Clinical Research Data Coordinator - Multi-Site Trials

Medix; Town of Florida (NY); On-site; USD 52,000 - 76,000; Full time

Job summary

Medix is seeking a Clinical Research Data Coordinator to support a growing multi-site clinical research team in South Florida. The role focuses on accurate data management, electronic systems support, and day-to-day data operations across trials.

Ideal candidates have experience in clinical research or healthcare data entry, with familiarity of Medidata Rave or REDCap preferred and exposure to E-Reg, eSource, and CTMS platforms. Travel between sites may be required.

Qualifications

• Previous experience in clinical research, clinical trials, or healthcare data entry.
• Experience with clinical research databases and electronic systems.
• Experience with Medidata Rave and/or REDCap strongly preferred
• Familiarity with E-Reg, eSource, and CTMS platforms
• Strong attention to detail and organizational skills
• Ability to manage multiple priorities in a fast-paced research environment
• Strong computer and data entry skills
• Ability to work independently while collaborating effectively with a research team

Responsibilities

• Perform accurate and timely data entry for clinical research studies
• Enter and maintain study data in electronic systems and databases
• Support clinical research teams with data collection, tracking, and reconciliation
• Work with Electronic Regulatory (E-Reg), eSource, and CTMS systems
• Review data for accuracy, completeness, and consistency
• Assist with resolving data discrepancies and maintaining data quality
• Support multiple clinical research sites as needed
• Collaborate with Clinical Research Coordinators, Research Assistants, and other study personnel
• Maintain confidentiality and follow applicable research, regulatory, and site-specific procedures
• Travel between research locations as needed to support data-related activities

Skills

Data entry

Attention to detail

Independent work

Team collaboration

Tools

Medidata Rave

REDCap

E-Reg

CTMS

Job description

Medix is seeking a Clinical Research Data Coordinator to support a growing multi-site clinical research team in South Florida. The role focuses on accurate data management, electronic systems support, and day-to-day data operations across trials.

Ideal candidates have experience in clinical research or healthcare data entry, with familiarity of Medidata Rave or REDCap preferred and exposure to E-Reg, eSource, and CTMS platforms. Travel between sites may be required.