Clinical Research Assistant
Conduct follow-up study assessment home visits, which include physical measurements of child and parent, psychometric testing, actigraphy set up, and explanation of surveys and diaries to parents. Record and enter data, including assessment results. Establish and maintain rapport with families to optimize the accuracy of assessment and retention of families in a longitudinal study.
Assist and provide administrative support for assigned Division research team with specific aspects of the organization, implementation and completion of clinical research trials. Coordinate the recruitment, enrollment and scheduling of study participants. Track regulatory documents and correspondence, maintain study files, collect and enter data and maintain databases, and assist the PI or Clinical Study Manager in the general implementation of clinical studies.
Required: - High School Diploma or equivalent - Two (2) years of college-level coursework in biological or life sciences or health related field - At least one (1) year of work experience Preferred: - Bachelors Degree in biological or life sciences or health related field - At least three (3) years in a research or health care setting - Familiarity with US Food & Drug Administration (FDA) regulations and International Conference on - Harmonization (ICH) and Good Clinical Practice (GCP) guidelines - Knowledge of medical terminology
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Clinical Research Associate
Shannon works with sites across the nation that conduct cystic fibrosis trials to ensure that they have everything they need to perform their life-saving clinical research successfully.
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