects, recording, and evaluating data obtained in accordance with methods requested, including but not limited to data collection and entry, data collection and storage quality maintenance 2 functional responsibility Monitors subject''s progress and reports adverse events. description * N/A functional responsibility Supports assembly, development and review of new research projects. description * N/A functional responsibility Supports the creation and management of clinical websites and web-based tools. description * N/A functional responsibility Organizes and performs clinical research, utilizing internet and other available clinical resources. description * Track data for clinical studies and coordinating this effort with institutional regulatory offices such as the IRB as well as Clinical Research Management 4 1, 2, 3, 4, 5 _represents priority rankings, where 1 is highest priority and 5 is lowest priority of those ranked_

Keywords: Equiliem, Bethesda , Clinical Research Coordinator, Other , Bethesda, Maryland

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