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작업 내용
Job description
Key accountabilities
- Ensure the study site is compliant with all local and federal laws and regulations
- Monitor study sites and activities to ensure the appropriate industry protocols and terms of the study are being followed
- Providing clinicians with instructions on how to conduct the trials
- Writing drug trial methodologies
- Collecting and authenticating data collection forms
Benefits
- Uitdagende projecten in lijn met jouw interesses en talenten
- Persoonlijke opvolging en open communicatie zowel voor als na indiensttreding
- Mogelijkheid tot het volgen van extra opleidingen
- Inspirerende netwerkevents en legendarische afterwork drinks
- Sterk netwerk van toonaangevende klanten
- Expertise binnen IT, Engineering en Life Sciences
- Een vliegende start voor elke junior, verdere groei en kennisdeling voor onze seniors
- Challenging projects based on your interests and skills
- Personal follow-up and clear, transparent communication both before and after commencement of employment
- Possibility to follow extra training
- Inspiring network events and legendary after work drinks
- Strong network of industry leading clients
- Expertise within IT, Engineering and Life Sciences
- A flying start for every junior, growth opportunities and possibility to share gathered knowledge for more senior employees
- Un package salarial attractif avec de nombreux avantages extra-légaux
- Un suivi clair et personnalisé, une communication transparente autant durant la période de recrutement qu’une fois l’entrée effective en poste
- La possibilité de suivre des formations
- Divers événement vous permettant de développer votre réseau et des afterwork drinks légendaires
- Un réseau puissant de clients, leaders dans leur domaine
- Une expertise dans les domaines de l’informatique, de l’ingénierie et des sciences de la vie
- Un tremplin vers une évolution rapide pour les juniors et la possibilité de partager des connaissances acquises pour nos employés plus seniors
Have you got what it takes?
Skills, Knowledge and Experience
- Bachelor’s degree in biological science or a related field.
- 2+ years of experience as a Clinical Research Associate.
- Knowledge of the pharmaceutical industry, terminology, and practices.
- Knowledge of GCP-ICH
Reference number: 36977
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마감 시간: 31-12-2025
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작업 보고
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