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.

**Required Education and Experience**
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.

**Required Credentials**
N/A.

**Preferred**
Bachelor’s Degree.
Medical terminology background or the ability to ...