Senior Research Data Coordinator for Clinical Trials & EMR

Moffitt Cancer Center; United States; Remote; USD 31,000 - 48,000; Full time

Job summary

Moffitt Cancer Center in Florida seeks a Research Database Coordinator III to manage protocol-specific data for diverse oncology trials. You will extract data from medical records, EMR, pathology and radiology reports, ensuring alignment with GCP and sponsor requirements.

This senior role requires independent work, strong communication with study teams, and meticulous data quality control, with the ability to handle high volume and complex datasets across multiple trials.

Qualifications

• Experience with clinical trial management systems and EMR.
• Ability to interpret and extract data from complex medical records.
• Strong written and verbal communication; able to train others if needed.

Responsibilities

• Review and extract trial data from medical records, clinic notes, reports and questionnaires.
• Ensure data quality, integrity and alignment with GCP and protocol requirements.
• Collaborate with study coordinators, monitors and data managers; resolve data queries.
• Maintain confidentiality and security of subject data while working independently.

Skills

EMR experience

Clinical trial systems

Communication skills

Independent work

Education

HS diploma/GED + 4 yrs data management

Associate degree + 2 yrs data management

Tools

EMR systems

CTMS

Job description

Moffitt Cancer Center in Florida seeks a Research Database Coordinator III to manage protocol-specific data for diverse oncology trials. You will extract data from medical records, EMR, pathology and radiology reports, ensuring alignment with GCP and sponsor requirements.

This senior role requires independent work, strong communication with study teams, and meticulous data quality control, with the ability to handle high volume and complex datasets across multiple trials.