Senior Health Research Coordinator

Weill Cornell Medicine; New York (NY); On-site; USD 70,000 - 100,000; Full time

Job summary

Weill Cornell Medicine in New York, NY seeks a Senior Research Coordinator to support multi-center health services research projects. You will mentor staff, liaise with investigators and funders, and organize study data throughout the research process.

The role involves coordinating regulatory activities, preparing reports, and assisting in grant submissions, with a focus on good clinical practices and data integrity.

Qualifications

• Supports implementation, coordination, and monitoring of multi-center health services research studies.
• Mentors junior staff; liaises with investigators, funders, and collaborators.
• Manages regulatory files and ensures compliance with IRB and other agencies.
• Prepares data, reports, and meeting summaries; assists in study form/SOP design.
• Oversees study data collection, data entry, cleaning, and database creation.
• Communicates study details to participants and assists with informed consent.

Responsibilities

• Assists with maintaining regulatory files and ensuring compliance.
• Attends meetings with investigators and senior staff; coordinates data and reports.
• Provides input on study forms, SOPs, recruitment, data collection, and databases.
• Trains staff in implementing statistical analysis codes; mentors junior staff.
• Leads coordination of multi-site research projects and dissemination of materials.
• Ensures adherence to protocol guidelines and regulatory requirements.

Skills

IRB submissions

Regulatory compliance

Study coordination

Mentoring

Data management

English proficiency

Education

Bachelor's Degree

Master's degree preferred

Job description

Weill Cornell Medicine in New York, NY seeks a Senior Research Coordinator to support multi-center health services research projects. You will mentor staff, liaise with investigators and funders, and organize study data throughout the research process.

The role involves coordinating regulatory activities, preparing reports, and assisting in grant submissions, with a focus on good clinical practices and data integrity.