Entry-Level Clinical Research Coordinator

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

Job summary

Mount Sinai's Institute for Critical Care Medicine (ICCM) in New York seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and organize study data. You will assist in grant preparation and IRB filings, and help ensure regulatory compliance.

Responsibilities include data collection and entry, screening participants, coordinating with sponsors, preparing for monitoring visits, and maintaining source documents and subject files according to

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) 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's Institute for Critical Care Medicine (ICCM) in New York seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and organize study data. You will assist in grant preparation and IRB filings, and help ensure regulatory compliance.

Responsibilities include data collection and entry, screening participants, coordinating with sponsors, preparing for monitoring visits, and maintaining source documents and subject files according to