Clinical Research Systems Engineer (CTMS)

Iterative Health; New York (NY); Hybrid; USD 32,000 - 55,000; Full time

Benefits offered by this job

Hybrid work environment

Medical, dental, vision

Unlimited PTO

Wellness stipend

401(k) company match

Lunch benefit

Job summary

Iterative Health in New York is seeking a Clinical Research Systems Specialist to strengthen our CTMS-driven operations and study materials. You will ensure accurate configurations, support trial workflows, and partner with cross-functional teams to execute trials efficiently and in compliance.

Ideal candidates bring hands-on clinical research experience, CTMS platform knowledge, and a detail‑oriented approach to quality assurance, documentation, data integrity, and timely study Start-Up across

Qualifications

• Prior experience as a Clinical Research Coordinator (CRC) or in a comparable clinical research operations role.
• Experience working with CRIO, RealTime CTMS, or similar clinical research technology platforms.
• Strong understanding of clinical research workflows and ability to read and interpret clinical trial protocols.
• Exceptional attention to detail and strong quality control.
• Proficiency with Microsoft Office and web-based applications.

Responsibilities

• Build and maintain studies within CTMS platforms reflecting protocols and sponsor requirements.
• Support clinical research sites in CTMS usage and troubleshoot issues.
• Collaborate with cross-functional teams to support study launch and execution.
• Perform quality control reviews and UAT of study builds prior to launch.
• Read, interpret clinical trial protocols and translate requirements into system configurations.
• Maintain databases, trackers, and documentation monitoring activities.

Skills

Clinical Research

CTMS platforms

Data management

Regulatory knowledge

Microsoft Office

Education

Associate degree or equivalent

Tools

CRIO

RealTime CTMS

CTMS

Job description

Iterative Health in New York is seeking a Clinical Research Systems Specialist to strengthen our CTMS-driven operations and study materials. You will ensure accurate configurations, support trial workflows, and partner with cross-functional teams to execute trials efficiently and in compliance.

Ideal candidates bring hands-on clinical research experience, CTMS platform knowledge, and a detail‑oriented approach to quality assurance, documentation, data integrity, and timely study Start-Up across