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Freelance Global Compliance Officer (ZZP)

Yacht - Utrecht
Global Safety Regulatory Location: Based in Amsterdam. Your responsibilities as Global Compliance Officer are leading a global team of 40+ experts who work together to ensure our brands is protected and promoted by
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Freelance Global Compliance Officer (ZZP)

Yacht - Amsterdam
Global Safety Regulatory Location: Based in Amsterdam. Your responsibilities as Global Compliance Officer are leading a global team of 40+ experts who work together to ensure our brands is protected and promoted by
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Freelance Global Compliance Officer (ZZP)

Yacht - Landsmeer
Global Safety Regulatory Location: Based in Amsterdam. Your responsibilities as Global Compliance Officer are leading a global team of 40+ experts who work together to ensure our brands is protected and promoted by
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Clinical Trial Coordinator

Icon Plc - Amsterdam
A Clinical Research Associate is a professional who contributes to accelerated drug /device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. You Reference 2024
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Clinical Research Coordinator - IQVIA

Apeldoorn bij IQVIA via Jobsonline - Apeldoorn
and safety policies, under the direction and delegation of the Principal Investigator. As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and
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Director, Program Management, Translational & Quanti...

Genmab via Jobsonline - Utrecht
research activities to support Genmab’s products from discovery through clinical development. These activities are primarily driven by scientific leads from Early-/Late-stage Translational Research, Non-Clinical Safety , Diagnostics
INTERN - Opslaan

Research Assistant - IQVIA

Ede bij IQVIA via Jobsonline - Ede
week and is expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety
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Research Assistant - IQVIA

Venlo bij IQVIA via Jobsonline - Venlo
week and is expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety
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Clinical Research Associate

Icon Plc - Amsterdam
A Clinical Research Associate is a professional who contributes to accelerated drug /device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. You Reference 2024
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Warehouse Operator (fixed)

Synthon - Nijmegen
Research and Development & Drug Product Manufacturing Carrer de Castelló, 1, 08830 Sant Boi de Llobregat Barcelona, Spain Job details At Synthon you will have a great experience, in an excellent work environment, and
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Warehouse Operator (temporary)

Synthon - Nijmegen
Research and Development & Drug Product Manufacturing Carrer de Castelló, 1, 08830 Sant Boi de Llobregat Barcelona, Spain Job details At Synthon you will have a great experience, in an excellent work environment, and
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Moldmaker Peachtree City (GA), USA

Igs Gebojagema - Eindhoven
requirements Technical Education 8 – 10 years of relevant work experience Reading technical drawings General Safety Requirements MS Office Competencies we are looking for Collaboration Quality
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Clinical Data Manager

Oxford Global Resources
image handling; Be responsible for coordinating with Medical Affairs organization to facilitate data coding and safety reviews as needed; Contribute towards process improvement, data standards and efficiency gaining
60+ dagen geleden - Preview - Opslaan