**Job Description**

Under minimal supervision, coordinates the clinical assessments of the study subjects; analyzes and assists in interpreting moderately complex clinical research data. Prepares grant applications and documents and assists in protocol submissions (for e.g., Institutional Review Board, Grants and Contracts Office).

**Qualifications**

+ Bachelors degree in sciences or related field.
+ 2 years of clinical research

**Responsibilities**

1. Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.

2. Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.

3. Prepares and ensures grant applications, IRB/GCO documents are submitted.

4. Ensures accurate and complete compilation of subject data through chart reviews.

5. Assists the Principal Investigator and regulatory staff ...