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Administrative Expert - Clinical Trial
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Support, Client
Projektbeschreibung
Administrative Expert - Clinical Trial wanted for our Zug based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- Proven Track of Commercial Training, Studies or equivalent
- Working experience in a pharmaceutical environment
- Constitutive knowledge of regulatory requirements and pharmaceutical development
- Languages: fluent English both written and spoken
YOUR TASKS:
- Tracking status of regulatory readiness and collaborating with clinical team to take care of regulatory document packages for IRB/IECs and sites
- Ensuring that appropriate versions of legal documents are used and database is kept current
- Being responsible for contract management with investigators and vendors while collaboration with clinical team
- Providing support for trial budget planning, forecast and accounting as well as tracing process agreements and releasing payments to vendors
- Supporting local trial team with the creating, ordering, and mailing of study tools and shipments
START: 01/2018
DURATION: 12MM+
LOCATION: Zug, Switzerland
REF.NR.: BH12024
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:
- Proven Track of Commercial Training, Studies or equivalent
- Working experience in a pharmaceutical environment
- Constitutive knowledge of regulatory requirements and pharmaceutical development
- Languages: fluent English both written and spoken
YOUR TASKS:
- Tracking status of regulatory readiness and collaborating with clinical team to take care of regulatory document packages for IRB/IECs and sites
- Ensuring that appropriate versions of legal documents are used and database is kept current
- Being responsible for contract management with investigators and vendors while collaboration with clinical team
- Providing support for trial budget planning, forecast and accounting as well as tracing process agreements and releasing payments to vendors
- Supporting local trial team with the creating, ordering, and mailing of study tools and shipments
START: 01/2018
DURATION: 12MM+
LOCATION: Zug, Switzerland
REF.NR.: BH12024
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
-
Kategorie:
IT Entwicklung, Sonstiges