Clinical Trials Assistant
The Clinical Trials Assistant (CTA) supports the clinical team in the start-up, maintenance, and closeout of clinical studies. Primary responsibilities include: order, prepare, distribute study and specimen supplies, and maintain tracking information; collect, maintain, and review essential documents in the Trial Master File; maintain study data and metrics in clinical trial management systems and trackers; coordinate and track specimen shipments from clinical sites; and track and manage Case Report Forms (CRFs), queries and clinical data flow.
- Associate’s degree or equivalent and minimum three (3) years of related experience in the clinical research, clinical care or related field, OR a Bachelor’s Degree in a science-related field.
- Basic knowledge and understanding of CFR and GCP/ICH guidelines.
- Bachelor’s Degree.
- Medical terminology background or the ability to learn medical terminology.
- Basic understanding of clinical research processes.
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