Explore 10 Remote Fda Submissions Jobs
The Senior Regulatory Affairs Manager - Oncology will lead regulatory support for IVD/CDx products, managing FDA submissions and ensuring compliance throughout the product lifecycle.
The Vice President, Product Software will lead the product technology lifecycle and ensure compliance for regulated software products in the medical device industry.
P.T
Partner Therapeutics
The Vice President, Regulatory Affairs is responsible for leading the regulatory strategy and compliance efforts at Partner Therapeutics.
The Director of Biostatistics leads statistical support for clinical studies, ensuring integrity and compliance with regulatory standards.
The Senior Clinical Project Manager will lead clinical research projects at Treace, focusing on strategy, execution, and budget management.
Seeking a Manager/Senior Manager of Regulatory Affairs to lead global regulatory strategies and submissions for medical devices.
Tempus is looking for a Director of Regulatory Affairs to lead regulatory strategies for medical devices and ensure compliance with global regulations.
Join Prenuvo as an MRI Radiologist - Director of AI to lead AI model development and ensure regulatory compliance while performing clinical radiology.
The Senior Clinical Research Scientist will lead clinical research activities focused on peripheral nerve science and ensure regulatory compliance.
The Senior Clinical Research Scientist will lead clinical research activities focused on peripheral nerve science and ensure regulatory compliance.
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