To support multiple clinical and health services research projects, the part-time per diem Clinical Research Coordinator II will manage subject recruitment, administer study visits, and assist with data analysis while ensuring compliance with study protocols. Key responsibilities Recruits and evaluates study participants, conducts enrollment, and schedules study visits Administers qualitative interviews and quantitative assessments, maintaining accurate records of study activities Participates in data analysis, including qualitative coding and quantitative data cleaning, while coordinating study team meetings Required qualifications Master's degree or Bachelor's degree with 2-5 years of experience in a clinical research setting Experience with qualitative interviewing and coding strongly preferred Knowledge of REDCap is strongly preferred Strong interpersonal skills and cultural sensitivity are essential Proficiency in Microsoft Office Suite and ability to manage time effectively
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