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Clinical Data Scientist
Eingestellt von Optimus Search
Gesuchte Skills: Design
Projektbeschreibung
Clinical Data Scientist
Basel
12m Contract
600-800CHF per day
Optimus Search are working with a leading biopharmaceutical company to on-board a Clinical Data Scientist for a contract spanning 2018 and beyond.
The role sits within the Biometrics department and focuses on the application of Data Science principals to Clinical Trial Data. This role represents a shift towards a new way of working in the global industry and offers an exciting opportunity rarely seen outside of consultancies.
CORE TASKS
- Lead Clinical Develop Data Management (CDDM) activities for assigned study
- Write all study Data Management documents
- Organise, monitor and track the testing of data entry screens, data cleaning/review tools, and their implementation in the production environment
- Organise, monitor and track data cleaning, data review, query management, and database lock; makes sure processes are driven in collaboration with key Global Clinical Development stakeholders
- Generate study metrics and status reports
- Ensure STDM deliverables are created, validated and provided as per agreed timelines
- Perform and/or coordinate QC
REQUIREMENTS
- Recognised degree in life sciences, mathematics, statistics, informatics or related disciplines
- Proven experience within the Pharmaceutical or Biotech industry within Clinical Research and/or Clinical Data Management with good level of functional expertise in Data Management
- Good knowledge of international clinical research regulations and requirements
- Experience in clinical trial databases and applications, clinical data flow, data review and CRF design
- Ability to lead and coordinate the activity of Data Scientists allocated to his/her study
- Fluent in written and spoken English
If you're interested in knowing more, please contact Robert Marrett on (see below) to set up a call - Thanks!
Basel
12m Contract
600-800CHF per day
Optimus Search are working with a leading biopharmaceutical company to on-board a Clinical Data Scientist for a contract spanning 2018 and beyond.
The role sits within the Biometrics department and focuses on the application of Data Science principals to Clinical Trial Data. This role represents a shift towards a new way of working in the global industry and offers an exciting opportunity rarely seen outside of consultancies.
CORE TASKS
- Lead Clinical Develop Data Management (CDDM) activities for assigned study
- Write all study Data Management documents
- Organise, monitor and track the testing of data entry screens, data cleaning/review tools, and their implementation in the production environment
- Organise, monitor and track data cleaning, data review, query management, and database lock; makes sure processes are driven in collaboration with key Global Clinical Development stakeholders
- Generate study metrics and status reports
- Ensure STDM deliverables are created, validated and provided as per agreed timelines
- Perform and/or coordinate QC
REQUIREMENTS
- Recognised degree in life sciences, mathematics, statistics, informatics or related disciplines
- Proven experience within the Pharmaceutical or Biotech industry within Clinical Research and/or Clinical Data Management with good level of functional expertise in Data Management
- Good knowledge of international clinical research regulations and requirements
- Experience in clinical trial databases and applications, clinical data flow, data review and CRF design
- Ability to lead and coordinate the activity of Data Scientists allocated to his/her study
- Fluent in written and spoken English
If you're interested in knowing more, please contact Robert Marrett on (see below) to set up a call - Thanks!
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design