Impactful Clinical Research Coordinator

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

Job summary

Mount Sinai Morningside seeks a Clinical Research Coordinator to support daily activities of clinical research studies, including obtaining informed consent and collecting and organizing study data. You will assist in grant applications and IRB/GCO submissions, while maintaining source documents and subject files according to hospital procedures.

The role involves securing and shipping specimens as required, preparing for monitoring visits, and performing related duties to ensure compliance and

Qualifications

• Requires a bachelor's or master's degree in science or closely related field.
• No prior 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 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

Bachelors or Masters degree in Science or closely related field

Job description

Mount Sinai Morningside seeks a Clinical Research Coordinator to support daily activities of clinical research studies, including obtaining informed consent and collecting and organizing study data. You will assist in grant applications and IRB/GCO submissions, while maintaining source documents and subject files according to hospital procedures.

The role involves securing and shipping specimens as required, preparing for monitoring visits, and performing related duties to ensure compliance and