Role OverviewThis is a part-time position, 16 hours/week, assisting with study design, protocol development, participant recruitment, data collection, and regulatory compliance in a clinical psychology research setting.
What You Will Do
Assists with study design and protocol development, recruits and screens research participants, conducts clinical interviews/assessment, manages research databases, and maintains regulatory documentation.
Why It Might Be a Fit
Must be enrolled in a clinical psychology doctoral program, with experiences in clinical research complementing pre-clinical didactic training.
Requirements
- Must be enrolled in high school, trade/vocational school or higher education institution
- Must be enrolled in a clinical psychology doctoral program
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