Clinical Research Associate I
Schedule study home visits and manage study calendar. Conduct home visits including physical measurements of child and parent, psychometric testing, actigraphy set up, and explanation of surveys and diaries to parents. Record and enter assessment results, draft report of findings, and communicate with family's case manager. Establish and maintain rapport with families to optimize the accuracy of assessment and retention of families in a longitudinal study.
Assist the assigned division research team in the organization, implementation and completion of clinical research trials. Maintain regulatory documents; assist the Principal Investigator in the planning of protocol implementation and site initiation visits and routine monitoring of clinical studies. Along with the PI, ensure that research projects are conducted in compliance with federal regulations, institutional/departmental guidelines, and standards of Good Clinical Practice.
Required Education/Experience: - Bachelor's Degree in Social Studies, Biology, or related scientific discipline, or equivalent combination of education and experience. - Minimum of one (1) year of related research experience. - Confirmed proficiency in a second language via successful completion of a language assessment may be required for certain departments. Required Credentials: - N/A Preferred: - Pediatric research experience.
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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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