Part-Time Clinical Research Coordinator: Data & Consent

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

Job summary

Mount Sinai Morningside is seeking a part-time Clinical Research Coordinator to support daily clinical research activities in New York. The role involves obtaining informed consent, collecting data, and assisting with study logistics and grant-related filings.

The position is hourly and eligible for overtime for part-time staff, with duties including data management, consent education, and coordination of study materials and regulatory documents.

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

Education

Bachelor's degree in science or related field

Job description

Mount Sinai Morningside is seeking a part-time Clinical Research Coordinator to support daily clinical research activities in New York. The role involves obtaining informed consent, collecting data, and assisting with study logistics and grant-related filings.

The position is hourly and eligible for overtime for part-time staff, with duties including data management, consent education, and coordination of study materials and regulatory documents.