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Deciphera Pharmaceuticals
The Associate Director, Regulatory CMC will lead and execute CMC regulatory activities for clinical drug development at Deciphera.
Deciphera Pharmaceuticals
The Director of Global Medical Writing will lead document strategy and development for complex clinical documents in a dynamic medical writing team.
R.F.S
Regeneron France SAS
The Senior Editor oversees the quality control of regulatory submission documents and collaborates with writing staff to ensure accuracy and adherence to standards.
Veeva Systems
Join Veeva Systems as a Regulatory Operations Product Expert to drive customer success in the life sciences sector.
Welcome to the Tarsanet Internal Career Center!
The Manager I, Regulatory Affairs Operations will oversee regulatory submissions and manage electronic document systems.
Welcome to the Tarsanet Internal Career Center!
The Director, Regulatory Affairs CMC will lead the regulatory strategy for Chemistry, Manufacturing, and Controls.
P.P.M
Praxis Precision Medicines
The Senior Regulatory Submissions Manager will oversee regulatory submissions to ensure compliance and quality.
M.M
Mind Medicine
MindMed is seeking a Senior Medical Writer to author clinical and regulatory documents and support clinical study execution.
Telixus
The Medical Writer will lead the writing process for clinical and regulatory documents at Telix Pharmaceuticals.
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