Clinical Research Program Coordinator

Mount Sinai Medical Center; New York (NY); On-site; USD 59,000 - 74,000; Full time

Job summary

Mount Sinai Health System in New York seeks a Research Program Coordinator to support the implementation and day-to-day coordination of a research study under the supervision of principal investigators. The coordinator will work closely with the research team to support participant recruitment, data collection, regulatory activities, and study database management.

The role involves coordinating IRB submissions, maintaining study documentation, and organizing regular team meetings, while ensuring

Qualifications

• Masters in Natural Sciences or Bachelors with 5 years of progressive research experience.
• 4 years of research experience in data management and study coordination.
• Preferred: experience with clinical research coordination, participant recruitment, or human subjects research.
• Strong organizational and interpersonal skills; ability to communicate with patients, investigators, and staff.
• Experience with electronic research databases and data entry; familiarity with IRB requirements.

Responsibilities

• Coordinate day-to-day research activities and support study implementation.
• Assist with patient recruitment, enrollment, and screening.
• Conduct follow-up assessments per protocol.
• Coordinate data collection, coding, and database management.
• Prepare regulatory documents and IRB submissions.
• Maintain study documentation and compliance.
• Organize weekly/biweekly research meetings.
• Support preparation of reports, manuscripts, and presentations.

Skills

Strong organizational skills

Interpersonal skills

Effective communication

Independent work with a multi-Discip团队

Education

Masters in Natural Sciences OR Bachelors plus 5 years of progressive research experience

Tools

Electronic research databases

Data entry

Job description

Mount Sinai Health System in New York seeks a Research Program Coordinator to support the implementation and day-to-day coordination of a research study under the supervision of principal investigators. The coordinator will work closely with the research team to support participant recruitment, data collection, regulatory activities, and study database management.

The role involves coordinating IRB submissions, maintaining study documentation, and organizing regular team meetings, while ensuring