Entry-Level Clinical Research Coordinator

Mount Sinai; United States; On-site; USD 55,000 - 75,000; Full time

Job summary

Mount Sinai is seeking a Clinical Research Coordinator I to support daily activities of clinical studies, obtain informed consent, and organize study information. The role includes data entry, participant education, and data quality assurance.

The candidate will assist in preparing grant applications and IRB/GCO submissions, maintain source documents, and coordinate specimen shipping and monitoring visits as required.

Qualifications

• No experience required; one year of research experience preferred.
• Industry-sponsored clinical trials experience preferred.
• Regulatory experience preferred.

Responsibilities

• Collects and records study data and inputs all information into database.
• Obtains informed consent under minimal supervision and educates participants on study requirements.
• Screens participants for eligibility and registers subjects with sponsoring agency.
• Maintains source documents and subject files per hospital procedures; ensures complete subject data through chart reviews.
• Assists in preparing grant applications and documents (IRB, Grants and Contracts Office).
• Prepares for monitoring visits and ships clinical specimens as required by protocol.
• Performs other related duties.

Skills

Data collection

Informed consent

Participant communication

Education

Bachelors or Masters degree in Science or closely related field

Job description

Mount Sinai is seeking a Clinical Research Coordinator I to support daily activities of clinical studies, obtain informed consent, and organize study information. The role includes data entry, participant education, and data quality assurance.

The candidate will assist in preparing grant applications and IRB/GCO submissions, maintain source documents, and coordinate specimen shipping and monitoring visits as required.