Explore 25 Remote Ema Jobs
The eTMF Specialist will manage TMF processes for clinical studies, ensuring compliance and quality throughout the study lifecycle.
Join Spyre Therapeutics as a Senior Manager in CMC Regulatory Affairs to lead regulatory submissions and strategy for clinical trials.
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Criterion Edge
Join Criterion Edge as a Pharmaceutical Regulatory Consultant to guide clients through regulatory compliance and strategy.
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argenx BV
Seeking a Senior Director to lead regulatory affairs for a growing biopharmaceutical pipeline focused on autoimmune diseases.
Aniesispharma, LLC is seeking a highly organized Remote Project Manager to lead pharmaceutical development projects.
The ePRO Manager will lead the design and oversight of electronic Patient Reported Outcomes systems in clinical trials.
The Clinical Trial Safety Reporting Administrator ensures the timely and compliant submission of safety reports for clinical trials.
The Vice President of Regulatory Affairs will lead global regulatory strategies and submissions for late-stage biopharma programs in a remote role.
Join ClinChoice as a Global Labeling Lead Consultant, providing strategic support in pharmaceutical labeling while working remotely.
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Parexel International
Join Parexel as a Senior Clinical Research Associate I to manage oncology clinical sites in the Paris region.
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Bill & Melinda Gates Foundation - UK Office
The Senior Officer, Regulatory Affairs will manage grants aimed at optimizing regulatory systems for medical products in low-income countries.
Join Amgen as a Global Regulatory Policy and Intelligence Senior Manager to lead and influence regulatory strategies that impact patient care.
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IMVT Corporation
Immunovant is seeking a Senior Director for Clinical Quality Assurance to lead quality efforts and ensure compliance with global regulations.
Join Syner-G BioPharma Group as a Validation Engineer to ensure compliance and enhance quality systems in life sciences.