Location
New York
Job Type
Full-time
Posted
June 24, 2026
Job Description
**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
Non-Bargaining Unit, 843 - Obs/Gyn Reproductive Science - ISM, Icahn School of Medicine
**Responsibilities**
+ Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
+ Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
+ Prepares and ensures grant applications, IRB/GCO documents are submitted.
+ Ensures accurate and complete compilation of subject data through chart re...
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
Non-Bargaining Unit, 843 - Obs/Gyn Reproductive Science - ISM, Icahn School of Medicine
**Responsibilities**
+ Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
+ Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
+ Prepares and ensures grant applications, IRB/GCO documents are submitted.
+ Ensures accurate and complete compilation of subject data through chart re...
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