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Clinical Trial Associate
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Support, Client
Projektbeschreibung
Clinical Trial Associate wanted for our Zug based client in the pharmaceutical industry.
YOUR EXPERIENCE/SKILLS:
- Bachelor degree in corresponding field
- Previous work experience in a relevant position together with knowledge in the clinical research environment
- Good organizational skills to effectively prioritize workload coupled with the ability to work under pressure
- Competence to work in a Matrix organization along with flexibility and collaboration skills
- Languages: fluent English both written and spoken, German or French is a plus
YOUR TASKS:
- Collaborating with CRAs and TMo team as well as providing support in Ethics Committee submission process
- Maintaining the Trial Master File and Investigator Folder including scanning, uploading trial documents to the document management system and ensuring medical writing as well as translating of clinical study documents
- Supporting the TMo team in ordering, tracking and coordinating shipment of any necessary trial supplies or study tools as well as in endpoint tracking or other specific tracking needs
- Ensuring that the reporting systems are kept up to date
- Organizing meetings with local Investigator, webcasts, TCs or other meeting formats
START: ASAP
DURATION: 12MM+
LOCATION: Zug, Switzerland
REF.NR.: BH12661
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:
- Bachelor degree in corresponding field
- Previous work experience in a relevant position together with knowledge in the clinical research environment
- Good organizational skills to effectively prioritize workload coupled with the ability to work under pressure
- Competence to work in a Matrix organization along with flexibility and collaboration skills
- Languages: fluent English both written and spoken, German or French is a plus
YOUR TASKS:
- Collaborating with CRAs and TMo team as well as providing support in Ethics Committee submission process
- Maintaining the Trial Master File and Investigator Folder including scanning, uploading trial documents to the document management system and ensuring medical writing as well as translating of clinical study documents
- Supporting the TMo team in ordering, tracking and coordinating shipment of any necessary trial supplies or study tools as well as in endpoint tracking or other specific tracking needs
- Ensuring that the reporting systems are kept up to date
- Organizing meetings with local Investigator, webcasts, TCs or other meeting formats
START: ASAP
DURATION: 12MM+
LOCATION: Zug, Switzerland
REF.NR.: BH12661
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, Sonstiges