Clinical Research Assistant: Data & IRB Support

Mount Sinai Health System; New York (NY); On-site; USD 26,000 - 37,000; Full time

Job summary

Mount Sinai Health System seeks a Clinical Research Assistant to support daily activities of clinical studies, including collection and organization of study information and preparing grant documents for IRB and Grants & Contracts Office. This role provides clerical support to Clinical Research Coordinators in the assigned area.

Responsibilities include screening participants for eligibility, data entry, handling specimens, and assisting with monitoring visits, with a focus on accuracy and

Qualifications

• Associates Degree in Science or closely related field preferred or HS/GED plus two years of related experience.
• 1 year in research environment preferred.

Responsibilities

• Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires.
• Collects and records study data. Inputs all information into database.
• Assists in preparing grant applications, IRB/GCO for submission and filings.
• Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews.
• Secures, delivers and ships clinical specimens as required by the protocol.
• Assists in the preparation for monitoring visits.
• Performs other related duties.

Education

Associates Degree in Science or closely related field preferred or HS/GED plus two years of related experience

1 year in research environment preferred

Job description

Mount Sinai Health System seeks a Clinical Research Assistant to support daily activities of clinical studies, including collection and organization of study information and preparing grant documents for IRB and Grants & Contracts Office. This role provides clerical support to Clinical Research Coordinators in the assigned area.

Responsibilities include screening participants for eligibility, data entry, handling specimens, and assisting with monitoring visits, with a focus on accuracy and