Clinical Research Coordinator I — Data & Consent

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

Job summary

Mount Sinai in New York, NY seeks a Clinical Research Coordinator to support daily activities of clinical research studies, obtain informed consent, and collect and organize study information. Responsibilities include data collection and entry, consent processes, participant screenings, grant preparation, IRB submissions, and maintenance of source documents and regulatory files.

Qualifications include a Bachelor's or Master's degree in science or closely related field; no experience is required,

Qualifications

• Requires a 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

Grant applications

Education

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

Job description

Mount Sinai in New York, NY seeks a Clinical Research Coordinator to support daily activities of clinical research studies, obtain informed consent, and collect and organize study information. Responsibilities include data collection and entry, consent processes, participant screenings, grant preparation, IRB submissions, and maintenance of source documents and regulatory files.

Qualifications include a Bachelor's or Master's degree in science or closely related field; no experience is required,