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, NY is seeking a Clinical Research Coordinator to support daily activities of clinical studies. You will obtain informed consent, collect and organize study data, and assist with grant applications and IRB/GCO submissions.

Responsibilities include data entry, participant screening, specimen handling, and preparation for monitoring visits, with potential familiarity with institutional processes and regulatory requirements.

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.

Skills

Informed consent

Data collection

Study coordination

Education

Bachelor's or Master's in Science

Job description

The Mount Sinai Health System in New York, NY is seeking a Clinical Research Coordinator to support daily activities of clinical studies. You will obtain informed consent, collect and organize study data, and assist with grant applications and IRB/GCO submissions.

Responsibilities include data entry, participant screening, specimen handling, and preparation for monitoring visits, with potential familiarity with institutional processes and regulatory requirements.