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AbbVie
The Senior Manager, Data Standards leads the development and governance of clinical data standards for AbbVie's clinical trials.
Weekday AI
As a Regulatory Affairs Specialist, you will ensure medical technologies meet regulatory requirements for global markets.
AbbVie
The Senior Analyst, Data Standards is responsible for developing data and reporting standards for clinical trials at AbbVie, ensuring compliance with CDISC standards.
Invivyd
Invivyd
The Senior Manager, Statistical Programming leads statistical programming efforts for regulatory submissions and ensures data integrity and quality.
Amgen
Join Amgen as a Medical Sciences Director to lead late phase clinical development in oncology and contribute to innovative drug development.
Intercept Pharmaceuticals
The Principal Statistical Programmer supports statistical programming efforts and ensures the integrity of clinical trial data.
Glycomine
The Medical Director will oversee clinical development programs, ensuring the design and execution of clinical trials while providing expert medical oversight.
DELFI Diagnostics
The Staff Systems Engineer will design and develop automated diagnostics for early cancer detection, collaborating with cross-functional teams.
RayzeBio
RayzeBio
The Senior Manager of Biostatistics is responsible for leading statistical analysis and clinical study design while collaborating with cross-functional teams to ensure compliance and quality in regulatory submissions.
Kyverna Therapeutics
Kyverna Therapeutics is seeking a Senior Director of European Regulatory Affairs to lead regulatory strategies and submissions for advanced therapy medicinal products.
Pharmacy
Pharmacy
Seeking a Pharmacovigilance & Drug Safety Specialist (PharmD) to analyze safety data and prepare regulatory submissions.
RayzeBio
RayzeBio
The Associate Director, Biostatistics is responsible for leading the statistical aspects of clinical trials and contributing to the overall drug development strategy.
RayzeBio
RayzeBio
The Associate Director of Biostatistics will lead statistical support for clinical trials and contribute to the drug development process.
Ergomed
Join Ergomed as a Clinical Research Associate II, where you'll monitor clinical studies in oncology and rare diseases, requiring proficiency in English and French.
Aidoc
Join Aidoc as a Senior Clinical Research Manager to enhance the clinical credibility of AI in radiology.