416 Posti di lavoro per Sas Programmer in Italia

• Responsible for importing, cleaning, transforming, and validating data to ensure its accuracy and integrity for analysis.


• Using SAS procedures and functions to perform various statistical analyses such as descriptive statistics, hypothesis testing, regression analysis, and predictive modeling.


• Create reports, tables, and graphs to present analysis results in a clear and understandable format for stakeholders.


• Write and debug SAS code to automate data processing tasks, perform complex analyses, and generate reports efficiently.


• Collaborate with other team members such as statisticians, data scientists, and business analysts to understand project requirements and deliver actionable insights.

• Strong understanding of SAS programming language and its various procedures (e.g., PROC SQL, PROC REG, PROC MEANS) is essential.


• Familiarity with statistical concepts and techniques is necessary for conducting meaningful analyses and interpreting results accurately.


• Experience with data manipulation, cleansing, and validation techniques for working with diverse datasets.


• Attention to detail is crucial to avoid errors in analysis and reporting.


• Strong problem-solving skills to address data-related challenges and optimize analysis processes.


• A bachelor’s or master’s degree in a quantitative field such as statistics, mathematics, computer science, or a related discipline.

The Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is mainly involved in developing SAS programs for the generation of datasets, tables, figures, and listings for clinical studies (according to ICH E3), publications, or Health Authorities requests. Collaborates with Biostatistics and Data Management staff on clinical trials/projects.

Some of what you'll do :

• Develop SAS programs for generating datasets, tables, figures, and listings for clinical trials (according to ICH E3), publications, or Health Authorities requests.
• Use CDISC guidelines to generate SDTM / ADaM datasets.
• Write Programming Specifications for analysis datasets.
• Validate ADaM datasets using Pinnacle 21.
• Prepare, maintain, and archive CDISC documentation for ADaM (Define.xml and ADRG).
• Contribute to developing standard SAS macros and prepare validation documents.
• Liaise with Data Management team to develop SAS programs/macros/utilities to detect data discrepancies.
• Develop SAS programs to handle external clinical data, including import/reconciliation processes.
• Develop and validate SAS programs for identifying Non-Protocol Deviations.
• Collaborate with Biostatistics and Data Management staff on clinical trials/projects.
• Maintain and archive SAS programming documentation.
• Assist in establishing and maintaining SOPs and templates related to Statistical SAS programming.
• Stay informed on new SAS developments relevant to clinical trial data management and update the Direct Manager.
• Ensure KPIs and metrics for assigned studies are met.
• Complete required trainings on time.
• Accurately record daily work hours in the TRACK system.
• Perform other tasks as assigned.

What we're looking for :

• At least 1 year of experience in CRO, biotech, pharma, or research institutes in a similar role is preferred.
• Knowledge of HA requirements related to pharmaceutical research and SAS programming.
• Knowledge of statistics and its applications to clinical trials.
• Proficiency in SAS and CDISC standards (SDTM, ADaM).
• Strong planning and organizational skills.
• Team-oriented mindset.

What we offer :

We offer a competitive salary, bonuses, and other benefits, along with opportunities for professional development within an expanding international company.

Please review the personal data processing notice on our website.

Who we are :

OPIS is an international CRO with 25 years of experience in conducting Phase I-IV, non-interventional, and medical device studies globally. We provide state-of-the-art IT solutions and innovative approaches to complex projects.

Our expertise spans all phases of drug trials, supporting sponsors beyond therapeutic areas, including clinical investigations for medical and diagnostic devices. With global locations, we offer comprehensive clinical research services, including scientific advice, medical writing, trial start-up, monitoring, data management, statistics, pharmacovigilance, medical monitoring, electronic data capture, quality assurance, and training.

J-18808-Ljbffr

The Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is mainly involved in developing SAS programs for the generation of datasets, tables, figures and listings for clinical studies (according to ICH E3), publications or Health Authorities requests. Collaborates with Biostatistics and Data Management staff on clinical trials/projects.

Some of what you'll do:

• Develop SAS programs for generating datasets, tables, figures and listings for clinical trials (according to ICH E3) and/or publication, and/or Health Authorities requests
• Use CDISC guidelines to generate SDTM/ADaM datasets
• Write Programming Specifications of analysis datasets
• Validate ADaM datasets using Pinnacle 21
• Prepare, maintain, and archive CDISC documentation for ADaM (Define.xml and ADRG)
• Contribute to developing standard SAS macros and prepare the corresponding validation documents
• Liaise with Data Management team and develop SAS programs/macros and utilities to detect discrepancies in the data
• Check the requirements to handle external clinical data and develop the SAS programs to import/reconcile external clinical data
• Develop and validate SAS programs for identification of Non-Protocol Deviations
• Collaborate with Biostatistics and Data Management staff on clinical trials/projects
• Prepare, maintain and archive SAS programming documentation
• Collaborate in establishing and maintaining standard operating procedures (SOPs) and corresponding forms/templates related to Statistical SAS programming
• Collaborate in establishing and maintaining document/programming standards
• Keep informed on new SAS developments relevant to the clinical trial data management promptly updating the Direct Manager
• Ensure that KPI and metrics for the assigned studies are met
• Perform and complete on time all required trainings (study trainings, training on OPIS and/or Sponsor SOPs, all other applicable trainings) by the assigned due date
• Ensure daily completion of TRACK system, correct entry of appropriate billable and non-billable time
• Perform other tasks as assigned

What we're looking for:

• At least 1 year of experience in CRO, biotech, pharma, research institutes in similar role is preferred Knowledge of HA requirements pertaining to pharmaceutical research and specifically to SAS programming
• Knowledge in statistics and its applications to clinical trials
• Knowledge of SAS and CDISC standards (SDTM, ADaM)
• Planning and organizational skills
• Team-working oriented

What we offer:

We offer a competitive salary, bonuses, and other benefits together with the opportunity to develop your professional career with an expanding and growing international company.

Please read the information notice on the processing of personal data in the candidates’ information section of our company website.

Who we are:

OPIS is an International CRO with 25 years of experience in conducting Phase I-IV, non-interventional and medical devices studies on an international level. We always offer state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of projects.

OPIS extensive expertise covers all phases of drug-related trials, taking care of the Sponsor beyond the therapeutic area, offering also accurate clinical investigations for medical and diagnostic devices. With Global Clinical Research Locations all over the world, OPIS offers a full range of integrated clinical research services as scientific advice, medical writing, trial start-up, monitoring, study management, data management, statistics, pharmacovigilance, medical monitoring, electronic data capture as well as quality assurance and training.

I accept the Candidate Privacy Policy, and I authorize the processing of my special categories of Personal Data (necessary if contained in the CV)* I accept

The Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is primarily responsible for developing SAS programs to generate datasets, tables, figures, and listings for clinical studies (according to ICH E3), publications, or Health Authorities requests. The role involves collaboration with Biostatistics and Data Management staff on clinical trials and projects.

Responsibilities include:

• Developing SAS programs for datasets, tables, figures, and listings for clinical trials, publications, and Health Authorities requests.
• Using CDISC guidelines to generate SDTM / ADaM datasets.
• Writing programming specifications for analysis datasets.
• Validating ADaM datasets using Pinnacle 21.
• Preparing, maintaining, and archiving CDISC documentation for ADaM (Define.xml and ADRG).
• Developing standard SAS macros and validation documents.
• Liaising with Data Management to develop SAS programs, macros, and utilities to detect data discrepancies.
• Handling external clinical data and developing SAS programs for data import and reconciliation.
• Developing and validating SAS programs for identifying Non-Protocol Deviations.
• Collaborating with Biostatistics and Data Management teams on clinical projects.
• Establishing and maintaining SOPs, forms, and templates related to SAS programming.
• Staying informed on new SAS developments relevant to clinical data management.
• Ensuring KPIs and metrics are met for assigned studies.
• Completing required trainings on time.
• Accurately entering data into the TRACK system daily.
• Performing additional tasks as assigned.

Qualifications:

• At least 1 year of experience in CRO, biotech, pharma, or research institutes in a similar role is preferred.
• Knowledge of HA requirements related to pharmaceutical research and SAS programming.
• Understanding of statistics and its application to clinical trials.
• Proficiency in SAS and CDISC standards (SDTM, ADaM).
• Strong planning and organizational skills.
• Team-oriented attitude.

What we offer:

A competitive salary, bonuses, and benefits, along with opportunities for professional development within an expanding international company.

Please review the personal data processing notice on our website.

Who we are:

OPIS is a global CRO with 25 years of experience in conducting Phase I-IV studies, non-interventional, and medical device trials worldwide. We provide state-of-the-art technology and innovative solutions for complex projects, covering all phases of drug-related trials and medical device investigations.

With global locations, we offer comprehensive clinical research services, including scientific advice, medical writing, trial start-up, monitoring, data management, statistics, pharmacovigilance, medical monitoring, electronic data capture, quality assurance, and training.

I accept the Candidate Privacy Policy and authorize processing of my personal data as necessary.

The Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is primarily responsible for developing SAS programs to generate datasets, tables, figures, and listings for clinical studies (according to ICH E3), publications, or Health Authorities requests. The role involves collaboration with Biostatistics and Data Management staff on clinical trials and projects.

Responsibilities include:

• Developing SAS programs for datasets, tables, figures, and listings for clinical trials, publications, and Health Authorities requests.
• Using CDISC guidelines to generate SDTM / ADaM datasets.
• Writing programming specifications for analysis datasets.
• Validating ADaM datasets using Pinnacle 21.
• Preparing, maintaining, and archiving CDISC documentation for ADaM (Define.xml and ADRG).
• Developing standard SAS macros and validation documents.
• Liaising with Data Management to develop SAS programs, macros, and utilities to detect data discrepancies.
• Handling external clinical data and developing SAS programs for data import and reconciliation.
• Developing and validating SAS programs for identifying Non-Protocol Deviations.
• Collaborating with Biostatistics and Data Management teams on clinical projects.
• Maintaining SAS programming documentation.
• Establishing and maintaining SOPs, forms, and templates related to SAS programming.
• Staying informed on new SAS developments relevant to clinical data management.
• Ensuring KPIs and metrics are met for assigned studies.
• Completing required trainings on time.
• Accurately entering data into the TRACK system daily.
• Performing additional tasks as assigned.

Qualifications:

• At least 1 year of experience in CRO, biotech, pharma, or research institutes in a similar role is preferred.
• Knowledge of HA requirements related to pharmaceutical research and SAS programming.
• Understanding of statistics and its application to clinical trials.
• Proficiency in SAS and CDISC standards (SDTM, ADaM).
• Strong planning and organizational skills.
• Team-oriented attitude.

What we offer:

A competitive salary, bonuses, and benefits, along with opportunities for professional development within an expanding international company.

Please review the personal data processing notice on our website.

Who we are:

OPIS is a global CRO with 25 years of experience in conducting Phase I-IV studies, non-interventional, and medical device trials worldwide. We provide state-of-the-art technology and innovative solutions for complex projects, covering all phases of drug-related trials and medical device investigations.

With global locations, we offer comprehensive clinical research services, including scientific advice, medical writing, trial start-up, monitoring, data management, statistics, pharmacovigilance, medical monitoring, electronic data capture, quality assurance, and training.

I accept the Candidate Privacy Policy and authorize processing of my personal data as necessary.

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02.05.2025

16.06.2025

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The Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is mainly involved in developing SAS programs for the generation of datasets, tables, figures and listings for clinical studies (according to ICH E3), publications or Health Authorities requests. Collaborates with Biostatistics and Data Management staff on clinical trials/projects.

Some of what you'll do:

• Develop SAS programs for generating datasets, tables, figures and listings for clinical trials (according to ICH E3) and/or publication, and/or Health Authorities requests
• Use CDISC guidelines to generate SDTM/ADaM datasets
• Write Programming Specifications of analysis datasets
• Validate ADaM datasets using Pinnacle 21
• Prepare, maintain, and archive CDISC documentation for ADaM (Define.xml and ADRG)
• Contribute to developing standard SAS macros and prepare the corresponding validation documents
• Liaise with Data Management team and develop SAS programs/macros and utilities to detect discrepancies in the data
• Check the requirements to handle external clinical data and develop the SAS programs to import/reconcile external clinical data
• Develop and validate SAS programs for identification of Non-Protocol Deviations
• Collaborate with Biostatistics and Data Management staff on clinical trials/projects
• Prepare, maintain and archive SAS programming documentation
• Collaborate in establishing and maintaining standard operating procedures (SOPs) and corresponding forms/templates related to Statistical SAS programming
• Collaborate in establishing and maintaining document/programming standards
• Keep informed on new SAS developments relevant to the clinical trial data management promptly updating the Direct Manager
• Ensure that KPI and metrics for the assigned studies are met
• Perform and complete on time all required trainings (study trainings, training on OPIS and/or Sponsor SOPs, all other applicable trainings) by the assigned due date
• Ensure daily completion of TRACK system, correct entry of appropriate billable and non-billable time
• Perform other tasks as assigned

What we're looking for:

• At least 1 year of experience in CRO, biotech, pharma, research institutes in similar role is preferred Knowledge of HA requirements pertaining to pharmaceutical research and specifically to SAS programming
• Knowledge in statistics and its applications to clinical trials
• Knowledge of SAS and CDISC standards (SDTM, ADaM)
• Planning and organizational skills
• Team-working oriented

What we offer:

We offer a competitive salary, bonuses, and other benefits together with the opportunity to develop your professional career with an expanding and growing international company.

Please read the information notice on the processing of personal data in the candidates’ information section of our company website.

Who we are:

OPIS is an International CRO with 25 years of experience in conducting Phase I-IV, non-interventional and medical devices studies on an international level. We always offer state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of projects.

OPIS extensive expertise covers all phases of drug-related trials, taking care of the Sponsor beyond the therapeutic area, offering also accurate clinical investigations for medical and diagnostic devices. With Global Clinical Research Locations all over the world, OPIS offers a full range of integrated clinical research services as scientific advice, medical writing, trial start-up, monitoring, study management, data management, statistics, pharmacovigilance, medical monitoring, electronic data capture as well as quality assurance and training.

The Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is mainly involved in developing SAS programs for the generation of datasets, tables, figures, and listings for clinical studies (according to ICH E3), publications, or Health Authorities requests. Collaborates with Biostatistics and Data Management staff on clinical trials/projects.

Some of what you'll do :

• Develop SAS programs for generating datasets, tables, figures, and listings for clinical trials (according to ICH E3), publications, or Health Authorities requests.
• Use CDISC guidelines to generate SDTM / ADaM datasets.
• Write Programming Specifications for analysis datasets.
• Validate ADaM datasets using Pinnacle 21.
• Prepare, maintain, and archive CDISC documentation for ADaM (Define.xml and ADRG).
• Contribute to developing standard SAS macros and prepare validation documents.
• Liaise with Data Management team to develop SAS programs/macros/utilities to detect data discrepancies.
• Handle external clinical data and develop SAS programs to import/reconcile it.
• Develop and validate SAS programs for identifying Non-Protocol Deviations.
• Collaborate with Biostatistics and Data Management staff on clinical trials/projects.
• Maintain and archive SAS programming documentation.
• Assist in establishing and maintaining SOPs and related documentation for SAS programming.
• Stay informed on new SAS developments relevant to clinical trial data management.
• Ensure KPI and metrics for assigned studies are met.
• Complete required trainings on time.
• Accurately complete daily entries in the TRACK system.
• Perform other tasks as assigned.

What we're looking for :

• At least 1 year of experience in CRO, biotech, pharma, or research institutes in a similar role (preferred).
• Knowledge of HA requirements related to pharmaceutical research and SAS programming.
• Knowledge of statistics and its applications to clinical trials.
• Knowledge of SAS and CDISC standards (SDTM, ADaM).
• Planning and organizational skills.
• Team-oriented attitude.

What we offer :

We offer a competitive salary, bonuses, and benefits, along with opportunities for professional development within an expanding international company.

Please review the personal data processing notice on our website.

Who we are :

OPIS is an international CRO with 25 years of experience conducting Phase I-IV, non-interventional, and medical device studies worldwide. We provide cutting-edge IT solutions and innovative approaches to complex projects.

Our expertise spans all phases of drug trials, supporting sponsors across therapeutic areas and offering comprehensive clinical research services, including medical advice, writing, trial start-up, monitoring, data management, statistics, pharmacovigilance, and more.

J-18808-Ljbffr

The Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is mainly involved in developing SAS programs for the generation of datasets, tables, figures and listings for clinical studies (according to ICH E3), publications or Health Authorities requests. Collaborates with Biostatistics and Data Management staff on clinical trials/projects.

Some of what you'll do:

• Develop SAS programs for generating datasets, tables, figures and listings for clinical trials (according to ICH E3) and/or publication, and/or Health Authorities requests
• Use CDISC guidelines to generate SDTM/ADaM datasets
• Write Programming Specifications of analysis datasets
• Validate ADaM datasets using Pinnacle 21
• Prepare, maintain, and archive CDISC documentation for ADaM (Define.xml and ADRG)
• Contribute to developing standard SAS macros and prepare the corresponding validation documents
• Liaise with Data Management team and develop SAS programs/macros and utilities to detect discrepancies in the data
• Check the requirements to handle external clinical data and develop the SAS programs to import/reconcile external clinical data
• Develop and validate SAS programs for identification of Non-Protocol Deviations
• Collaborate with Biostatistics and Data Management staff on clinical trials/projects
• Prepare, maintain and archive SAS programming documentation
• Collaborate in establishing and maintaining standard operating procedures (SOPs) and corresponding forms/templates related to Statistical SAS programming
• Collaborate in establishing and maintaining document/programming standards
• Keep informed on new SAS developments relevant to the clinical trial data management promptly updating the Direct Manager
• Ensure that KPI and metrics for the assigned studies are met
• Perform and complete on time all required trainings (study trainings, training on OPIS and/or Sponsor SOPs, all other applicable trainings) by the assigned due date
• Ensure daily completion of TRACK system, correct entry of appropriate billable and non-billable time
• Perform other tasks as assigned

What we're looking for:

• At least 1 year of experience in CRO, biotech, pharma, research institutes in similar role is preferred Knowledge of HA requirements pertaining to pharmaceutical research and specifically to SAS programming
• Knowledge in statistics and its applications to clinical trials
• Knowledge of SAS and CDISC standards (SDTM, ADaM)
• Planning and organizational skills
• Team-working oriented

What we offer:

We offer a competitive salary, bonuses, and other benefits together with the opportunity to develop your professional career with an expanding and growing international company.

Please read the information notice on the processing of personal data in the candidates’ information section of our company website.

Who we are:

OPIS is an International CRO with 25 years of experience in conducting Phase I-IV, non-interventional and medical devices studies on an international level. We always offer state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of projects.

OPIS extensive expertise covers all phases of drug-related trials, taking care of the Sponsor beyond the therapeutic area, offering also accurate clinical investigations for medical and diagnostic devices. With Global Clinical Research Locations all over the world, OPIS offers a full range of integrated clinical research services as scientific advice, medical writing, trial start-up, monitoring, study management, data management, statistics, pharmacovigilance, medical monitoring, electronic data capture as well as quality assurance and training.

I accept the Candidate Privacy Policy, and I authorize the processing of my special categories of Personal Data (necessary if contained in the CV)* I accept

The Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is mainly involved in developing SAS programs for the generation of datasets, tables, figures, and listings for clinical studies (according to ICH E3), publications, or Health Authorities requests. Collaborates with Biostatistics and Data Management staff on clinical trials/projects.

Some of what you'll do :

• Develop SAS programs for generating datasets, tables, figures, and listings for clinical trials (according to ICH E3), publications, or Health Authorities requests.
• Use CDISC guidelines to generate SDTM / ADaM datasets.
• Write Programming Specifications for analysis datasets.
• Validate ADaM datasets using Pinnacle 21.
• Prepare, maintain, and archive CDISC documentation for ADaM (Define.xml and ADRG).
• Contribute to developing standard SAS macros and prepare validation documents.
• Liaise with Data Management team to develop SAS programs/macros/utilities to detect data discrepancies.
• Develop SAS programs to handle external clinical data, including import/reconciliation processes.
• Develop and validate SAS programs for identifying Non-Protocol Deviations.
• Collaborate with Biostatistics and Data Management staff on clinical trials/projects.
• Maintain and archive SAS programming documentation.
• Assist in establishing and maintaining SOPs and templates related to Statistical SAS programming.
• Stay informed on new SAS developments relevant to clinical trial data management and update the Direct Manager.
• Ensure KPIs and metrics for assigned studies are met.
• Complete required trainings on time.
• Accurately record daily work hours in the TRACK system.
• Perform other tasks as assigned.

What we're looking for :

• At least 1 year of experience in CRO, biotech, pharma, or research institutes in a similar role is preferred.
• Knowledge of HA requirements related to pharmaceutical research and SAS programming.
• Knowledge of statistics and its applications to clinical trials.
• Proficiency in SAS and CDISC standards (SDTM, ADaM).
• Strong planning and organizational skills.
• Team-oriented mindset.

What we offer :

We offer a competitive salary, bonuses, and other benefits, along with opportunities for professional development within an expanding international company.

Please review the personal data processing notice on our website.

Who we are :

OPIS is an international CRO with 25 years of experience in conducting Phase I-IV, non-interventional, and medical device studies globally. We provide state-of-the-art IT solutions and innovative approaches to complex projects.

Our expertise spans all phases of drug trials, supporting sponsors beyond therapeutic areas, including clinical investigations for medical and diagnostic devices. With global locations, we offer comprehensive clinical research services, including scientific advice, medical writing, trial start-up, monitoring, data management, statistics, pharmacovigilance, medical monitoring, electronic data capture, quality assurance, and training.

J-18808-Ljbffr