Clinical Research Coordinator I: Data, Consent & Grants

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 is seeking a Clinical Research Coordinator to support daily activities of clinical studies. You will obtain informed consent, collect and organize study data, and assist in preparing grant applications and IRB submissions.

Responsibilities include data entry, participant education, eligibility screening, specimen handling, and monitoring preparation. Requires a Bachelor’s or Master’s degree in science; no experience required, but one year of research

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 information into database.
• Obtains informed consent and educates participants on study requirements.
• Assists in screening participants for eligibility and registering subjects with sponsoring agency.
• Prepares grant applications, IRB/GC0 submissions and filings.
• Maintains source documents and subject files; ensures complete data compilation.
• Secures, delivers and ships clinical specimens per protocol.
• Prepares for monitoring visits; performs other related duties.

Education

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

Job description

The Mount Sinai Health System in New York, NY is seeking a Clinical Research Coordinator to support daily activities of clinical studies. You will obtain informed consent, collect and organize study data, and assist in preparing grant applications and IRB submissions.

Responsibilities include data entry, participant education, eligibility screening, specimen handling, and monitoring preparation. Requires a Bachelor’s or Master’s degree in science; no experience required, but one year of research