Clinical Research Data Coordinator

Medix

Town of Florida (NY)

On-site

USD 52,000 - 76,000

Full time

14 hours ago
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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

Clinical Research Data Coordinator (258803) Sweetwater, Florida
Position Summary

We are seeking a Data Coordinator to support a growing clinical research team across multiple research sites in South Florida. This position will be responsible for maintaining accurate clinical research data, supporting electronic systems, and assisting with the day-to-day data management needs of ongoing clinical trials.

The ideal candidate has prior experience working in a clinical research or clinical trial environment and is comfortable working with electronic research systems and databases.

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
Preferred 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
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