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Clinical Protocol Coordinator at Axle - ApplyBlast

Clinical Protocol Coordinator

Axle

10 days ago

3.6 on Glassdoor

Bethesda, Maryland, United States

Onsite

Full Time

Senior

0 applicants

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About this role

The Clinical Protocol Coordinator independently supports the Division of Intramural Research, Clinical Trials Unit at NINDS by providing regulatory and operational coordination throughout the clinical research protocol lifecycle. This role involves preparing regulatory documentation, maintaining study records, tracking safety reporting, and coordinating monitoring activities to empower decision-making and accelerate research discoveries. The position requires expertise in clinical trial management, IRB requirements, and collaboration with research staff and oversight entities.

Responsibilities

Coordinate regulatory and operational activities throughout the clinical research protocol lifecycle
Prepare and submit regulatory documentation including IRB submissions, amendments, and safety reports
Maintain audit-ready regulatory files and track study status, approvals, and monitoring activities

Skills

Qualifications

Master's degree

About Axle

axleinfo.com

Headquarters

Rockville, Maryland, United States

Company Size

501-1000 employees

Founded

2002

View Profile

Axle is a bioscience, technology, and research solutions company focused on accelerating biomedical discovery. They provide innovative technology platforms and collaborative research services, partnering with prominent organizations such as the NIH to support translational research and scientific advancement. Guided by the tagline "Advance. Accelerate. Achieve.", Axle aims to empower breakthroughs in biomedical research through technical expertise and strategic partnerships.