Senior Research Coordinator

Weill Cornell Medicine; New York (NY); Sur place; USD 82 000 - 90 000; Plein temps

Résumé du poste

Weill Cornell Medicine in New York City is seeking a Senior Research Coordinator to support multi-center health services research studies.

The role involves mentoring staff, coordinating with investigators and funders, organizing study data, and ensuring regulatory alignment across sites. Strong leadership, project management, and IRB familiarity are essential.

Qualifications

• Bachelor's degree required.
• 2-4 years direct experience in health services research.
• Master's degree preferred.
• Experience with IRB submissions preferred.

Responsabilités

• Maintain operation center regulatory files and ensure regulatory compliance.
• Attend regular meetings with investigators and senior staff; coordinate data, reports, and summaries.
• Contribute to study form/SOP design, materials, recruitment, data collection, databases, equipment orders, and budget tracking.

Connaissances

IRB experience

Regulatory knowledge

Data collection

Leadership

Project management

English proficiency

Formation

Bachelors Degree

Master's degree preferred

Description du poste

Position Summary

*As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role when Hired for NYC Offices

Title: Senior Research Coordinator

Location: Upper East Side

Org Unit: Arnab Ghosh Research

Weekly Hours: 35.00

Exemption Status: Exempt

Salary Range: $81,500.00 - $90,100.00

*As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role when Hired for NYC Offices

Working closely with the Principal Investigator, the Senior Research Coordinator (SRC) will provide senior level support for the implementation, coordination, and monitoring of multi-center health services research studies. This includes mentorship of lower-ranking research staff; liaising with internal and external collaborators, including research staff, investigators, and funders; as well as the organization of study data throughout the research process.

Job Responsibilities

• Assists with maintenance of operation center regulatory files, and ensuring compliance with regulatory agencies. Oversees study inventory, including acquisition and disposal of study-related materials.
• Attends meetings regularly with investigators and senior staff. Coordinates preparation of data, reports and meeting summaries.
• Provides input on: design of study forms/standard operating procedures, participant information materials, recruitment of study participants, data collection, creation of databases, ordering equipment, and research account monitoring.
• Is proficient with implementing existing statistical analysis code. Assists with training junior research staff in implementing statistical analysis code.
• Acts as lead contact person for new and on-going research projects. Supervises the implementation of research studies in the field. Provides logistical support for multi-site research projects. This may include coordinating other SRC’s work.
• Explains to participants study details and provides relevant materials. Obtains informed consent and acquires interview recordings/data as required by the protocol(s). Ensures good Clinical Practices compliance and mentors less experienced research staff.
• Tracks and reports progress of data collection, data entry, and data cleaning to the Principal Investigator. Maintains and protects confidential research data.
• Assists in preparation/submission of grant proposals/applications. Mentors less experienced research staff on IRB applications and other regulatory requirements. Liaises with Research Ethics Board, funding agencies and external collaborators.
• Ensures compliance with protocol guidelines and requirements of regulatory agencies. Contributes to revising current SOPs and writing new SOPs.
• Works directly with Investigators to prepare dissemination materials (e.g., manuscripts; abstracts, presentations, and posters for meetings).
• Provides agenda, minutes, and action items for meetings.
• Performs other job-related duties as required.

Education

• Bachelor's Degree

Experience

Master's degree is preferred.

2 - 4 years direct experience in health services research. Experience with IRB submissions preferred.

Knowledge, Skills and Abilities

• Experience with conducting and carrying out protocols and research coordination.
• Familiarity with IRB interaction, regulatory policies, database input and report generation.
• Research experience in an academic health center with exposure to a team research environment at all levels (senior investigators, nurses, research coordinators, lab technicians).
• Demonstrated leadership skills and ability to mentor others.
• Strong project management skills.
• Proficiency (written and spoken) in English.