Clinical Research Coordinator I: Data & Consent

Mount Sinai Morningside; New York (NY); On-site; USD 60,000 - 75,000; Full time

Job summary

Mount Sinai Health System is seeking a Clinical Research Coordinator to support the daily activities of clinical research studies, obtain informed consent, and manage study information. You will assist in preparing grant applications and documents (IRB, Grants and Contracts Office).

Responsibilities include collecting data, maintaining source documents, and handling specimens, with potential for minimal supervision and collaboration with investigators.

Qualifications

• Bachelor's or Master's degree in Science or closely related field.
• No experience required. One year of research experience preferred.

Responsibilities

• Collects and records study data. Inputs all information into database.
• Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
• 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.
• 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.
• Prepares for monitoring visits.
• Performs other related duties.

Education

Bachelor's or Master's degree in Science or closely related field

Job description

Mount Sinai Health System is seeking a Clinical Research Coordinator to support the daily activities of clinical research studies, obtain informed consent, and manage study information. You will assist in preparing grant applications and documents (IRB, Grants and Contracts Office).

Responsibilities include collecting data, maintaining source documents, and handling specimens, with potential for minimal supervision and collaboration with investigators.