Digital Biomarkers Computer Systems Validation Expert (f/m/d)

Basel  ‐ Vor Ort
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Beschreibung

Digital Biomarkers Computer Systems Validation Expert (f/m/d) - CSV /SCRUM/ SW Development / Cloud / English

Project:
For our customer a big pharmaceutical company in Basel we are looking for a highly qualified Digital Biomarkers Computer Systems Validation Expert.

Background:

The Client's Research and Early Development Informatics team is the bridge between digital technology and science. They help drive medical innovation and are integral to the realization of truly Personalized Healthcare and the development of innovative treatments for our patients. Their organization is growing, and they are shaping the digitization of Pharma R&D. They will continue to be the best scientific Informatics partner in the pharmaceutical industry, and need innovative, dedicated people from a wide variety of backgrounds as we realize our vision. Digital tools, such as smartphones or wearables, can now continually measure and collect vital health information - or "digital biomarkers" - from patients. Digital biomarkers are changing how future medicines will be developed and could lead to more personalized use of new medications that will transform the lives of patients. Advances in wearable devices, such as phones, watches, textiles or delivery devices, which track a patient's vital signs and monitor for symptoms all have the potential to vastly accelerate clinical development. The Digital Biomarker program's objective is to develop digital biomarkers. Here we are looking for a Computer Systems Validation Expert. We are looking for a CSV Expert to take on the Validation Lead role in a new back-end validation project. This person will be responsible for the CSV validation of systems including data analysis algorithms, working in close collaboration with technical team members responsible for software development and data analysts, responsible for algorithm development. The client is open from professionals, up to seniors and just transfer responsibilities regarding the CVs/ experiences we receive.
Tasks & Responsibilities :
  • Validation lead position for clinical data processing platform
  • Creating validation documentation
  • Foundation of strategy
  • Supporting data analysis team
  • Responsible for validation, lead other validation resources
  • Also includes project management components
Start
11/2022
Dauer
18++
(Verlängerung möglich)
Von
ITech Consult AG
Eingestellt
26.09.2022
Projekt-ID:
2468178
Vertragsart
Freiberuflich
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