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Safety Manager
Eingestellt von RM IT Professional Resources AG
Gesuchte Skills: Client, Support
Projektbeschreibung
Safety Manager wanted for our Zug based client in the pharmaceutical sector.
YOUR EXPERIENCE/SKILLS:
- Good knowledge of pharmacological and medical terminology
- Know-how of national and international regulations for pharmacovigilance
- Professionalism with timeliness and quality assurance
- Working experience in a global team and country specific departments
- Languages: fluent English and German both written and spoken
YOUR TASKS:
- Managing data safety and flow of information of all adverse event reports for all products, such as clinical trials and non interventional studies
- Coordinating reporting, submission and distribution of safety information, like DSUR, SAE, Biannual SUSAR Listing, IN/SUSAR, to Local Health Authorities and clinical operations
- Participating in collaboration with either local or global Patient Safety associations and evaluating safety data
- Supervising pharmacovigilance instructions and reporting updates to global Patient Safety organisations
- Creating training materials for pharmacovigilance and training of Country Organization associates on relevant Patient Safety procedures
START: ASAP
DURATION: 09MM+
LOCATION: Zug, Switzerland
REF.NR.: BH11544
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:
- Good knowledge of pharmacological and medical terminology
- Know-how of national and international regulations for pharmacovigilance
- Professionalism with timeliness and quality assurance
- Working experience in a global team and country specific departments
- Languages: fluent English and German both written and spoken
YOUR TASKS:
- Managing data safety and flow of information of all adverse event reports for all products, such as clinical trials and non interventional studies
- Coordinating reporting, submission and distribution of safety information, like DSUR, SAE, Biannual SUSAR Listing, IN/SUSAR, to Local Health Authorities and clinical operations
- Participating in collaboration with either local or global Patient Safety associations and evaluating safety data
- Supervising pharmacovigilance instructions and reporting updates to global Patient Safety organisations
- Creating training materials for pharmacovigilance and training of Country Organization associates on relevant Patient Safety procedures
START: ASAP
DURATION: 09MM+
LOCATION: Zug, Switzerland
REF.NR.: BH11544
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