Immatics Biotechnologies GmbH
(Senior) Clinical Statistical Programmer – SAS*(m/w/x)
Full-timeWith HomeofficeExperienced
Tübingen, München
New Job?Nejo!
The AI Job Search Engine
PS
PSI CROClinical Data Scientist(m/w/x)
München
Full-timeWith Home OfficeExperienced
AI/ML
Data Science
Description
As a Clinical Data Scientist, you will engage in setting up risk-based monitoring systems and developing analytical tools, while also visualizing clinical trial data and ensuring compliance with regulatory standards. This role involves transforming complex datasets and collaborating with cross-functional teams to deliver effective data-driven solutions.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Degree in Data Science, Mathematics, Statistics, Computer Science, or equivalent
- •Minimum 4 years of R and R Shiny programming experience in Clinical/Pharmaceutical domain
- •Experience in custom R Shiny application development using structured frameworks such as golem
- •Proven proficiency in R visualization and reporting packages, such as shiny, R Markdown
- •Solid data wrangling skills in R using packages such as dplyr, lubridate
- •Experience working with diverse data sources, including relational databases, Excel files, and SAS datasets
- •Practical experience in developing and maintaining R packages
- •Familiarity with version control workflows, including Git
- •Full professional proficiency in English
- •Strong analytical and logical thinking
- •Communication and collaboration skills
- •Experience in data engineering including relational databases, data warehousing, data modeling
- •Experience in R Shiny frontend customization using CSS and JavaScript
- •Object-oriented programming for R R6
- •Azure Services: DevOps, Synapse
- •Atlassian Products: Jira, Confluence
- •Experience with CluePoints RBM system
- •Knowledge of statistical methods and techniques for analyzing data
- •Experience using Machine Learning techniques and products testing and validation
Education
Bachelor's degree
Work Experience
4 years
Tasks
- •Set up and maintain risk-based monitoring systems
- •Develop and program Key Risk Indicators and Quality Tolerance Limits
- •Create Tables, Figures, and Listings for trial oversight
- •Program and maintain interactive dashboards using R and R Shiny
- •Visualize clinical trial data for medical review and risk assessment
- •Manage and transform complex datasets from multiple sources
- •Integrate datasets into the PSI data platform for analysis
- •Advise on new tools and methodologies for clinical trial analytics
- •Ensure compliance with regulatory standards and quality expectations
- •Collaborate with teams to identify study-level challenges
Tools & Technologies
RR ShinydplyrlubridateshinyR MarkdownGitAzure ServicesJiraConfluence
Languages
English – Business Fluent
Benefits
Flexible Working
- •Flexible working hours
More Vacation Days
- •Additional days off
Other Benefits
- •Life insurance
Healthcare & Fitness
- •Medical insurance
Corporate Discounts
- •Sports card
Free or Subsidized Food
- •Lunch card
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of PSI CRO and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Not a perfect match?
- Machine Learning Reply
Data Scientist(m/w/x)
Full-timeWith HomeofficeExperiencedMünchen - Machine Learning Reply
Senior Data Scientist(m/w/x)
Full-timeWith HomeofficeManagementMünchen - PSI CRO
Principal Lead Data Manager(m/w/x)
Full-timeWith HomeofficeSeniorMünchen - Alira Health GmbH
Medical Monitor(m/w/x)
Full-timeWith HomeofficeExperiencedMünchen
PS
PSI CROClinical Data Scientist(m/w/x)
München
Full-timeWith Home OfficeExperienced
AI/ML
Data Science
New Job?Nejo!
The AI Job Search Engine
Description
As a Clinical Data Scientist, you will engage in setting up risk-based monitoring systems and developing analytical tools, while also visualizing clinical trial data and ensuring compliance with regulatory standards. This role involves transforming complex datasets and collaborating with cross-functional teams to deliver effective data-driven solutions.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Degree in Data Science, Mathematics, Statistics, Computer Science, or equivalent
- •Minimum 4 years of R and R Shiny programming experience in Clinical/Pharmaceutical domain
- •Experience in custom R Shiny application development using structured frameworks such as golem
- •Proven proficiency in R visualization and reporting packages, such as shiny, R Markdown
- •Solid data wrangling skills in R using packages such as dplyr, lubridate
- •Experience working with diverse data sources, including relational databases, Excel files, and SAS datasets
- •Practical experience in developing and maintaining R packages
- •Familiarity with version control workflows, including Git
- •Full professional proficiency in English
- •Strong analytical and logical thinking
- •Communication and collaboration skills
- •Experience in data engineering including relational databases, data warehousing, data modeling
- •Experience in R Shiny frontend customization using CSS and JavaScript
- •Object-oriented programming for R R6
- •Azure Services: DevOps, Synapse
- •Atlassian Products: Jira, Confluence
- •Experience with CluePoints RBM system
- •Knowledge of statistical methods and techniques for analyzing data
- •Experience using Machine Learning techniques and products testing and validation
Education
Bachelor's degree
Work Experience
4 years
Tasks
- •Set up and maintain risk-based monitoring systems
- •Develop and program Key Risk Indicators and Quality Tolerance Limits
- •Create Tables, Figures, and Listings for trial oversight
- •Program and maintain interactive dashboards using R and R Shiny
- •Visualize clinical trial data for medical review and risk assessment
- •Manage and transform complex datasets from multiple sources
- •Integrate datasets into the PSI data platform for analysis
- •Advise on new tools and methodologies for clinical trial analytics
- •Ensure compliance with regulatory standards and quality expectations
- •Collaborate with teams to identify study-level challenges
Tools & Technologies
RR ShinydplyrlubridateshinyR MarkdownGitAzure ServicesJiraConfluence
Languages
English – Business Fluent
Benefits
Flexible Working
- •Flexible working hours
More Vacation Days
- •Additional days off
Other Benefits
- •Life insurance
Healthcare & Fitness
- •Medical insurance
Corporate Discounts
- •Sports card
Free or Subsidized Food
- •Lunch card
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of PSI CRO and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
PSI CRO
Industry
Pharmaceuticals
Description
The company is a leading Contract Research Organization with almost 30 years on the market, offering a perfect balance between stability and innovation.
Not a perfect match?
- Immatics Biotechnologies GmbH
(Senior) Clinical Statistical Programmer – SAS*(m/w/x)
Full-timeWith HomeofficeExperiencedTübingen, München - Machine Learning Reply
Data Scientist(m/w/x)
Full-timeWith HomeofficeExperiencedMünchen - Machine Learning Reply
Senior Data Scientist(m/w/x)
Full-timeWith HomeofficeManagementMünchen - PSI CRO
Principal Lead Data Manager(m/w/x)
Full-timeWith HomeofficeSeniorMünchen - Alira Health GmbH
Medical Monitor(m/w/x)
Full-timeWith HomeofficeExperiencedMünchen