Clinical Research Coordinator I: Data, Consent & Study Support

Mount Sinai Health System; United States; On-site; USD 52,000 - 78,000; Full time

Job summary

Mount Sinai Health System is seeking a Clinical Research Coordinator to support daily study activities, collect and organize data, and assist in consent processes. You will help prepare grant applications and IRB submissions, and maintain meticulous study records.

The role involves coordinating specimen handling, supporting monitoring visits, and ensuring compliance with hospital procedures. No prior experience is required, though research exposure is preferred.

Qualifications

• Collect and record study data.
• Obtain informed consent under supervision and educate participants.
• Assist with eligibility screening and enrollment activities.

Responsibilities

• Maintain source documents and subject files per hospital procedures.
• Secure, deliver and ship clinical specimens as required by protocol.
• Prepare for monitoring visits and assist in related duties.

Skills

Data collection

Study data entry

Informed consent administration

Education

Bachelors or Masters in Science or related field

Job description

Mount Sinai Health System is seeking a Clinical Research Coordinator to support daily study activities, collect and organize data, and assist in consent processes. You will help prepare grant applications and IRB submissions, and maintain meticulous study records.

The role involves coordinating specimen handling, supporting monitoring visits, and ensuring compliance with hospital procedures. No prior experience is required, though research exposure is preferred.