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Senior Data Engineer Data Factory

Schiphol Group - Schiphol
the overall airport experience. The Central Data Factory team is known for its strong collaboration with various departments. We create robust data pipelines that ensure data integrity and safety , contributing to a data-driven
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Operator Drug Products

Luba - Amsterdam
Vacaturebeschrijving Word operator in de farmaceutische sector in Amsterdam. Bedien geavanceerde machines en lever een bijdrage aan levensreddende medicijnen!Over het werk Als operator speel je een cruciale rol in het product
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Coördinator Quality, Health, Safety & Environment bi...

Yacht - Almere
Bedrijfsomschrijving Onze opdrachtgever, Antalis, is onderdeel van de Kokusai Pulp & Paper Group (Japan). In Europa en Latijns-Amerika is Antalis een Bedrijfsomschrijving Onze opdrachtgever, Antalis, is onderdeel van de Kokus
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Senior Clinical Data Manager

Oxfordcorp
data coding and safety reviews as needed; Contribute towards process improvement, data standards and efficiency gaining initiatives within data management working with data management leadership as needed; Be
 60+ dagen geleden - Preview - Opslaan

Clinical Data Manager

Oxfordcorp
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

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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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
CONTRACTOR - Preview - Opslaan

Study Start-Up Specialist

Oxfordcorp
Specialist supports drug label preparation and approval (as local label representative) for studies in collaboration with local Regulatory/Quality department, as required The Study Start-Up Specialist liaises and collaborates
 60+ dagen geleden - Preview - Opslaan

Empower your career - a female perspective

Hyphen Projects - Utrecht
are making waves in the Life Sciences! Speakers Liesbeth Hof | Sr Director Project Management Office | AM-Pharma Liesbeth Hof has a Master in Medical Biology with over 20 years of international experiences in the
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Clinical Research Regulatory Coordinator

Oxfordcorp
clinical pharmacology principles, with ability to review emerging safety and efficacy profile of a drug candidate and recognize potential serious adverse effects;Demonstrated understanding of the complexities and recent developments
 60+ dagen geleden - Preview - Opslaan

(Junior) Clinical Trial Assistant EN or FR/EN or FR/EN)

Oxfordcorp
Do you actively want to contribute supporting drug development, in one of the biggest biotech companies, with an amazing pipeline? Then this job as Clinical Trial Assistant might be for you ! Job Description As a
 60+ dagen geleden - Preview - Opslaan

Epidemiologist

Epidemiologie
medical writers, safety and pharmacovigilance specialists, project managers and office support staff spread over more than 10 countries. Our headquarters are in Leuven, Belgium but all of our staff work remotely. You may
 60+ dagen geleden - Preview - Opslaan
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