Part-Time Clinical Research Coordinator: Data & Consent

Mount Sinai Morningside; New York (NY); On-site; USD 23,000 - 52,000; Full time

Job summary

Mount Sinai Morningside is seeking a part-time Clinical Research Coordinator to support daily study activities, obtain informed consent, collect and organize data, and assist with grant-related documents under supervision. This hourly role qualifies for overtime as needed and emphasizes adherence to hospital procedures.

Responsibilities include data entry, subject screening, consent assistance, preparing IRB and sponsor submissions, and maintaining study notebooks and source documents to ensure

Qualifications

• Bachelor's degree in science or related field preferred or a combination of relevant research experience and education.

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.

Education

Bachelor's degree in science or related field preferred or equivalent

Job description

Mount Sinai Morningside is seeking a part-time Clinical Research Coordinator to support daily study activities, obtain informed consent, collect and organize data, and assist with grant-related documents under supervision. This hourly role qualifies for overtime as needed and emphasizes adherence to hospital procedures.

Responsibilities include data entry, subject screening, consent assistance, preparing IRB and sponsor submissions, and maintaining study notebooks and source documents to ensure