Entry-Level Clinical Research Coordinator

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

Job summary

The Mount Sinai Health System in New York seeks a Clinical Research Coordinator to assist daily activities of clinical studies, obtain informed consent, collect and organize study information, and support grant documents such as IRB submissions.

You will collect and record data, educate participants, help with screening, subject registration, and prepare for monitoring visits, while maintaining source documents and ensuring data quality.

Qualifications

• Bachelor's 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 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 Masters degree in Science or closely related field

Job description

The Mount Sinai Health System in New York seeks a Clinical Research Coordinator to assist daily activities of clinical studies, obtain informed consent, collect and organize study information, and support grant documents such as IRB submissions.

You will collect and record data, educate participants, help with screening, subject registration, and prepare for monitoring visits, while maintaining source documents and ensuring data quality.