Clinical Research Coordinator I: Start in Study Operations

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

Job summary

Mount Sinai Morningside is seeking a Clinical Research Coordinator I to support daily activities of clinical studies. The role involves obtaining informed consent, collecting and organizing study data, and assisting with grant applications and IRB/GCO submissions.

The coordinator will maintain study documents, ensure data accuracy, and manage sample logistics while supporting monitoring visits and other related duties as needed.

Qualifications

• Bachelor's or Master's degree in Science or closely related field.
• No experience required; one year of research experience preferred.
• Industry-sponsored clinical trials preferred.
• Regulatory 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 Master's degree in Science or closely related field

Job description

Mount Sinai Morningside is seeking a Clinical Research Coordinator I to support daily activities of clinical studies. The role involves obtaining informed consent, collecting and organizing study data, and assisting with grant applications and IRB/GCO submissions.

The coordinator will maintain study documents, ensure data accuracy, and manage sample logistics while supporting monitoring visits and other related duties as needed.