General information: Start date: ASAP Duration: 12 months (extension possible) Workload: 100% Work location: Basel On behalf of our client we are looking for an experienced Clinical Study Data Engineer to ensure the successful implementation of a Clinical Platform application, which streamlines clinical study management in early phase trials. To succeed in this role you will develop a strong understanding of the data flow from collection to analysis and filing to user access. Main tasks:
Organisation, data flow, and integration of clinical and medical data of various types, such as binary images, image masks, tabular bioassay and tabular clinical data
Leading activities around data flows and interfaces to retrieve clinical image data and image annotations, and establishing data standards with external partners
Leading regular data integration efforts with external and internal partners, standardizing interfaces and providing feedback on relevant specifications
Data wrangling of heterogeneous, multimodal and longitudinal data to perform QC and discover new insights
Developing robust and fit-for-purpose solutions for data management, governance, provisioning, QC, and visualisation using databases, file systems, and cloud platforms
Documenting datasets and dataset access services and maintaining dataset specifications
Establishing links between existing infrastructure and semantic storage and retrieval capabilities
Qualification and Experience:
M.Sc in Computer Science, Biology or similar discipline
Very good practical IT skills and mastering of standard technologies (Web services, HTTP, UNIX, shell programming)
Proven experience with data warehousing, data ingestion, and data profiling
Proficiency with relational database queries (SQL), pivoting data, and working with clinical data standards(e.g. SDTM format)
Ability to work out and report on data summaries of clinical datasets and dataset samples
Proficient in Python and/or R, and git
Clinical imaging experience (preferably Ophthalmology, Neurology or similar)
Proficiency with standard medical image formats (e.g. DICOM, TIFF, MHD)
Proficiency with proprietary formats is a plus
Comfortable working with other teams, scientific computing and data architects, to offer robust and fit-for-purpose solutions
Communication skills for presenting results and ensuring alignment with stakeholders and business partners. Mastering of business intelligence software (e.g. Spotfire)
Strong team player, flexible and with a high degree of self-organization, proactive and able to work in matrix environment
Fluent in English
21/02/2020
Full time
General information: Start date: ASAP Duration: 12 months (extension possible) Workload: 100% Work location: Basel On behalf of our client we are looking for an experienced Clinical Study Data Engineer to ensure the successful implementation of a Clinical Platform application, which streamlines clinical study management in early phase trials. To succeed in this role you will develop a strong understanding of the data flow from collection to analysis and filing to user access. Main tasks:
Organisation, data flow, and integration of clinical and medical data of various types, such as binary images, image masks, tabular bioassay and tabular clinical data
Leading activities around data flows and interfaces to retrieve clinical image data and image annotations, and establishing data standards with external partners
Leading regular data integration efforts with external and internal partners, standardizing interfaces and providing feedback on relevant specifications
Data wrangling of heterogeneous, multimodal and longitudinal data to perform QC and discover new insights
Developing robust and fit-for-purpose solutions for data management, governance, provisioning, QC, and visualisation using databases, file systems, and cloud platforms
Documenting datasets and dataset access services and maintaining dataset specifications
Establishing links between existing infrastructure and semantic storage and retrieval capabilities
Qualification and Experience:
M.Sc in Computer Science, Biology or similar discipline
Very good practical IT skills and mastering of standard technologies (Web services, HTTP, UNIX, shell programming)
Proven experience with data warehousing, data ingestion, and data profiling
Proficiency with relational database queries (SQL), pivoting data, and working with clinical data standards(e.g. SDTM format)
Ability to work out and report on data summaries of clinical datasets and dataset samples
Proficient in Python and/or R, and git
Clinical imaging experience (preferably Ophthalmology, Neurology or similar)
Proficiency with standard medical image formats (e.g. DICOM, TIFF, MHD)
Proficiency with proprietary formats is a plus
Comfortable working with other teams, scientific computing and data architects, to offer robust and fit-for-purpose solutions
Communication skills for presenting results and ensuring alignment with stakeholders and business partners. Mastering of business intelligence software (e.g. Spotfire)
Strong team player, flexible and with a high degree of self-organization, proactive and able to work in matrix environment
Fluent in English
An excellent multinational healthcare company is seeking a skilled Study Data Manager, to be based in their office in the desirable area of Basel. The organisation is known internationally for their work in pharmaceuticals and diagnostics and their focus on scientific advancement. This is a chance to join a top healthcare organisation who provide an innovative range of diagnostic solutions and medicines.
Job Responsibilities:
Working within a team of experts in data life-cycle management who acquire and curate data for use in exploratory research, clinical development and evidence generation.
Collaborating with peers within the function and across the organisation to identify, design and execute fit for purpose data management solutions, adhering to F.A.I.R. (Findable, Accessible, Interoperable, Reusable) principles.
Ensuring the timely completion of data management deliverables and partner with Functional Service Providers (FSPs) and vendors, overseeing and providing technical expertise in the delivery of high-quality data.
Contributing to functional, cross functional, enterprise-wide or external initiatives that shape our technical landscape, business and healthcare environments.
In charge of making sure the data coming in is proper, compliant and delivered on time, including includes data review & cleaning.
Overseeing both internal and external stakeholders (supplier in India amongst other).
Developing risk management strategies and proactively manage timelines to ensure successful oversight and delivery of studies, projects and coding responsibilities, including the implementation and adoption of new technologies.
Proactively engage with stakeholders across the business to understand their needs and influence their understanding of decisions made in our function. Inform stakeholders of status of key deliverables and act on changing milestones.
Partnering with relevant functions for external data vendor selection and management. Oversee development of data transfer agreements with vendors ensuring use of standards, fit-for-purpose data models and transfer intervals.
Acting as experts for data collection, advising teams and stakeholders on best practices and proposing innovative solutions.
Ensuring a high quality of data and compliance with applicable pharma industry regulations and standards.
Staying current with and adopt emergent data collection, data management, visualisation and provision tools and applications to ensure fit-for-purpose and impactful approaches. Deliver on solutions as needed.
Using data surveillance tools and strategies to provide aggregate level reviews designed to identify patterns or anomalies in our data to ensure high quality results.
Organisation and integration of data collected from various sources. Maintain value of data through application of FAIR (Findable, Accessible, Interoperable, Reusable) principles.
Partnering with stakeholders to understand their data insight needs and offer Data Management solutions. Demonstrate a strong understanding of the data flow from collection through to analysis and filing.
Collaborating and contributing to functional/cross-functional initiatives or goals to promote new ways of working, including emerging technologies. Enable broader and more effective use of data to support the business.
Offering guidance and advice to peers within the function, to key stakeholders and to FSPs, CRO and collaborative groups on technical solutions to ensure high quality data collection and delivery.
Skills and Requirements:
2 years of experience with Data Collection system (e.g. eCRF and others) in pharma
2 years of experience with data management (e.g. data cleaning, data review)
1 year of experience in Clinical Development (early phases preferred)
Project Management skills (track record of on time delivery for multiple requests and stakeholder management).
Knowledge of CDISC data standards.
Knowledge of ICH-GCP and working in regulated environments
Experience in a global matrix environment is a plus
Good understanding of molecule and disease area strategies, healthcare environments, as well as strong scientific and technical expertise is a plus
Strong strategic, collaboration and communication skills, as well as an entrepreneurial mindset, to evolve the way we collect and deliver data and to develop and deliver medicines for our patients.
Experience of Data Collection System in Clinical Development (eCRF etc) and able to translate a protocol into Case Report Forms.
Project management skills are highly appreciated to be able to manage multiple stakeholders, deadlines and work streams.
Clinical Development in pharma experience is necessary
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please contact Tom Magenis at 0203 854 1050 or upload your CV on our website - www.proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
#LI-TM1
#Biometrics
21/02/2020
Full time
An excellent multinational healthcare company is seeking a skilled Study Data Manager, to be based in their office in the desirable area of Basel. The organisation is known internationally for their work in pharmaceuticals and diagnostics and their focus on scientific advancement. This is a chance to join a top healthcare organisation who provide an innovative range of diagnostic solutions and medicines.
Job Responsibilities:
Working within a team of experts in data life-cycle management who acquire and curate data for use in exploratory research, clinical development and evidence generation.
Collaborating with peers within the function and across the organisation to identify, design and execute fit for purpose data management solutions, adhering to F.A.I.R. (Findable, Accessible, Interoperable, Reusable) principles.
Ensuring the timely completion of data management deliverables and partner with Functional Service Providers (FSPs) and vendors, overseeing and providing technical expertise in the delivery of high-quality data.
Contributing to functional, cross functional, enterprise-wide or external initiatives that shape our technical landscape, business and healthcare environments.
In charge of making sure the data coming in is proper, compliant and delivered on time, including includes data review & cleaning.
Overseeing both internal and external stakeholders (supplier in India amongst other).
Developing risk management strategies and proactively manage timelines to ensure successful oversight and delivery of studies, projects and coding responsibilities, including the implementation and adoption of new technologies.
Proactively engage with stakeholders across the business to understand their needs and influence their understanding of decisions made in our function. Inform stakeholders of status of key deliverables and act on changing milestones.
Partnering with relevant functions for external data vendor selection and management. Oversee development of data transfer agreements with vendors ensuring use of standards, fit-for-purpose data models and transfer intervals.
Acting as experts for data collection, advising teams and stakeholders on best practices and proposing innovative solutions.
Ensuring a high quality of data and compliance with applicable pharma industry regulations and standards.
Staying current with and adopt emergent data collection, data management, visualisation and provision tools and applications to ensure fit-for-purpose and impactful approaches. Deliver on solutions as needed.
Using data surveillance tools and strategies to provide aggregate level reviews designed to identify patterns or anomalies in our data to ensure high quality results.
Organisation and integration of data collected from various sources. Maintain value of data through application of FAIR (Findable, Accessible, Interoperable, Reusable) principles.
Partnering with stakeholders to understand their data insight needs and offer Data Management solutions. Demonstrate a strong understanding of the data flow from collection through to analysis and filing.
Collaborating and contributing to functional/cross-functional initiatives or goals to promote new ways of working, including emerging technologies. Enable broader and more effective use of data to support the business.
Offering guidance and advice to peers within the function, to key stakeholders and to FSPs, CRO and collaborative groups on technical solutions to ensure high quality data collection and delivery.
Skills and Requirements:
2 years of experience with Data Collection system (e.g. eCRF and others) in pharma
2 years of experience with data management (e.g. data cleaning, data review)
1 year of experience in Clinical Development (early phases preferred)
Project Management skills (track record of on time delivery for multiple requests and stakeholder management).
Knowledge of CDISC data standards.
Knowledge of ICH-GCP and working in regulated environments
Experience in a global matrix environment is a plus
Good understanding of molecule and disease area strategies, healthcare environments, as well as strong scientific and technical expertise is a plus
Strong strategic, collaboration and communication skills, as well as an entrepreneurial mindset, to evolve the way we collect and deliver data and to develop and deliver medicines for our patients.
Experience of Data Collection System in Clinical Development (eCRF etc) and able to translate a protocol into Case Report Forms.
Project management skills are highly appreciated to be able to manage multiple stakeholders, deadlines and work streams.
Clinical Development in pharma experience is necessary
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please contact Tom Magenis at 0203 854 1050 or upload your CV on our website - www.proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
#LI-TM1
#Biometrics
General information: Start date: ASAP Duration: 12 months (extension possible) Workload: 100% Work location: Basel On behalf of our client we are looking for an experienced Clinical Study Data Engineer to ensure the successful implementation of a Clinical Platform application, which streamlines clinical study management in early phase trials. To succeed in this role you will develop a strong understanding of the data flow from collection to analysis and filing to user access. Main tasks:
Organisation, data flow, and integration of clinical and medical data of various types, such as binary images, image masks, tabular bioassay and tabular clinical data
Leading activities around data flows and interfaces to retrieve clinical image data and image annotations, and establishing data standards with external partners
Leading regular data integration efforts with external and internal partners, standardizing interfaces and providing feedback on relevant specifications
Data wrangling of heterogeneous, multimodal and longitudinal data to perform QC and discover new insights
Developing robust and fit-for-purpose solutions for data management, governance, provisioning, QC, and visualisation using databases, file systems, and cloud platforms
Documenting datasets and dataset access services and maintaining dataset specifications
Establishing links between existing infrastructure and semantic storage and retrieval capabilities
Qualification and Experience:
M.Sc in Computer Science, Biology or similar discipline
Very good practical IT skills and mastering of standard technologies (Web services, HTTP, UNIX, shell programming)
Proven experience with data warehousing, data ingestion, and data profiling
Proficiency with relational database queries (SQL), pivoting data, and working with clinical data standards(e.g. SDTM format)
Ability to work out and report on data summaries of clinical datasets and dataset samples
Proficient in Python and/or R, and git
Clinical imaging experience (preferably Ophthalmology, Neurology or similar)
Proficiency with standard medical image formats (e.g. DICOM, TIFF, MHD)
Proficiency with proprietary formats is a plus
Comfortable working with other teams, scientific computing and data architects, to offer robust and fit-for-purpose solutions
Communication skills for presenting results and ensuring alignment with stakeholders and business partners. Mastering of business intelligence software (e.g. Spotfire)
Strong team player, flexible and with a high degree of self-organization, proactive and able to work in matrix environment
Fluent in English
17/02/2020
Full time
General information: Start date: ASAP Duration: 12 months (extension possible) Workload: 100% Work location: Basel On behalf of our client we are looking for an experienced Clinical Study Data Engineer to ensure the successful implementation of a Clinical Platform application, which streamlines clinical study management in early phase trials. To succeed in this role you will develop a strong understanding of the data flow from collection to analysis and filing to user access. Main tasks:
Organisation, data flow, and integration of clinical and medical data of various types, such as binary images, image masks, tabular bioassay and tabular clinical data
Leading activities around data flows and interfaces to retrieve clinical image data and image annotations, and establishing data standards with external partners
Leading regular data integration efforts with external and internal partners, standardizing interfaces and providing feedback on relevant specifications
Data wrangling of heterogeneous, multimodal and longitudinal data to perform QC and discover new insights
Developing robust and fit-for-purpose solutions for data management, governance, provisioning, QC, and visualisation using databases, file systems, and cloud platforms
Documenting datasets and dataset access services and maintaining dataset specifications
Establishing links between existing infrastructure and semantic storage and retrieval capabilities
Qualification and Experience:
M.Sc in Computer Science, Biology or similar discipline
Very good practical IT skills and mastering of standard technologies (Web services, HTTP, UNIX, shell programming)
Proven experience with data warehousing, data ingestion, and data profiling
Proficiency with relational database queries (SQL), pivoting data, and working with clinical data standards(e.g. SDTM format)
Ability to work out and report on data summaries of clinical datasets and dataset samples
Proficient in Python and/or R, and git
Clinical imaging experience (preferably Ophthalmology, Neurology or similar)
Proficiency with standard medical image formats (e.g. DICOM, TIFF, MHD)
Proficiency with proprietary formats is a plus
Comfortable working with other teams, scientific computing and data architects, to offer robust and fit-for-purpose solutions
Communication skills for presenting results and ensuring alignment with stakeholders and business partners. Mastering of business intelligence software (e.g. Spotfire)
Strong team player, flexible and with a high degree of self-organization, proactive and able to work in matrix environment
Fluent in English
We develop, manufacture and supply dental implants, clear aligners, instruments, CADCAM prosthetics and biomaterials for use in esthetic dentistry, tooth replacement and restoration solutions or to prevent tooth loss. We empower our employees to perform and make an impact, to question the status quo, to drive change, to stay ahead of the competition. From the first Dental Implant in 1974 to the latest Digital Solution – we do things differently than others We deliver innovation based on evidence. This is part of our employer culture as well as an exceptional team spirit that truly encourages diversity and a powerful “can-do” attitude.
#WeChangeDentistry every day. Be part of it.
Job Description
In the role of SAP BI Solution Architect (m/f/x) (100%) you are part of a small internal development team and you will work closely with our internal business partners from Corporate Accounting, Operational Excellence, Sales Excellence, Human Resources, Procurement and Logistics. The position is based in Basel, Switzerland and reports to the Head of Business Intelligence.
Your main tasks and responsibility will be to
Work closely with the internal customers to understand their needs and provide decision making support
Define and implement technical solutions for diverse business partners
Facilitate technical designs with implementation partners
Play an active role in the application maintenance support
Qualifications
Bachelor’s degree in Computer Science, Business Information Systems or a related technical field
5+ years’ experience in designing and building SAP BI based reporting solutions, preferably with BW 7.50 on HANA or BW/4HANA
Experience with SAP BI IP Integrated Planning, Lumira (Design Studio), SAP Analytics Cloud would be beneficial
Good programming skills in ABAP required. Experience with HANA optimized SQL or VBA Macros is a plus
Basic process knowledge of SAP ERP or SAP CRM would be beneficial
Fluent English and German language skills
Experience in project tracking, deviation monitoring, and steering
Experienced working in interdisciplinary teams on multiple projects in parallel within a culturally diverse, high paced organization
Additional Information
What can you expect from us?
An agile and ambitious environment: We are #ChangeMakers.
Open, friendly colleagues who #collaborate and #support each other: We are # Players+Learners .
The #freedom to #create and #engage : You can leave your #FootprintInDentistry .
An employer who invests in our #inspiring corporate #culture .
The #opportunity to develop yourself as a person and in your #career . We #grow.
#Attractive workplaces at great locations - We are a #GlobalPlayer .
A good salary and many other cool #benefits (depending on location).
To work for the No. 1 in #Dentistry and one of the leading #MedTech companies.
and many other things more!
i-p-r
What do people say about us as an employer? See reviews on Indeed - Glassdoor - Kununu (German)
Stay tuned and connect with us! @straumannjobs at LinkedIn - Xing - Twitter - Instagram - Pinterest - Quora
Please understand that we do not need external support by recruiting agencies and consultants to fill this vacancy. Thank you for respecting this.
17/02/2020
Full time
We develop, manufacture and supply dental implants, clear aligners, instruments, CADCAM prosthetics and biomaterials for use in esthetic dentistry, tooth replacement and restoration solutions or to prevent tooth loss. We empower our employees to perform and make an impact, to question the status quo, to drive change, to stay ahead of the competition. From the first Dental Implant in 1974 to the latest Digital Solution – we do things differently than others We deliver innovation based on evidence. This is part of our employer culture as well as an exceptional team spirit that truly encourages diversity and a powerful “can-do” attitude.
#WeChangeDentistry every day. Be part of it.
Job Description
In the role of SAP BI Solution Architect (m/f/x) (100%) you are part of a small internal development team and you will work closely with our internal business partners from Corporate Accounting, Operational Excellence, Sales Excellence, Human Resources, Procurement and Logistics. The position is based in Basel, Switzerland and reports to the Head of Business Intelligence.
Your main tasks and responsibility will be to
Work closely with the internal customers to understand their needs and provide decision making support
Define and implement technical solutions for diverse business partners
Facilitate technical designs with implementation partners
Play an active role in the application maintenance support
Qualifications
Bachelor’s degree in Computer Science, Business Information Systems or a related technical field
5+ years’ experience in designing and building SAP BI based reporting solutions, preferably with BW 7.50 on HANA or BW/4HANA
Experience with SAP BI IP Integrated Planning, Lumira (Design Studio), SAP Analytics Cloud would be beneficial
Good programming skills in ABAP required. Experience with HANA optimized SQL or VBA Macros is a plus
Basic process knowledge of SAP ERP or SAP CRM would be beneficial
Fluent English and German language skills
Experience in project tracking, deviation monitoring, and steering
Experienced working in interdisciplinary teams on multiple projects in parallel within a culturally diverse, high paced organization
Additional Information
What can you expect from us?
An agile and ambitious environment: We are #ChangeMakers.
Open, friendly colleagues who #collaborate and #support each other: We are # Players+Learners .
The #freedom to #create and #engage : You can leave your #FootprintInDentistry .
An employer who invests in our #inspiring corporate #culture .
The #opportunity to develop yourself as a person and in your #career . We #grow.
#Attractive workplaces at great locations - We are a #GlobalPlayer .
A good salary and many other cool #benefits (depending on location).
To work for the No. 1 in #Dentistry and one of the leading #MedTech companies.
and many other things more!
i-p-r
What do people say about us as an employer? See reviews on Indeed - Glassdoor - Kununu (German)
Stay tuned and connect with us! @straumannjobs at LinkedIn - Xing - Twitter - Instagram - Pinterest - Quora
Please understand that we do not need external support by recruiting agencies and consultants to fill this vacancy. Thank you for respecting this.
Syngenta is a global leader in agriculture; rooted in science and dedicated to bringing plant potential to life. Each of our 28,000 employees in more than 90 countries work together to solve one of humanity’s most pressing challenges: growing more food with fewer resources. Aquatic Risk Modelling Postdoc We invite you to help us shape the future of agriculture. To support this challenge, the Product Safety team is currently seeking an Aquatic Risk Modelling Postdoc in our Basel, Switzerland HQ office. The Aquatic Risk Modelling Postdoc will be a three years engagement where you will develop an indicator system for the environmental risk of crop protection measures on aquatic systems. This indicator will be a globally applicable digital tool and reflect local environmental conditions and agronomic practices In this role you will: Review Scientific literature on environmental risk indicators Develop environmental risk indicator for aquatic systems system Coordinate with environmental fate, ecotoxicology and environmental risk assessment experts Acquire & maintain scientific and technical modelling expertise Deliver and present relevant novel research (incl. scientific publications & conference presentations) Qualifications We are looking for: Critical knowledge and experience A good understanding of environmental fate, ecological & effect modelling along with current knowledge of risk modelling techniques A PhD degree in a relevant area of science Track record relating to one or more of the following areas: environmental fate and ecotoxicology of chemicals, ecological modelling, ecotoxicological effects, environmental risk indicators, Bayesian Network Models, environmental models, agronomy models Experience in developing and applying models Ability to design, build and analyse environmental systems models Ability to analyse and interpret complex data Readiness for occasional international business travels Critical technical, professional and personal capabilities Commitment to achieve objectives individually and within a team Effective communication skills Strong interpersonal skills Ability to skillfully plan, organize and monitor performance to meet deadlines Motivation towards publishing in peer-reviewed literature Creative problem solving skills We Offer The opportunity to contribute to valuable and impactful work for the agriculture of the future A stimulating international environment -> #bringingplantpotentialtolife An open, multicultural and pleasant working environment with state of the art facilities Flat hierarchy and an open culture Please submit an online application in English via the link enclosed. With your up to date CV please include a motivation letter and university degrees. Lieu principal: CHE-Basel-Bâle Emploi: Management des Ressources Humaines
11/02/2020
Full time
Syngenta is a global leader in agriculture; rooted in science and dedicated to bringing plant potential to life. Each of our 28,000 employees in more than 90 countries work together to solve one of humanity’s most pressing challenges: growing more food with fewer resources. Aquatic Risk Modelling Postdoc We invite you to help us shape the future of agriculture. To support this challenge, the Product Safety team is currently seeking an Aquatic Risk Modelling Postdoc in our Basel, Switzerland HQ office. The Aquatic Risk Modelling Postdoc will be a three years engagement where you will develop an indicator system for the environmental risk of crop protection measures on aquatic systems. This indicator will be a globally applicable digital tool and reflect local environmental conditions and agronomic practices In this role you will: Review Scientific literature on environmental risk indicators Develop environmental risk indicator for aquatic systems system Coordinate with environmental fate, ecotoxicology and environmental risk assessment experts Acquire & maintain scientific and technical modelling expertise Deliver and present relevant novel research (incl. scientific publications & conference presentations) Qualifications We are looking for: Critical knowledge and experience A good understanding of environmental fate, ecological & effect modelling along with current knowledge of risk modelling techniques A PhD degree in a relevant area of science Track record relating to one or more of the following areas: environmental fate and ecotoxicology of chemicals, ecological modelling, ecotoxicological effects, environmental risk indicators, Bayesian Network Models, environmental models, agronomy models Experience in developing and applying models Ability to design, build and analyse environmental systems models Ability to analyse and interpret complex data Readiness for occasional international business travels Critical technical, professional and personal capabilities Commitment to achieve objectives individually and within a team Effective communication skills Strong interpersonal skills Ability to skillfully plan, organize and monitor performance to meet deadlines Motivation towards publishing in peer-reviewed literature Creative problem solving skills We Offer The opportunity to contribute to valuable and impactful work for the agriculture of the future A stimulating international environment -> #bringingplantpotentialtolife An open, multicultural and pleasant working environment with state of the art facilities Flat hierarchy and an open culture Please submit an online application in English via the link enclosed. With your up to date CV please include a motivation letter and university degrees. Lieu principal: CHE-Basel-Bâle Emploi: Management des Ressources Humaines
Leitung von datengetriebenen Projekten
Interdisziplinäres Wissen in Mehrwert für die Kunden umwandeln
Generieren von Ideen und gemeinsame Gestaltung von Lösungen mit dem Kunden
Konzeption und Erstellung von intelligenten Interfaces für Business Users
Kontaktpflege zu bestehenden Kunden
Projektakquise
Ihr Profil:
Ausbildung in Informatik, Wirtschaftsinformatik, Statistik Computational Chemistry
Arbeitserfahrung in der Pharmaindustrie von Vorteil
Kenntnisse in Statistik und Programmierung – R, SAS, SGL, SPARQL, Python, D3
Erfahrung in der Beratung von Vorteil
Begeisterung für Daten, Advanced Analytics, Machine Learning
Fliessende Englischkenntnisse
Reisebereitschaft
Hier finden Sie Angaben zu Zusatzleistungen und Karrieremöglichkeiten: Unsere Vorteile.
03/02/2020
Full time
Leitung von datengetriebenen Projekten
Interdisziplinäres Wissen in Mehrwert für die Kunden umwandeln
Generieren von Ideen und gemeinsame Gestaltung von Lösungen mit dem Kunden
Konzeption und Erstellung von intelligenten Interfaces für Business Users
Kontaktpflege zu bestehenden Kunden
Projektakquise
Ihr Profil:
Ausbildung in Informatik, Wirtschaftsinformatik, Statistik Computational Chemistry
Arbeitserfahrung in der Pharmaindustrie von Vorteil
Kenntnisse in Statistik und Programmierung – R, SAS, SGL, SPARQL, Python, D3
Erfahrung in der Beratung von Vorteil
Begeisterung für Daten, Advanced Analytics, Machine Learning
Fliessende Englischkenntnisse
Reisebereitschaft
Hier finden Sie Angaben zu Zusatzleistungen und Karrieremöglichkeiten: Unsere Vorteile.
A permanent contract with the leader in innovation and high-tech engineering consulting
A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D)
In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva
Your role
For our client, a global healthcare company, we are looking for
Programmer, Data Science support
As a programmer in the Modeling&Simulation group, you support scientists by building and deploying modeling and simulation user-friendly applications through digital tools. Your responsibilities include, but are not limited to
Use programming expertise to develop tailor-made software solutions based on various programming languages (e.g. JavaScript, C#, php, python etc.).
Support and be responsible for defined system administration activities on an allocated/defined system or environment.
Support operational requirements of defined areas of the business e.g. troubleshooting and migration to new versions.
Write all required documentation (e.g. user guides, etc.).
Track, troubleshoot and resolve systems related issues.
Applies an write appropriate testing procedures and scripts
Your profile
Minimum requirements
You are proficient in one or more programming language / environment, including HTML, CSS, JavaScript, .NET (C#), SQL, Python, vba macros (MS Office)
Familiar with Frameworks/applications: Svelte, React, Git (gitbucket), VS code
Strong interpersonal communication skills and ability to manage in a dynamic, ever-changing working environment.
Fluent English (oral and written)
Please note, that we only accept applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit for Switzerland.
23/01/2020
Full time
A permanent contract with the leader in innovation and high-tech engineering consulting
A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D)
In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva
Your role
For our client, a global healthcare company, we are looking for
Programmer, Data Science support
As a programmer in the Modeling&Simulation group, you support scientists by building and deploying modeling and simulation user-friendly applications through digital tools. Your responsibilities include, but are not limited to
Use programming expertise to develop tailor-made software solutions based on various programming languages (e.g. JavaScript, C#, php, python etc.).
Support and be responsible for defined system administration activities on an allocated/defined system or environment.
Support operational requirements of defined areas of the business e.g. troubleshooting and migration to new versions.
Write all required documentation (e.g. user guides, etc.).
Track, troubleshoot and resolve systems related issues.
Applies an write appropriate testing procedures and scripts
Your profile
Minimum requirements
You are proficient in one or more programming language / environment, including HTML, CSS, JavaScript, .NET (C#), SQL, Python, vba macros (MS Office)
Familiar with Frameworks/applications: Svelte, React, Git (gitbucket), VS code
Strong interpersonal communication skills and ability to manage in a dynamic, ever-changing working environment.
Fluent English (oral and written)
Please note, that we only accept applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit for Switzerland.
