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 seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and collect, maintain, and organize study information. The role includes assisting with grant applications and IRB submissions.

Responsibilities include data entry, participant education, eligibility screening, subject registration with sponsors, and lifestyle questionnaire administration, ensuring compliant documentation and timely monitoring visits.

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 degree in Science or closely related field

Job description

The Mount Sinai Health System seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and collect, maintain, and organize study information. The role includes assisting with grant applications and IRB submissions.

Responsibilities include data entry, participant education, eligibility screening, subject registration with sponsors, and lifestyle questionnaire administration, ensuring compliant documentation and timely monitoring visits.