Clinical Research Coordinator ,

Concentric Methods is seeking a Clinical Research Coordinator to join our team in Bethesda, MD, in support of the NIH.

Responsibilities:

• Supports clinical staff develop, implement, and maintain clinical research data files and materials.
• Perform data analysis of sensory, autonomic, and neuroimaging data.
• Collects research data and prepares information for inputs and analysis.
• Verify study participant information and collect data and results of testing.
• Perform accurate and timely data analysis, report results and findings and respond to sponsor queries.
• Set up, format, and enter data into spreadsheets to analyze information and create reports.
• Enter data into research databases, systems, and applications for ongoing studies.
• Conduct somatosensory and pain-related quantitative sensory testing.
• Supports the development of forms and questionnaires.
• Assist researchers develop, maintain, and complete study data collection forms and source documents.
• Assist staff writing and editing clinical research protocols and informed consent forms (ICFs) based upon templates.
• Review draft protocols, case report forms, and manuals of operations for clarity, and completeness.
• Work with staff on the design, development, and preparation of documents such as spreadsheets, letters, rosters, agendas, presentations, and meeting minutes/summaries.
• Assist researchers design patient Case Report Forms (CRFs).
• Work with investigators from multiple NIH institutes and center to design sensory, autonomic, and imaging testing procedures to best characterize pain conditions associated with individual conditions, treatments, and diseases.
• Supports the collection of data from patient charts, medical records, interviews, questionnaires, and diagnostic tests.
• Retrieve research-related information from medical records, hospital information system, and laboratory information system and create spreadsheets and other reports for use in study analysis.
• Conduct pain-related neuroimaging studies of patients and healthy volunteers.
• Monitors subject's progress and reports adverse events.
• Assist staff writing progress reports and contributions to peer-reviewed scientific manuscripts.
• Conduct autonomic testing of patients and healthy volunteers.
• Supports assembly, development, and review of new research projects.
• Assist researchers develop and maintain current and new research protocols.
• Participate in the writing of clinical protocols to study pain mechanisms.
• Supports the creation and management of clinical websites and web-based tools.
• Participate in the writing of scientific papers.

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