Clinical Research Coordinator I - Data & Study Support

Mount Sinai; United States; On-site; USD 59,000 - 74,000; Full time

Job summary

Mount Sinai is seeking a Clinical Research Coordinator to support daily activities of clinical studies, including obtaining informed consent, collecting and organizing data, and maintaining study records in line with hospital procedures.

The role involves inputting information into databases, assisting with grant applications and IRB submissions, coordinating participant screening, and preparing for 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).
• Educates participants regarding study requirements.
• Assists in screening participants for eligibility and registering subjects with sponsoring agencies.
• Assists in preparing grant applications, IRB/GCO submissions, and filings.
• Maintains source documents and subject files; supports chart reviews.
• Secures, delivers and ships clinical specimens as required by the protocol.
• Prepares for monitoring visits and performs related duties.

Skills

Data entry

Informed consent administration

Study coordination

Education

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

Job description

Mount Sinai is seeking a Clinical Research Coordinator to support daily activities of clinical studies, including obtaining informed consent, collecting and organizing data, and maintaining study records in line with hospital procedures.

The role involves inputting information into databases, assisting with grant applications and IRB submissions, coordinating participant screening, and preparing for monitoring visits.