Clinical Research Coordinator I: Data, Consent & IRB

Mount Sinai Health System; New York (NY); On-site; USD 59,000 - 74,000; Full time

Job summary

Mount Sinai Health System is seeking a Clinical Research Coordinator in New York to assist in daily activities of clinical research studies, obtain informed consent, and maintain study data. The role includes preparing grant applications and IRB/GCO documents, as well as ensuring proper handling of subject files and clinical specimens.

Responsibilities also cover screening participants for eligibility, answering inquiries, and supporting monitoring visits.

Qualifications

• Bachelors or Masters 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 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 degree in Science or closely related field

Master's degree in Science or closely related field

Job description

Mount Sinai Health System is seeking a Clinical Research Coordinator in New York to assist in daily activities of clinical research studies, obtain informed consent, and maintain study data. The role includes preparing grant applications and IRB/GCO documents, as well as ensuring proper handling of subject files and clinical specimens.

Responsibilities also cover screening participants for eligibility, answering inquiries, and supporting monitoring visits.