Medical devices
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- 68300 Saint Louis
- Weltweit
- pt | de | fr
- 10.02.2020
Kurzvorstellung
Study coordinator for medical devices studies in Switzerland
Strong inter-personal communication skills are at the heart of my role as I work on a daily basis contact with pharma industrie and investigators.
Strong inter-personal communication skills are at the heart of my role as I work on a daily basis contact with pharma industrie and investigators.
Qualifikationen
Projekt‐ & Berufserfahrung
Study Coordinator (Festanstellung)
Universitätsspital Basel, Basel
4/2014
–
offen
(10 Jahre, 8 Monate)
Tätigkeitszeitraum
4/2014 – offen
TätigkeitsbeschreibungStrong inter-personal communication skills are at the heart of my role as I work on a daily basis with pharma industries and investigators. I will regularly lead technical discussions with the industrie / physicians / patients and will be able to interpret regulatory requirements, pose relevant technical questions and clearly communicate areas of non-conformity.
Eingesetzte QualifikationenForschung & Entwicklung
Ausbildung
DAS in Clinical Trial Practice and Management
DAS in Clinical Trial Practice and Management
2018
Basel Switzerland
Basel Switzerland
Weitere Kenntnisse
A broad technical understanding of Active Implantable Medical Devices.
An understanding of companies operating in these spaces and current industry trends.
Hands-on experience of testing in the AIMD industry, or clinical application of active implantable devices.
An appreciation of risks related to implanted materials.
An appreciation of risks related to use of software in critical applications.
An understanding of Risk Management and FMEA for active implantable devices.
Knowledge of Medical Device regulations and QMS systems for medical devices.
Interpretation and applications of International and National standards for the design, manufacture and regulation of medical devices.
Conceptual and analytical thinking, efficiency and results orientation.
Ability to work independently with minimal supervision; self-motivated.
Being a team player good at relationship building internally and externally.
An understanding of companies operating in these spaces and current industry trends.
Hands-on experience of testing in the AIMD industry, or clinical application of active implantable devices.
An appreciation of risks related to implanted materials.
An appreciation of risks related to use of software in critical applications.
An understanding of Risk Management and FMEA for active implantable devices.
Knowledge of Medical Device regulations and QMS systems for medical devices.
Interpretation and applications of International and National standards for the design, manufacture and regulation of medical devices.
Conceptual and analytical thinking, efficiency and results orientation.
Ability to work independently with minimal supervision; self-motivated.
Being a team player good at relationship building internally and externally.
Persönliche Daten
Sprache
- Deutsch (Fließend)
- Portugiesisch (Muttersprache)
- Französisch (Fließend)
- Englisch (Fließend)
Reisebereitschaft
Weltweit
Arbeitserlaubnis
- Europäische Union
- Schweiz
Profilaufrufe
1320
Alter
44
Berufserfahrung
14 Jahre und 3 Monate
(seit 08/2010)
Projektleitung
4 Jahre
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