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Clinical Trial Associate
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Client, Adobe
Projektbeschreibung
Clinical Trial Associate wanted for our Basel based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- At least 2 years' experience of supporting electronic document management systems and publishing tools
- Working experience in document publishing and document management including Microsoft office applications, Documentum, Adobe Acrobat, ISI toolbox and ISI publisher
- Basic experience in non-clinical and clinical report preparation and submission
- Constitutive knowledge of regulatory requirements and pharmaceutical development
- Familiarity with GxPs and OECD regulations
- Languages: fluent English both written and spoken
YOUR TASKS:
- Supporting global users in use of word processing, electronic publishing and document management systems
- Troubleshooting and providing solutions to basic technical and process issues
- Assisting users with basic technical issues
- Conducting basic document issue resolution with customers and collaborators
- Maintaining basic knowledge of current systems standards, regulatory guidelines and legal requirements
START: 02/2017
DURATION: 10MM+
LOCATION: Basel, Switzerland
REF.NR.: BH10423
Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a contact telephone number.
DUE TO WORK PERMIT RESTRICTIONS WE CAN UNFORTUNATELY ONLY CONSIDER APPLICATIONS FROM EU OR SWISS CITIZENS AS WELL AS CURRENT WORK-PERMIT HOLDERS FOR SWITZERLAND.
GOING THE EXTRA MILE
NEW TO SWITZERLAND? In case of successful placement, we support you with:
- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more
YOUR EXPERIENCE/SKILLS:
- At least 2 years' experience of supporting electronic document management systems and publishing tools
- Working experience in document publishing and document management including Microsoft office applications, Documentum, Adobe Acrobat, ISI toolbox and ISI publisher
- Basic experience in non-clinical and clinical report preparation and submission
- Constitutive knowledge of regulatory requirements and pharmaceutical development
- Familiarity with GxPs and OECD regulations
- Languages: fluent English both written and spoken
YOUR TASKS:
- Supporting global users in use of word processing, electronic publishing and document management systems
- Troubleshooting and providing solutions to basic technical and process issues
- Assisting users with basic technical issues
- Conducting basic document issue resolution with customers and collaborators
- Maintaining basic knowledge of current systems standards, regulatory guidelines and legal requirements
START: 02/2017
DURATION: 10MM+
LOCATION: Basel, Switzerland
REF.NR.: BH10423
Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a contact telephone number.
DUE TO WORK PERMIT RESTRICTIONS WE CAN UNFORTUNATELY ONLY CONSIDER APPLICATIONS FROM EU OR SWISS CITIZENS AS WELL AS CURRENT WORK-PERMIT HOLDERS FOR SWITZERLAND.
GOING THE EXTRA MILE
NEW TO SWITZERLAND? In case of successful placement, we support you with:
- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Medien/Design