Senior Clinical Research Coordinator – Protocols & Data

Mount Sinai Medical Center; New York, Northern (NY, KY); Hybrid; USD 66,000 - 98,000; Full time

Job summary

Mount Sinai Health System coordinates the clinical assessments of study subjects under minimal supervision and analyzes moderately complex clinical research data. It prepares grant applications and documents and assists in protocol submissions (IRB, Grants and Contracts Office).

The role involves coordinating subject screening and evaluation, ensuring complete data through chart reviews, and supporting the PI and regulatory staff in new protocol submissions and amendments.

Qualifications

• Bachelor's degree in sciences or related field.
• 2 years of clinical research

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 reviews.
• Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials.
• Obtains informed consent under supervision of the Principal Investigator, Clinical Research Manager, or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects, and for studies involving genetic tests.
• Independently obtains informed consent for other clinical studies.
• Mentors Clinical Research Coordinators in training.
• Performs other related duties.

Education

Bachelors degree in sciences or related field

Job description

Mount Sinai Health System coordinates the clinical assessments of study subjects under minimal supervision and analyzes moderately complex clinical research data. It prepares grant applications and documents and assists in protocol submissions (IRB, Grants and Contracts Office).

The role involves coordinating subject screening and evaluation, ensuring complete data through chart reviews, and supporting the PI and regulatory staff in new protocol submissions and amendments.