Regulatory Affairs Euros Full Time Permanent jobs
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Found 79 jobs
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Senior Regulatory Affairs Lead - CTA
We are currently looking for Senior Regulatory Affairs Lead (Consultant) with experienced in Clinical Trail Applications (CTAs) under EU-CTR direct...
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Regulatory Affairs Consultant
We are looking for a Regulatory Affairs Professional to join our team in Poland and work on a client dedicated project. This role can be home or of...
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Senior Regulatory Affairs Associate (CTA)
We are looking for a Senior Regulator y Affairs Associate to join our growing team in Romania. This role can be either home or office based in Bu...
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Senior Site Activation Specialist, Regulatory Expert
Senior Site Activation Coordinator, Regulatory Specialist Country Site ActivationJoin us on our exciting journey!IQVIA’s Country Site Activatio
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Director Regulatory Strategy, CMC, Germany - L
CROMSOURCE is a growing international CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focuse...
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Regulatory Affairs Specialist - Spain
Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and
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Regulatory Affairs Specialist- Quality Assurance
"IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for pat
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RA Scientist - NEW
Thornshaw Scientific, in collaboration with my client, a global pharmaceutical company, now have a new opportunity for an RA Scientist.
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Regulatory Affairs Officers - Dublin
Thornshaw Scientific, in collaboration with my client, a global pharmaceutical company, now have a new opportunity for a Regulatory Affairs Officer.
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Senior/Specialist, Regulatory Affairs - Poland - Home/Office-Based
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent dise
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Senior Global Regulatory Affairs Specialist
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research provid
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Publishing Specialist
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission
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Safety & PV Submission Specialist (Submissions to the Local Regulatory Agency experience required)
Safety & Pharmacovigilance Submissions Specialist I Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to ...
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Senior Manager Regulatory Affairs
As part of our global expansion, we are now looking to fill an important role in our regulatory affairs function. This newly created role in EU/Int...
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Chargé(e) d'Affaires Réglementaires - Avignon - CDI
Rejoignez une entreprise à dimension humaine de 17 collaborateurs, où les opportunités s'étendent bien au-delà des frontières. Vous serez au cœur des
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SSU & Regulatory Specialist I
Site Start-Up & Regulatory Specialist I Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate c...
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Regulatory Affairs Specialist, Belgium - P
CROMSOURCE is searching for a Regulatory Affairs Specialist to join one of our clients, one of the most innovative pharmaceutical companies in the ...
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Executive CMC Consultant | Permanent | Relocation Included!
As a Regulatory CMC Consultant, you will be part of an elite team that sets the industry standard for excellence. Collaborating with top-tier professi
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Manager, Global Regulatory Submissions (Remote)
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortre...
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Biometrics Manager, Belgium - S
CROMSOURCE flexible resourcing department, is currently working with one of our partner sponsors to hire a Biometrics Manager , to join their team ...