RemoteOtterRemoteOtterExplore 16 Remote Ectd Jobs
I.A
Immunic AG
We are seeking a Senior Consultant to support Medical Writing for NDA submissions, with a focus on clinical pharmacology.
PSI CRO
The Associate Medical Writer will be responsible for creating and reviewing clinical documentation in a remote setting.
AbbVie
Join AbbVie's Strategic Medical Writing Operations Team as a Medical Writing Operations Associate, focusing on high-quality clinical and regulatory documentation.
AbbVie
The Medical Writing Coordinator/Publisher II is responsible for coordinating and publishing clinical study reports and ensuring compliance with regulatory documentation standards.
Deciphera Pharmaceuticals
Join a dynamic Medical Writing team as a Principal Medical Writer, leading the development of clinical and regulatory documents.
C.E
Criterion Edge
Join Criterion Edge as a Pharmaceutical Regulatory Consultant to guide clients through regulatory compliance and strategy.
B.F.S
BeiGene France Sarl
The Senior Associate, Submission Operations role involves coordinating and preparing regulatory submissions to global health authorities.
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.N.B
Regeneron NL B.V
The Senior Editor oversees the quality control of regulatory submission documents and collaborates with writing staff to ensure accuracy and adherence to standards.
Veeva
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.