Clinical Research Coordinator I: Data & Study Support

Myana; New York (NY); On-site; USD 55,000 - 75,000; Full time

Job summary

The Mount Sinai Health System in New York seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and manage study data. Responsibilities include data collection, maintaining source documents, assisting with grant applications and IRB filings, coordinating with sponsors, and preparing for monitoring visits.

A Bachelor’s or Master’s degree in Science or related field is required; no experience is needed, with preferred 1 year of research

Qualifications

• Bachelor's or Master's degree in Science or related field.
• No experience required; one year of research experience preferred.

Responsibilities

• Collects and records study data and inputs into database.
• Obtains informed consent under supervision and educates participants on study requirements.
• Assists with grant applications and IRB/GCO submissions and filings.
• Maintains source documents and subject files per hospital procedures; ensures complete data through chart reviews.
• Secures, delivers and ships clinical specimens as required by the protocol.
• Prepares for monitoring visits and assists with related duties.

Skills

Informed consent procedures

Data entry

Study coordination

Education

Bachelor's or Master's degree in Science or related field

Job description

The Mount Sinai Health System in New York seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and manage study data. Responsibilities include data collection, maintaining source documents, assisting with grant applications and IRB filings, coordinating with sponsors, and preparing for monitoring visits.

A Bachelor’s or Master’s degree in Science or related field is required; no experience is needed, with preferred 1 year of research