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Projektbeschreibung
* Anonymisation of patient level data from clinical trials (typically SAS datasets) in close, cross functional collaboration e.g. with trial/project teams (incl. Data Management, Statistics, Statistical Programming), Data Sharing Coordinator, Data Protection Officer, Legal
* Development and maintenance of methods and tools (e.g. SAS macros and template programs) for the anonymisation of clinical trial data for the purpose of sharing with internal requestors and external researchers (e.g. via ClinicalStudyDataRequest.com) in accordance with national, EU and other applicable data protection regulations and internal procedures on the protection of commercially confidential information and intellectual property
* Subject matter expert for other functions to support customized sharing activities
VORAUSSETZUNGEN:
* Bachelor-s or Master-s degree with IT/IS, math/statistics or comparable focus
* At least two to three years of experience within the pharmaceutical industry, CROs or academic sites with international exposure
* Excellent working knowledge of all aspects of the SAS programming language, incl. macro programming with focus on collection, processing or analysis of clinical trial data
* Knowledge of anonymisation concepts and methods (key words: suppression, generalisation, randomisation; k-anonymity, risk of re-identification) and tools (e.g. ARX De-Identifier), ideally experience in the anonymisation of clinical trial data
* Strong communication and negotiation skills
* Excellent in English
* Development and maintenance of methods and tools (e.g. SAS macros and template programs) for the anonymisation of clinical trial data for the purpose of sharing with internal requestors and external researchers (e.g. via ClinicalStudyDataRequest.com) in accordance with national, EU and other applicable data protection regulations and internal procedures on the protection of commercially confidential information and intellectual property
* Subject matter expert for other functions to support customized sharing activities
VORAUSSETZUNGEN:
* Bachelor-s or Master-s degree with IT/IS, math/statistics or comparable focus
* At least two to three years of experience within the pharmaceutical industry, CROs or academic sites with international exposure
* Excellent working knowledge of all aspects of the SAS programming language, incl. macro programming with focus on collection, processing or analysis of clinical trial data
* Knowledge of anonymisation concepts and methods (key words: suppression, generalisation, randomisation; k-anonymity, risk of re-identification) and tools (e.g. ARX De-Identifier), ideally experience in the anonymisation of clinical trial data
* Strong communication and negotiation skills
* Excellent in English
Projektdetails
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Einsatzort:
Großraum Ulm, Deutschland
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Projektbeginn:
asap
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Projektdauer:
48 Woche(n)
- Vertragsart:
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Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
Sonstiges