Explore 107 Remote Ectd Submissions Jobs
The Associate Medical Director will oversee scientific content development and support client projects in the medical communications field.
Veeva Systems
Join Veeva Systems as a Product Expert to drive customer success in Regulatory Information Management products within the life sciences sector.
Xcenda
Xcenda
Join Cencora as a Manager of Regulatory Affairs to lead regulatory submissions and support cross-functional teams in the healthcare products industry.
Join Natera as a Senior Program Manager to lead cross-functional teams in launching and improving biotech products.
The Senior Clinical Project Manager will lead clinical research projects at Treace, focusing on strategy, execution, and budget management.
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Centessa Pharmaceuticals
Centessa Pharmaceuticals is looking for an Associate Director/Director of Drug Product to lead formulation development and manage external vendors.
Join Rush Street Interactive as a Regulatory Compliance Coordinator, ensuring adherence to regulatory requirements in a dynamic gaming environment.
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Centessa Pharmaceuticals
Centessa Pharmaceuticals is seeking a Senior Director, Clinical Pharmacologist to lead drug development activities for orexin agonist programs.
Jobgether
Jobgether
The Senior Director, Clinical Pharmacology will oversee clinical pharmacology for drug development, leading teams and ensuring regulatory compliance.
Join Dianthus Therapeutics as a Senior Director of Medical Writing, leading the development of clinical and regulatory documents in a remote role.
Join Precision for Medicine as a Clinical Research Associate (CRA) to monitor and manage clinical studies in oncology with a focus on professional growth and work-life balance.
Join Precision for Medicine as a Clinical Research Associate (CRA) in a remote role based in Australia, focusing on Oncology clinical studies.