Clinical Research Coordinator I: Entry-Level Research

Myana; New York (NY); On-site; USD 55,000 - 75,000; Full time

Job summary

Mount Sinai Health System in New York seeks a Clinical Research Coordinator to support daily study activities, obtain informed consent, and help organize study information. You will assist in data collection, recording entries in the database, and coordinating with investigators.

Responsibilities include preparing grant applications, IRB submissions, maintaining source documents, managing specimens, and assisting in monitoring visits.

Qualifications

• Bachelor's or Master's degree in Science or closely related field is required.
• 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.

Skills

Informed consent

Data collection

Study coordination

Education

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

Job description

Mount Sinai Health System in New York seeks a Clinical Research Coordinator to support daily study activities, obtain informed consent, and help organize study information. You will assist in data collection, recording entries in the database, and coordinating with investigators.

Responsibilities include preparing grant applications, IRB submissions, maintaining source documents, managing specimens, and assisting in monitoring visits.