Part-Time Clinical Research Coordinator | Impactful Studies

Mount Sinai; New York (NY); On-site; USD 23,000 - 55,000; Part time

Job summary

Mount Sinai Health System in New York, NY, is seeking a Part-time Clinical Research Coordinator to support daily activities of clinical studies. The role involves obtaining informed consent, data collection, and maintaining study records while following hospital procedures.

The position is hourly and eligible for overtime for part-time employees. Responsibilities include assisting with grant applications, IRB filings, and coordinating with sponsors to ensure regulatory compliance and

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 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 data entry

Grant preparation

Education

Bachelor's degree in science or related field

Job description

Mount Sinai Health System in New York, NY, is seeking a Part-time Clinical Research Coordinator to support daily activities of clinical studies. The role involves obtaining informed consent, data collection, and maintaining study records while following hospital procedures.

The position is hourly and eligible for overtime for part-time employees. Responsibilities include assisting with grant applications, IRB filings, and coordinating with sponsors to ensure regulatory compliance and