Clinical Research Coordinator I — Data, Consent & Studies

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 seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and manage study data. You will help prepare grant applications and ensure proper documentation for IRB and contract offices.

Responsibilities include data collection, participant education, eligibility screening, and handling specimens, with opportunities to contribute to monitoring visits and regulatory filings.

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 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.

Skills

Informed consent

Data collection

Study coordination

Data entry

Communication

Education

Bachelor's or Master's degree in Science or related field

Job description

The Mount Sinai Health System in New York, NY seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and manage study data. You will help prepare grant applications and ensure proper documentation for IRB and contract offices.

Responsibilities include data collection, participant education, eligibility screening, and handling specimens, with opportunities to contribute to monitoring visits and regulatory filings.