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Duke Careers
Overview
The Regulatory Coordinator will manage regulatory operations for complex oncology studies, ensuring compliance and audit readiness. This includes preparing and submitting necessary documentation and coordinating study management activities.
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Compensation
$59,829 - $99,960 / YEAR
Posted
15 days ago
The US Oncology Network
Responsible for managing research regulatory and administrative activities for clinical trials, including site qualification and document management. Collaborates with investigators and central operations to ensure compliance with SOPs, GCP, and federal regulations.
Salary not listed
25 days ago
Medical University of South Carolina
The coordinator manages pre-award grant processes, including budget development and proposal submission. They also ensure regulatory compliance by managing IRB documentation and adhering to FDA and GCP requirements.
$37,200 - $59,500 / YEAR
1 month ago
Nationwide Children's Hospital
Assists with administrative components to ensure regulatory compliance for clinical research projects, including maintaining study binders and files. Prepares and submits IRB documents while ensuring accuracy across regulatory and grant systems.
Assists with administrative components to ensure regulatory compliance for clinical research projects. Responsibilities include maintaining study binders, submitting IRB documents, and collecting investigator credentials.
Cedars-Sinai
The Regulatory Coordinator prepares and submits clinical trial protocols and supporting documentation to various regulatory bodies and committees. They ensure ongoing compliance with federal and local regulations, including FDA and IRB requirements, while maintaining accurate research files.
$34 - $58 / HOUR
RCCA MSO LLC
The Regulatory Coordinator Assistant is responsible for preparing, compiling, and submitting regulatory documents for clinical trials while ensuring compliance with FDA and IRB regulations. They also manage site documentation, coordinate monitoring visits, and address inquiries from sponsors and clinical trial teams.
$27 - $37 / HOUR
3 months ago
OKLAHOMA CANCER SPECIALISTS MANAGEMENT COMPA
Coordinates the research and administrative activities of clinical trials, managing regulatory procedures. Provides regulatory and safety support services in compliance with relevant guidelines.
4 months ago
