Part-Time Clinical Research Coordinator: Consent & Data

Mount Sinai Morningside; New York (NY); On-site; USD 23,419 - 52,348; Part time

Job summary

Mount Sinai Morningside is seeking a part-time Clinical Research Coordinator to support daily study activities, obtain informed consent, and collect data for research protocols at our New York facility.

The role involves assisting in grant preparation, maintaining study files, coordinating with IRB submissions, and ensuring compliance and accurate documentation while supporting study participants and staff.

Qualifications

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

Research coordination

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 study activities, obtain informed consent, and collect data for research protocols at our New York facility.

The role involves assisting in grant preparation, maintaining study files, coordinating with IRB submissions, and ensuring compliance and accurate documentation while supporting study participants and staff.