Więcej informacji
- Numer referencyjny 53/03/2025
- Lokalizacja W Polsce
- Forma wykonywanej pracy praca hybrydowa
- Wymiar czasu pracy część etatu
- Wymagany poziom doświadczenia Brak
- Wymagany poziom doświadczenia student
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Wymagania
Deadline to apply 31st of March
Requirements:
- Education in biological sciences or a healthcare-related field
- Effective communication in English
- Attention to detail
- Analytical skills
- Time management and prioritization skills
- Collaboration skills
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Poszukiwane kompetencje
Fluent English
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Zakres obowiązków
Global Clinical Solutions (GCS) drives the delivery of services and technology for AstraZeneca for its internal and external stakeholders.We are looking for interns to join our TQC and SFD teams, each offering unique opportunities to engage in critical quality and compliance activities.TQC Team:The Technical Quality Check (Tech QC) team is dedicated to maintaining the highest standards of document quality and compliance. Interns will have the opportunity to participate in the meticulous review process of eTMF documents within the Veeva Clinical Vault (VCV) system. Under the guidance of experienced professionals, they will learn to perform thorough quality checks and controls, ensuring adherence to Good Documentation Practice and compliance with rigorous regulatory standards. This role emphasizes the importance of document integrity, accuracy, and the seamless management of compliant processes.SFD Team:The SFD team focuses on performing Technical Quality Checks of documents stored in the eTMF. Interns will be involved in cross-referencing these documents with site personnel lists obtained from the CTMS, identifying discrepancies and errors, and providing support in resolving these discrepancies. This experience will develop interns' analytical skills and enhance their ability to manage and verify critical documentation. Through these activities, interns will gain insight into effective document management and the importance of meticulous cross-checking to maintain data accuracy.Joining either team provides a valuable learning experience and plays a vital role in supporting our mission of achieving excellence in document quality and regulatory compliance.
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Oferowane warunki zatrudnienia
All interns will:
- Undergo role-specific training and will be mentored by highly experienced professionals.
- Learn about AstraZeneca and a global pharmaceutical company work environment.
- Undertake real work, proactively collaborating with our experienced staff.
At the end of your internship you will receive a certificate and feedback from the team; many of our interns are successful applicants for permanent roles within our global clinical research centre!
The internships will start in July and last from 3 months.
We work in a hybrid scheme, be prepared to work partially office based.
Don’t miss your opportunity! We are waiting for you!
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