Clinical Research Data Specialist - Oncology Trials

Moffitt Cancer Center; Tampa (FL); On-site; USD 32,000 - 48,000; Full time

Job summary

Moffitt Cancer Center is seeking a Research Data Coordinator II to autonomously review medical records and extract trial data per protocols. You will handle data requirements, ensure compliance with GCP and federal regulations, and collaborate with study coordinators and monitors.

The role supports higher volume and complexity with career growth opportunities in the RDC path. Responsibilities include data capture, query resolution, and contributing to protocol-specific data sets across multiple

Qualifications

• Requires high attention to detail and the ability to synthesize information from medical records.
• Must understand and interpret components of the medical record and maintain confidentiality.
• Experience with data management in clinical/research settings preferred.

Responsibilities

• Review and synthesize information from medical records to extract trial data as per protocols.
• Ensure data requirements align with good clinical practice and federal regulations.
• Collaborate with study coordinators and monitors; assist with higher patient volume or trial complexity.

Skills

Verbal communication

Written communication

Interpersonal skills

Prioritization

Independent work

Confidentiality

Medical records interpretation

Education

High School Diploma/GED

AA/AS degree + 1 year data management

Tools

Powerchart

OnCore

Data entry systems

Job description

Moffitt Cancer Center is seeking a Research Data Coordinator II to autonomously review medical records and extract trial data per protocols. You will handle data requirements, ensure compliance with GCP and federal regulations, and collaborate with study coordinators and monitors.

The role supports higher volume and complexity with career growth opportunities in the RDC path. Responsibilities include data capture, query resolution, and contributing to protocol-specific data sets across multiple