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Research Associate II, Clinical Trials
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Full-time
- Collects project data through interviews, chart review or other methods.
- May assist in development of study tools (e.g. tracking forms, questionnaires, chart review forms, etc
- May interface with IRB and/ or draft portions of IRB protocols, amendments, continuing reviews, etc.
- Minimum two (2) years of experience in public health, healthcare administration, epidemiology, or healthcare-related field OR one (1) year of experience in public health, healthcare administration, epidemiology, or healthcare-related field AND Masters or terminal degree in public health, healthcare administration, epidemiology, or healthcare-related field
- Minimum one (1) year experience in handling, processing, and preparing biospecimens for laboratory analysis and/or transport OR Masters or terminal degree in public health, healthcare administration, epidemiology, or healthcare-related field.
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