2 046 Posti di lavoro per Clinical Trials in Italia

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Actual position's title: Clinical Data Scientist

Reporting to the Clinical Data Science Manager, the Clinical Data Scientist is an integral part of our team here at PSI. You will work with clinical trials patient and operational data, develop new data solutions and set up Risk-based Monitoring systems in Process Improvement department.

• Setting up and maintaining risk-based monitoring (RBM) systems and analytical tools in collaboration with Central Monitoring Managers and Medical teams. Developing and programming Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and Tables, Figures, and Listings (TFLs) to enable proactive trial oversight
• Programming and maintaining interactive dashboards and Patient Profiles using R and R Shiny to visualize clinical trial data and support medical review and risk assessment
• Participating in managing and transforming complex datasets from multiple sources and integrating them into the PSI data platform for analysis
• Advising on and contributing to the development of new tools and methodologies for clinical trial analytics and risk-based monitoring
• Ensuring compliance with regulatory standards, quality expectations, and best practices in clinical trial data management
• Collaborating cross-functionally to identify study-level challenges and deliver tailored data-driven solutions

Must have:

• 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, preferably using structured frameworks such as golem, with a solid understanding of modular architecture and functional programming practices.
• Proven proficiency in one or more R visualization and reporting packages, such as shiny, R Markdown.
• Solid data wrangling skills in R, with hands-on experience 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, with a focus on reusability, robustness, and collaborative development.
• Familiarity with version control workflows, including Git and working within a central code repository.
• Full professional proficiency in English
• Strong analytical and logical thinking
• Communication and collaboration skills

Nice to have:

• Experience in data engineering area including one or more of the following: relationship databases, data warehousing, data schemas, data stores, data modeling
• Object-oriented programming for R ~ R6 (R)
• Atlassian Products: Jira, Confluence
• Experience with CluePoints RBM system
• Knowledge of statistical methodsand techniques for analyzing data
• Experienceusing Machine Learning technics andproducts testing and validation

What we offer:

• We value your time so the recruitment process is as quick as 3 meetings
• We'll prepare you to do your job at highest quality level with our extensive onboarding and mentorship program
• You'll have excellent working conditions - spacious and modern office in convenient location, and friendly, supportive team who love to hang out together
• You'll havepermanent work agreement at a stable, privately owned company
• We care about our employees - aside from competitive salary, you'll have good work-life balance with flexible working hours and additional days off, life and medical insurance, sports card, lunch card
• We're constantly growing which meansopportunities for personal and professional growth

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Actual position's title: Clinical Data Scientist

Reporting to the Clinical Data Science Manager, the Clinical Data Scientist is an integral part of our team here at PSI. You will work with clinical trials patient and operational data, develop new data solutions and set up Risk-based Monitoring systems in Process Improvement department. Hybrid work in Milan.

• Setting up and maintaining risk-based monitoring (RBM) systems and analytical tools in collaboration with Central Monitoring Managers and Medical teams. Developing and programming Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and Tables, Figures, and Listings (TFLs) to enable proactive trial oversight
• Programming and maintaining interactive dashboards and Patient Profiles using R and R Shiny to visualize clinical trial data and support medical review and risk assessment
• Participating in managing and transforming complex datasets from multiple sources and integrating them into the PSI data platform for analysis
• Advising on and contributing to the development of new tools and methodologies for clinical trial analytics and risk-based monitoring
• Ensuring compliance with regulatory standards, quality expectations, and best practices in clinical trial data management
• Collaborating cross-functionally to identify study-level challenges and deliver tailored data-driven solutions

• 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, preferably using structured frameworks such as golem, with a solid understanding of modular architecture and functional programming practices.
• Proven proficiency in one or more R visualization and reporting packages, such as shiny, R Markdown.
• Solid data wrangling skills in R, with hands-on experience 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, with a focus on reusability, robustness, and collaborative development.
• Familiarity with version control workflows, including Git and working within a central code repository.
• Full professional proficiency in English
• Strong analytical and logical thinking
• Communication and collaboration skills

• Experience in data engineering area including one or more of the following: relationship databases, data warehousing, data schemas, data stores, data modeling
• Experience in R Shiny frontend customization using CSS and JavaScript for enhanced user interface and interactivity.
• Object-oriented programming for R : R6 (R)
• 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 technics and products testing and validation

• We value your time so the recruitment process is as quick as 3 meetings
• We'll prepare you to do your job at highest quality level with our extensive onboarding and mentorship program
• You'll have excellent working conditions - spacious and modern office in convenient location, and friendly, supportive team who love to hang out together
• You'll have permanent work agreement at a stable, privately owned company
• We care about our employees - aside from competitive salary, you'll have good work-life balance with flexible working hours and additional days off, life and medical insurance, sports card, lunch card
• We're constantly growing which means opportunities for personal and professional growth

Please submit your CV in English.

• Associate

• Full-time

• Analyst

• Pharmaceutical Manufacturing

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Actual position's title: Clinical Data Scientist

Reporting to the Clinical Data Science Manager, the Clinical Data Scientist is an integral part of our team here at PSI. You will work with clinical trials patient and operational data, develop new data solutions and set up Risk-based Monitoring systems in Process Improvement department.

Hybrid work in Milan

• Setting up and maintaining risk-based monitoring (RBM) systems and analytical tools in collaboration with Central Monitoring Managers and Medical teams. Developing and programming Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and Tables, Figures, and Listings (TFLs) to enable proactive trial oversight
• Programming and maintaining interactive dashboards and Patient Profiles using R and R Shiny to visualize clinical trial data and support medical review and risk assessment
• Participating in managing and transforming complex datasets from multiple sources and integrating them into the PSI data platform for analysis
• Advising on and contributing to the development of new tools and methodologies for clinical trial analytics and risk-based monitoring
• Ensuring compliance with regulatory standards, quality expectations, and best practices in clinical trial data management
• Collaborating cross-functionally to identify study-level challenges and deliver tailored data-driven solutions

Must have:

• 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, preferably using structured frameworks such as golem, with a solid understanding of modular architecture and functional programming practices.
• Proven proficiency in one or more R visualization and reporting packages, such as shiny, R Markdown.
• Solid data wrangling skills in R, with hands-on experience 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, with a focus on reusability, robustness, and collaborative development.
• Familiarity with version control workflows, including Git and working within a central code repository.
• Full professional proficiency in English
• Strong analytical and logical thinking
• Communication and collaboration skills

Nice to have:

• Experience in data engineering area including one or more of the following: relationship databases, data warehousing, data schemas, data stores, data modeling
• Experience in R Shiny frontend customization using CSS and JavaScript for enhanced user interface and interactivity.
• Object-oriented programming for R ~ R6 (R)
• Azure Services: DevOps, Synapse
• Atlassian Products: Jira, Confluence
• Experience with CluePoints RBM system
• Knowledge of statistical methodsand techniques for analyzing data
• Experienceusing Machine Learning technics andproducts testing and validation

What we offer:

• We value your time so the recruitment process is as quick as 3 meetings
• We'll prepare you to do your job at highest quality level with our extensive onboarding and mentorship program
• You'll have excellent working conditions - spacious and modern office in convenient location, and friendly, supportive team who love to hang out together
• You'll havepermanent work agreement at a stable, privately owned company
• We care about our employees - aside from competitive salary, you'll have good work-life balance with flexible working hours and additional days off, life and medical insurance, sports card, lunch card
• We're constantly growing which meansopportunities for personal and professional growth

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

Please submit your CV in English

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Actual position's title: Clinical Data Scientist

Reporting to the Clinical Data Science Manager, the Clinical Data Scientist is an integral part of our team here at PSI. You will work with clinical trials patient and operational data, develop new data solutions and set up Risk-based Monitoring systems in Process Improvement department.

Hybrid work in Milan

• Setting up and maintaining risk-based monitoring (RBM) systems and analytical tools in collaboration with Central Monitoring Managers and Medical teams. Developing and programming Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and Tables, Figures, and Listings (TFLs) to enable proactive trial oversight
• Programming and maintaining interactive dashboards and Patient Profiles using R and R Shiny to visualize clinical trial data and support medical review and risk assessment
• Participating in managing and transforming complex datasets from multiple sources and integrating them into the PSI data platform for analysis
• Advising on and contributing to the development of new tools and methodologies for clinical trial analytics and risk-based monitoring
• Ensuring compliance with regulatory standards, quality expectations, and best practices in clinical trial data management
• Collaborating cross-functionally to identify study-level challenges and deliver tailored data-driven solutions

Must have:

• 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, preferably using structured frameworks such as golem, with a solid understanding of modular architecture and functional programming practices.
• Proven proficiency in one or more R visualization and reporting packages, such as shiny, R Markdown.
• Solid data wrangling skills in R, with hands-on experience 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, with a focus on reusability, robustness, and collaborative development.
• Familiarity with version control workflows, including Git and working within a central code repository.
• Full professional proficiency in English
• Strong analytical and logical thinking
• Communication and collaboration skills

Nice to have:

• Experience in data engineering area including one or more of the following: relationship databases, data warehousing, data schemas, data stores, data modeling
• Experience in R Shiny frontend customization using CSS and JavaScript for enhanced user interface and interactivity.
• Object-oriented programming for R ~ R6 (R)
• Azure Services: DevOps, Synapse
• Atlassian Products: Jira, Confluence
• Experience with CluePoints RBM system
• Knowledge of statistical methodsand techniques for analyzing data
• Experienceusing Machine Learning technics andproducts testing and validation

What we offer:

• We value your time so the recruitment process is as quick as 3 meetings
• We'll prepare you to do your job at highest quality level with our extensive onboarding and mentorship program
• You'll have excellent working conditions - spacious and modern office in convenient location, and friendly, supportive team who love to hang out together
• You'll havepermanent work agreement at a stable, privately owned company
• We care about our employees - aside from competitive salary, you'll have good work-life balance with flexible working hours and additional days off, life and medical insurance, sports card, lunch card
• We're constantly growing which meansopportunities for personal and professional growth

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

Please submit your CV in English

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Actual position's title: Clinical Data Scientist

Reporting to the Clinical Data Science Manager, the Clinical Data Scientist is an integral part of our team here at PSI. You will work with clinical trials patient and operational data, develop new data solutions and set up Risk-based Monitoring systems in Process Improvement department.

• Setting up and maintaining risk-based monitoring (RBM) systems and analytical tools in collaboration with Central Monitoring Managers and Medical teams. Developing and programming Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and Tables, Figures, and Listings (TFLs) to enable proactive trial oversight
• Programming and maintaining interactive dashboards and Patient Profiles using R and R Shiny to visualize clinical trial data and support medical review and risk assessment
• Participating in managing and transforming complex datasets from multiple sources and integrating them into the PSI data platform for analysis
• Advising on and contributing to the development of new tools and methodologies for clinical trial analytics and risk-based monitoring
• Ensuring compliance with regulatory standards, quality expectations, and best practices in clinical trial data management
• Collaborating cross-functionally to identify study-level challenges and deliver tailored data-driven solutions

Must have:

• 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, preferably using structured frameworks such as golem, with a solid understanding of modular architecture and functional programming practices.
• Proven proficiency in one or more R visualization and reporting packages, such as shiny, R Markdown.
• Solid data wrangling skills in R, with hands-on experience 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, with a focus on reusability, robustness, and collaborative development.
• Familiarity with version control workflows, including Git and working within a central code repository.
• Full professional proficiency in English
• Strong analytical and logical thinking
• Communication and collaboration skills

Nice to have:

• Experience in data engineering area including one or more of the following: relationship databases, data warehousing, data schemas, data stores, data modeling
• Object-oriented programming for R ~ R6 (R)
• Atlassian Products: Jira, Confluence
• Experience with CluePoints RBM system
• Knowledge of statistical methodsand techniques for analyzing data
• Experienceusing Machine Learning technics andproducts testing and validation

What we offer:

• We value your time so the recruitment process is as quick as 3 meetings
• We'll prepare you to do your job at highest quality level with our extensive onboarding and mentorship program
• You'll have excellent working conditions - spacious and modern office in convenient location, and friendly, supportive team who love to hang out together
• You'll havepermanent work agreement at a stable, privately owned company
• We care about our employees - aside from competitive salary, you'll have good work-life balance with flexible working hours and additional days off, life and medical insurance, sports card, lunch card
• We're constantly growing which meansopportunities for personal and professional growth

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Actual position's title: Clinical Data Scientist

Reporting to the Clinical Data Science Manager, the Clinical Data Scientist is an integral part of our team here at PSI. You will work with clinical trials patient and operational data, develop new data solutions and set up Risk-based Monitoring systems in Process Improvement department. Hybrid work in Milan.

• Setting up and maintaining risk-based monitoring (RBM) systems and analytical tools in collaboration with Central Monitoring Managers and Medical teams. Developing and programming Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and Tables, Figures, and Listings (TFLs) to enable proactive trial oversight
• Programming and maintaining interactive dashboards and Patient Profiles using R and R Shiny to visualize clinical trial data and support medical review and risk assessment
• Participating in managing and transforming complex datasets from multiple sources and integrating them into the PSI data platform for analysis
• Advising on and contributing to the development of new tools and methodologies for clinical trial analytics and risk-based monitoring
• Ensuring compliance with regulatory standards, quality expectations, and best practices in clinical trial data management
• Collaborating cross-functionally to identify study-level challenges and deliver tailored data-driven solutions

• 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, preferably using structured frameworks such as golem, with a solid understanding of modular architecture and functional programming practices.
• Proven proficiency in one or more R visualization and reporting packages, such as shiny, R Markdown.
• Solid data wrangling skills in R, with hands-on experience 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, with a focus on reusability, robustness, and collaborative development.
• Familiarity with version control workflows, including Git and working within a central code repository.
• Full professional proficiency in English
• Strong analytical and logical thinking
• Communication and collaboration skills

• Experience in data engineering area including one or more of the following: relationship databases, data warehousing, data schemas, data stores, data modeling
• Experience in R Shiny frontend customization using CSS and JavaScript for enhanced user interface and interactivity.
• Object-oriented programming for R : R6 (R)
• 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 technics and products testing and validation

• We value your time so the recruitment process is as quick as 3 meetings
• We'll prepare you to do your job at highest quality level with our extensive onboarding and mentorship program
• You'll have excellent working conditions - spacious and modern office in convenient location, and friendly, supportive team who love to hang out together
• You'll have permanent work agreement at a stable, privately owned company
• We care about our employees - aside from competitive salary, you'll have good work-life balance with flexible working hours and additional days off, life and medical insurance, sports card, lunch card
• We're constantly growing which means opportunities for personal and professional growth

Please submit your CV in English.

• Associate

• Full-time

• Analyst

• Pharmaceutical Manufacturing

As a Clinical Research Medical Advisor, you will play a key role in providing clinical, strategic, and tactical leadership to support trials and clinical development plans with medical/clinical accountability, directly impacting the efficiency of clinical trial conduct.

Your key responsibilities

• Manage studies from a medical/clinical perspective, demonstrating the ability to solve problems and mediate complex clinical/medical issues.
• Adapt quickly across different therapeutic areas and indications.
• Lead through effective communication, proactive cross-functional collaboration, and maintain high energy and motivation.
• Provide clinical development and indication expertise, collaborating closely with the Clinical Operations Organization to ensure fast trial startup, recruitment according to timelines, early identification of delays, and robust recruitment mitigation plans.
• Review and resolve local medical issues/questions, supporting discussions with global teams if necessary.

What you’ll bring to the role:

• Medical Degree (preferred)
• Experience in hematology or neuroscience is preferred
• Experience in clinical development
• Proficiency in Italian and English

Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives. We aim to become the most valued and trusted medicines company in the world, driven by our people. Join us in this mission! Learn more at our website .

You’ll receive: Details about our benefits and rewards are available in the Novartis Life Handbook: .

Commitment to Diversity and Inclusion: Novartis is dedicated to building an inclusive, diverse work environment that reflects the communities we serve.

Join our Novartis Network: If this role isn't suitable but you'd like to stay connected and learn about other opportunities, join our network here: .

Why Novartis: Helping people with disease requires more than science; it requires a community of passionate, collaborative individuals. Join us to create a brighter future. Learn more at our website .

Stay Connected: Not the right role now? Sign up to our talent community to hear about future opportunities: .

Job Description Summary

Job Description

Your key responsibilities

Your responsibilities include, but are not limited to:

• Ability to manage a study from the medical/clinical perspective, and a demonstrated capability to solve problems and mediate complex clinical/medical issues.

• Agility to move fast across different therapeutic areas and indications.

• Ability to lead through effective and constructive communication, proactive cross-functional collaboration, strong energy and motivation.

• Provide clinical development and indication expertise and closely collaborates with the Clinical Operation Organization to ensure fast clinical trial start up, recruitment according to planned timelines, early identification of potential delays and robust recruitment mitigation plan.

• Review and resolution of local medical issues / questions – if necessary, support the discussion of issues to global teams.

What you’ll bring to the role:

• Medical Degree (preferred)

• Previous experience in neurosciences will be preferred

• Previous experience in clinical development

• Proficient in Italian and English.

Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here:

You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook ( ).

Commitment to Diversity and Inclusion:

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: .

Skills Desired

Join to apply for the Clinical Research Medical Advisor role at Novartis Italia

Join to apply for the Clinical Research Medical Advisor role at Novartis Italia

Summary

As a Clinical Research Medical Advisor you will play a key role in providing clinical, strategic and tactical leadership to support trials and clinical development plans with a medical / clinical accountability and direct impact on the efficiency of clinical trial conduct.

Summary

As a Clinical Research Medical Advisor you will play a key role in providing clinical, strategic and tactical leadership to support trials and clinical development plans with a medical / clinical accountability and direct impact on the efficiency of clinical trial conduct.

About The Role

Your key responsibilities

Your Responsibilities Include, But Are Not Limited To

• Ability to manage a study from the medical/clinical perspective, and a demonstrated capability to solve problems and mediate complex clinical/medical issues.
• Agility to move fast across different therapeutic areas and indications.
• Ability to lead through effective and constructive communication, proactive cross-functional collaboration, strong energy and motivation.
• Provide clinical development and indication expertise and closely collaborates with the Clinical Operation Organization to ensure fast clinical trial start up, recruitment according to planned timelines, early identification of potential delays and robust recruitment mitigation plan.
• Review and resolution of local medical issues / questions – if necessary, support the discussion of issues to global teams.
  
  

• Medical Degree (preferred)
• Previous experience in hematology or neuroscience will be preferred
• Previous experience in clinical development
• Proficient in Italian and English.
  
  

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Health Care Provider
• Industries Pharmaceutical Manufacturing

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