Part-Time Clinical Research Coordinator: Data & Consent

Mount Sinai Health System; New York (NY); On-site; USD 23,000 - 53,000; Part time

Job summary

The Mount Sinai Health System is seeking a Part-time Clinical Research Coordinator to support daily clinical research activities at a New York site. The role involves collecting and organizing study data, obtaining informed consent, and assisting in study-related tasks under supervision.

Responsibilities include data entry, participant screening, credentialing for sponsorship, and supporting grant applications and IRB submissions, with an emphasis on ensuring accurate documentation 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 and educates participants regarding study requirements.
• Assists in activities related to clinical research studies including answering calls, screening eligibility, registering subjects, and administering lifestyle questionnaires.
• Assists in preparing grant applications, IRB/GCO submissions and filings.
• Maintains source documents and subject files in accordance with hospital procedures and ensures complete subject data through chart reviews.
• Secures, delivers and ships clinical specimens as required by the protocol.
• Prepares for monitoring visits and performs other related duties.

Education

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

Job description

The Mount Sinai Health System is seeking a Part-time Clinical Research Coordinator to support daily clinical research activities at a New York site. The role involves collecting and organizing study data, obtaining informed consent, and assisting in study-related tasks under supervision.

Responsibilities include data entry, participant screening, credentialing for sponsorship, and supporting grant applications and IRB submissions, with an emphasis on ensuring accurate documentation and