Clinical Data Coordinator for Cancer Research

US Oncology Inc.; Daphne (AL); On-site; USD 42,000 - 62,000; Full time

Job summary

Southern Cancer Center in Daphne, AL is seeking a Data Coordinator to join our Research Team. You will ensure clinical trial data is accurate, complete, and on time, serving as a behind-the-scenes powerhouse that keeps the study moving.

Ideal candidates have a high school diploma, 0-3 years of experience in medical office settings, oncology experience preferred, strong attention to detail, and proficiency with MS Office and databases. HIPAA compliance a must.

Qualifications

• High School Diploma required.
• Associate's degree preferred; Bachelor's a plus.
• 0-3 years of experience.
• Medical office experience required (oncology experience preferred).
• Clinical research experience is a bonus.

Responsibilities

• Capture and enter patient visit data into case report forms (CRFs) with precision.
• Ensure timely data submission in line with USOR SOPs.
• Track, manage, and resolve data queries.
• Collaborate with clinical staff and research leadership to address data concerns.
• Maintain research records and patient tracking tools in our clinical trial management system.
• Keep all documentation compliant with HIPAA and confidentiality requirements.
• Prepare for and support sponsor monitoring and audit visits.
• Help with scheduling follow-ups and protocol-related patient visits.
• Assist with research supply management.
• Support specimen, imaging, and research material collection/processing.

Skills

Detail-oriented

Organizational skills

Multitasking

Communication

MS Office

Medical terminology

Education

High School Diploma

Associate's degree

Bachelor's degree

Tools

Databases

MS Office

Job description

Southern Cancer Center in Daphne, AL is seeking a Data Coordinator to join our Research Team. You will ensure clinical trial data is accurate, complete, and on time, serving as a behind-the-scenes powerhouse that keeps the study moving.

Ideal candidates have a high school diploma, 0-3 years of experience in medical office settings, oncology experience preferred, strong attention to detail, and proficiency with MS Office and databases. HIPAA compliance a must.