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.

Cape Fox Corporation, its subsidiaries, and affiliates provide equal employment opportunities to all persons and prohibit employment decisions on the basis of race, religion, color, creed, national origin, sex, age, disability, political affiliation, protected veteran status, or sexual orientation. Cape Fox Corporation, its subsidiaries, and affiliates offer preference to Cape Fox Corporation shareholders, descendants, and other Native Americans pursuant to Public Law 100-241.

Bachelor's degree - (Neuroscience, Psychology, Biology)

Required experience in analytical and statistical software program(s), e.g., SPSS, R, FSL, SPM, AFNI, MATLAB.