9 Posti di lavoro per Clinical Testing in Italia

Eurofins BioPharma Product Testing ricerca per la propria sede di Vimodrone (MI) una risorsa da inserire in qualit di Direttore di Studio presso la divisione Medical Device Testing .

Il Direttore di Studio ha la responsabilit di gestire attivit di studio condotte allinterno del laboratorio di competenza coordinandosi internamente con i tecnici di laboratorio e con gli altri team presenti in azienda.

Nello specifico la risorsa si occuper di :

• Assicurare coordinandosi con il proprio responsabile e colleghi unefficace programmazione e gestione degli studi assegnati;
• Coordinare gli analisti preposti allesecuzione di uno studio di cui responsabile;
• Affiancare i tecnici di laboratorio in caso di necessit per garantire uno svolgimento efficace dello studio;
• Produrre e redigere protocolli e report di studio;
• Garantire una corretta gestione dei dati nel rispetto dei principi GLP.
• Laurea in discipline scientifiche preferibilmente Biotecnologie / Biologia / Ingegneria Biomedica e affini;
• Esperienza pregressa minimo un anno in attivit di coordinamento e gestione di studi / progetti;
• Conoscenza dei principi GLP;
• Ottima conoscenza della lingua inglese (scritta / parlata);
• Domicilio nellarea geografica di riferimento (Vimodrone).

Informazioni aggiuntive :

Per candidarsi necessario inviare Curriculum dettagliato e lettera di presentazione specificando lautorizzazione al trattamento dei dati personali.

Non saranno presi in considerazione CV privi di questi requisiti.

Eurofins BioPharma Product Testing ricerca per la propria sede di Vimodrone (MI) una risorsa da inserire in qualit di Direttore di Studio presso la divisione Medical Device Testing .

Il Direttore di Studio ha la responsabilit di gestire attivit di studio condotte allinterno del laboratorio di competenza coordinandosi internamente con i tecnici di laboratorio e con gli altri team presenti in azienda.

Nello specifico la risorsa si occuper di :

• Assicurare coordinandosi con il proprio responsabile e colleghi unefficace programmazione e gestione degli studi assegnati;
• Coordinare gli analisti preposti allesecuzione di uno studio di cui responsabile;
• Affiancare i tecnici di laboratorio in caso di necessit per garantire uno svolgimento efficace dello studio;
• Produrre e redigere protocolli e report di studio;
• Garantire una corretta gestione dei dati nel rispetto dei principi GLP.
• Laurea in discipline scientifiche preferibilmente Biotecnologie / Biologia / Ingegneria Biomedica e affini;
• Esperienza pregressa minimo un anno in attivit di coordinamento e gestione di studi / progetti;
• Conoscenza dei principi GLP;
• Ottima conoscenza della lingua inglese (scritta / parlata);
• Domicilio nellarea geografica di riferimento (Vimodrone).

Informazioni aggiuntive :

Per candidarsi necessario inviare Curriculum dettagliato e lettera di presentazione specificando lautorizzazione al trattamento dei dati personali.

Non saranno presi in considerazione CV privi di questi requisiti.

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.

Job Description

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

Qualifications

Must have :

Nice to have :

Additional Information

What we offer :

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

J-18808-Ljbffr

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.

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.

Job Description

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

Qualifications

Must have :

Nice to have :

Additional Information

What we offer :

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

J-18808-Ljbffr

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.