Junior Statistical Sas Programmer

Buscojobs; Lombardia; In loco; EUR 30.000 - 60.000; Tempo pieno

Descrizione del lavoro

An innovative international CRO is seeking a Junior Statistical SAS Programmer to join their dynamic team. In this role, you will develop SAS programs for generating critical datasets and reports for clinical studies, ensuring compliance with industry standards. You'll collaborate closely with Biostatistics and Data Management teams, contributing to the success of clinical trials. This opportunity offers a competitive salary, bonuses, and a chance for professional growth in a supportive environment. If you are passionate about data management and clinical research, this position is perfect for you.

Servizi

Competitive Salary

Bonuses

Professional Development Opportunities

Competenze

• At least 1 year of experience in a similar role in CRO, biotech, or pharma.
• Knowledge of HA requirements for pharmaceutical research and SAS programming.

Mansioni

• Develop SAS programs for clinical trials and publications.
• Validate ADaM datasets and prepare CDISC documentation.
• Collaborate with Biostatistics and Data Management teams.

Conoscenze

SAS Programming

CDISC Standards

Statistical Knowledge

Communication Skills

Teamwork

Planning and Organization

Formazione

Scientific Degree

Strumenti

Pinnacle 21

Descrizione del lavoro

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 :

1. Develop SAS programs for generating datasets, tables, figures, and listings for clinical trials (according to ICH E3), publications, or Health Authorities requests.
2. Use CDISC guidelines to generate SDTM / ADaM datasets.
3. Write Programming Specifications of analysis datasets.
4. Validate ADaM datasets using Pinnacle 21.
5. Prepare, maintain, and archive CDISC documentation for ADaM (Define.xml and ADRG).
6. Contribute to developing standard SAS macros and prepare the corresponding validation documents.
7. Liaise with Data Management team and develop SAS programs/macros/utilities to detect discrepancies in the data.
8. Check the requirements to handle external clinical data and develop SAS programs to import/reconcile external clinical data.
9. Develop and validate SAS programs for identification of Non-Protocol Deviations.
10. Collaborate with Biostatistics and Data Management staff on clinical trials/projects.
11. Prepare, maintain, and archive SAS programming documentation.
12. Contribute to establishing and maintaining SOPs and related templates for Statistical SAS programming.
13. Stay informed on new SAS developments relevant to clinical trial data management and update the Direct Manager.
14. Ensure KPI and metrics for assigned studies are met.
15. Complete required trainings on time.
16. Ensure daily completion of TRACK system, with correct entry of billable and non-billable time.
17. Perform other tasks as assigned.

What we're looking for :

• Scientific degree.
• At least 1 year of experience in CRO, biotech, pharma, research institutes in a similar role (preferred).
• Knowledge of HA requirements pertaining to pharmaceutical research and SAS programming.
• Knowledge in statistics and its applications to clinical trials.
• Knowledge of SAS and CDISC standards (SDTM, ADaM).
• Fluent in English.
• Planning and organizational skills.
• Communication skills.
• Team-working orientation.

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 worldwide. We provide state-of-the-art IT solutions and innovative approaches to complex projects. Our expertise spans all phases of drug-related trials and medical device investigations, with global locations offering comprehensive clinical research services.