Clinical Research Associate @ OneOncology
Your Application Journey
Email Hiring Manager
Job Details
About OneOncology
OneOncology is positioning community oncologists to drive the future of cancer care through a patient-centric, physician-driven, and technology-powered model. Our team collaborates with industry leaders in oncology, technology, and finance to improve the lives of everyone living with cancer.
Role Overview
The Clinical Research Associate supports clinical research across the OneOncology Research Network (OneR). Reporting to the Manager, Research Quality, this role evaluates clinical trial data and records for compliance with FDA regulations, GCP guidelines, and quality standards.
Key Responsibilities
- Conduct quality control activities at network sites.
- Review source records, data, and regulatory documentation for compliance.
- Document nonconformities and follow up with corrective actions.
- Track findings and prepare periodic reports for stakeholders.
- Support audit, inspection-readiness and SOP development.
Key Competencies & Qualifications
Minimum of 2 years’ experience in clinical research with strong attention to detail, analytical capabilities, and excellent communication skills. Familiarity with FDA regulations, GCP guidelines, and proficiency in Microsoft Office. Experience with electronic data capture systems and electronic medical records (OncoEMR and Florence eBinders are a plus) is desired. A Bachelor’s degree is required and SOCRA or ACRP certification is preferred.
Key skills/competency
Clinical Trials, Quality Control, Compliance, FDA, GCP, Data Integrity, Auditing, Reporting, Process Improvement, SOP
How to Get Hired at OneOncology
🎯 Tips for Getting Hired
- Research OneOncology's culture: Review mission and recent news on their site.
- Customize your resume: Highlight clinical research and compliance skills.
- Showcase attention to detail: Include examples of data review experience.
- Prepare for interviews: Practice questions on quality control procedures.