Junior Statistical Sas Programmer

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

Descrizione del lavoro

An established industry player is seeking a Junior Statistical SAS Programmer to join their dynamic team. This role involves developing SAS programs for clinical studies, collaborating with biostatistics and data management teams, and ensuring compliance with industry standards. The ideal candidate will possess a scientific degree and at least one year of relevant experience in a CRO or similar environment. This position offers a competitive salary, bonuses, and opportunities for career development in a growing international company dedicated to innovative clinical research solutions.

Servizi

Competitive Salary

Bonuses

Career Development Opportunities

Competenze

• 1+ year experience in CRO, biotech, pharma, or research institutes.
• Proficiency in SAS and CDISC standards essential.

Mansioni

• Develop SAS programs for datasets and listings for clinical trials.
• Collaborate with Biostatistics and Data Management on projects.

Conoscenze

SAS Programming

CDISC Standards (SDTM, ADaM)

Statistical Knowledge

Communication Skills

Planning and Organizational Skills

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, and Health Authorities requests.
2. Use CDISC guidelines to generate SDTM / ADaM datasets.
3. Write Programming Specifications for 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 validation documents.
7. Liaise with Data Management team to develop SAS programs/macros/utilities for discrepancy detection.
8. Handle external clinical data requirements and develop SAS programs to import/reconcile such data.
9. Develop and validate SAS programs for identifying Non-Protocol Deviations.
10. Collaborate with Biostatistics and Data Management staff on clinical trials/projects.
11. Maintain and archive SAS programming documentation.
12. Establish and maintain SOPs, templates, and standards related to SAS programming.
13. Stay informed on new SAS developments relevant to clinical trial data management.
14. Ensure KPIs and metrics are met for assigned studies.
15. Complete required trainings on time.
16. Perform daily entries in the TRACK system accurately.
17. Perform other assigned tasks.

What we're looking for :

• Scientific degree.
• 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 their applications to clinical trials.
• Proficiency in SAS and CDISC standards (SDTM, ADaM).
• Fluency in English.
• Planning and organizational skills.
• Good communication skills.
• Team-oriented mindset.

What we offer :

Competitive salary, bonuses, and benefits, along with career development opportunities in an expanding international company. Please review the personal data processing notice on our website.

Who we are :

OPIS is a 25-year-old international CRO 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, covering all phases of drug trials and medical device investigations, with locations worldwide offering comprehensive clinical research services.