Clinical Research Coordinator I: Data, Consent & Study Support

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

Job summary

Mount Sinai Health System in New York is seeking a Clinical Research Coordinator to support daily study activities, obtain informed consent, and maintain study data. You will assist with grant documents and IRB submissions, ensure proper source documentation, and help with specimen management and monitoring visits.

The role offers exposure to diverse clinical studies and requires a science degree; no experience is required, though 1 year of research experience is preferred.

Qualifications

• Bachelor's or Masters 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 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 Masters degree in Science or closely related field

Job description

Mount Sinai Health System in New York is seeking a Clinical Research Coordinator to support daily study activities, obtain informed consent, and maintain study data. You will assist with grant documents and IRB submissions, ensure proper source documentation, and help with specimen management and monitoring visits.

The role offers exposure to diverse clinical studies and requires a science degree; no experience is required, though 1 year of research experience is preferred.