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Contract) eTMF Specialist (m/f)
Eingestellt von Red - The Global SAP Solutions Provider
Gesuchte Skills: Support, Client
Projektbeschreibung
(Contract) eTMF Specialist (m/f)
Zurich, Switzerland
TYPE: Contract
START DATE: 02/01/2018
END DATE: 01/07/2018
DURATION: 6 months with possible extension
LOCATION: Zurich
CLIENT INDUSTRY: Pharmaceutical
LANGUAGE: EnglishProject Highlights:
- Support the development delivery functions with tasks related to the eTMF quality control and maintenance
- Provide guidance on the eTMF process and practical support on how to use the system
- Follow up with the internal and vendor functions on the eTMF quality issues until their resolution
Requirements:
- Bachelor degree or equivalent, preferably in life science, clinical research, or related discipline
- Comprehensive practical knowledge of TMF processes, related standards (eg DIA Reference Model) and its quality control
- Thorough understanding of ICH-GCP quality standards and other relevant regulations
- 5 years of clinical trial experience in the pharmaceutical industry or university hospital
- of 3 years' experience with the eTMF
- IT literacy, proficiency with Microsoft Office applications as well as practical experience with the electronic Trial Master File
- Proactive working style in combination with very good communication skills
Zurich, Switzerland
TYPE: Contract
START DATE: 02/01/2018
END DATE: 01/07/2018
DURATION: 6 months with possible extension
LOCATION: Zurich
CLIENT INDUSTRY: Pharmaceutical
LANGUAGE: EnglishProject Highlights:
- Support the development delivery functions with tasks related to the eTMF quality control and maintenance
- Provide guidance on the eTMF process and practical support on how to use the system
- Follow up with the internal and vendor functions on the eTMF quality issues until their resolution
Requirements:
- Bachelor degree or equivalent, preferably in life science, clinical research, or related discipline
- Comprehensive practical knowledge of TMF processes, related standards (eg DIA Reference Model) and its quality control
- Thorough understanding of ICH-GCP quality standards and other relevant regulations
- 5 years of clinical trial experience in the pharmaceutical industry or university hospital
- of 3 years' experience with the eTMF
- IT literacy, proficiency with Microsoft Office applications as well as practical experience with the electronic Trial Master File
- Proactive working style in combination with very good communication skills
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Sonstiges