What are the responsibilities and job description for the Data Coordinator position at The US Oncology Network?
Overview
đ§Ş Join Our Research Team: Data Coordinator (Daphne, AL)
Where details matter, data drives care, and your work truly makes a difference.
Are you someone who loves organization, thrives on accuracy, and gets satisfaction from keeping everything running smoothly? Do you enjoy being the behind-the-scenes powerhouse that keeps a team on track?
If soâwe want you on our Research Team at Southern Cancer Center! đ
Responsibilities
⨠What Youâll Be Doing:
Youâre the go-to person making sure research data is accurate, complete, and on timeâbecause in clinical research, every detail matters.
đ§ What Weâre Looking For:
Someone who is detail-driven, organized, and thrives in a fast-paced, team-oriented environment.
Education & Experience
This role is based in a clinical oncology setting. You may be exposed to typical clinical conditions (including communicable diseases and medical materials), and the role involves a mix of computer work, walking/standing, and occasional lifting.
đŹ Ready to Apply?
If youâre organized, dependable, and passionate about doing meaningful workâweâd love to meet you.
đ§Ş Join Our Research Team: Data Coordinator (Daphne, AL)
Where details matter, data drives care, and your work truly makes a difference.
Are you someone who loves organization, thrives on accuracy, and gets satisfaction from keeping everything running smoothly? Do you enjoy being the behind-the-scenes powerhouse that keeps a team on track?
If soâwe want you on our Research Team at Southern Cancer Center! đ
Responsibilities
⨠What Youâll Be Doing:
Youâre the go-to person making sure research data is accurate, complete, and on timeâbecause in clinical research, every detail matters.
- 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
đ§ What Weâre Looking For:
Someone who is detail-driven, organized, and thrives in a fast-paced, team-oriented environment.
Education & Experience
- High School Diploma required
- Associateâs degree strongly preferred; Bachelorâs a plus
- 0â3 years of experience
- Medical office experience required (oncology experience preferred)
- Clinical research experience is a bonus
- High attention to detail (seriouslyâwe mean it đ)
- Strong organizational and multitasking skills
- Excellent communication (written & verbal)
- Confidence using Microsoft Office and working with databases
- Knowledge of medical terminology
- High level of computer literacy
- Youâll play a direct role in advancing cancer research
- Youâll work alongside a collaborative, mission-driven team
- Every day brings meaningful work that impacts patient care
This role is based in a clinical oncology setting. You may be exposed to typical clinical conditions (including communicable diseases and medical materials), and the role involves a mix of computer work, walking/standing, and occasional lifting.
đŹ Ready to Apply?
If youâre organized, dependable, and passionate about doing meaningful workâweâd love to meet you.