RemoteOtterRemoteOtterExplore 220 Remote Regulatory Submissions Jobs
M.M
Mind Medicine
Definium Therapeutics is seeking an Associate Director of Medical Writing to author clinical and regulatory documents and support clinical study execution.
Sobi
The Director of Project Management at Sobi will lead strategic initiatives for the launch of pharmaceutical products, ensuring effective project management and cross-functional collaboration.
B.F.S
BeiGene France Sarl
The Associate Director, Scientific Programming will lead statistical programming efforts for oncology projects, ensuring regulatory compliance and high-quality deliverables.
SerenaGroup
SerenaGroup
SerenaGroups is looking for a Medical Writer to create clear and engaging content from complex medical information.
A.T.P
Axiom Talent Platform
Seeking an experienced FDA Regulatory Attorney with expertise in Class III IVD and companion diagnostics.
Pfm
The Start Up Lead oversees global site start-up activities and ensures effective execution of site start-up strategies.
Precisionmedicinegroup
The Start Up Lead is responsible for overseeing global site start-up activities and ensuring timely delivery of project milestones.
Sionna Therapeutics
Sionna Therapeutics is seeking a Senior Director of Clinical Pharmacology to lead clinical pharmacology initiatives and support drug development programs.
Precision Medicine Group
Join Precision for Medicine as a Clinical Research Associate I/II, working remotely with a focus on oncology studies in Belgium or the Netherlands.
Dianthus Therapeutics
The Associate Director, Medical Writing will lead the development of clinical and regulatory documents in a fully remote role.
DeepHealth
The Program Manager will oversee AI initiatives, managing cross-functional teams and ensuring alignment with business objectives.
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 Associate, Study Management III is responsible for leading global clinical trials and ensuring efficient execution in compliance with quality standards.
PTF Consulting
The Manager, Medical Writing leads complex medical writing projects to support regulatory submissions and compliance.
AbbVie
The Medical Writing Coordinator/Publisher II is responsible for coordinating and publishing clinical study reports and ensuring compliance with regulatory documentation standards.