Junior Statistical SAS Programmer

Opis S.r.l.; Trento; In loco; EUR 30.000 - 45.000; Tempo pieno

Descrizione del lavoro

A leading international CRO seeks a Junior Statistical SAS Programmer to develop SAS programs for clinical trials and assist in data management under the supervision of the Direct Manager. This role demands experience in SAS programming, strong organizational skills, and teamwork. Competitive salary and benefits are offered in a continually expanding company.

Servizi

Competitive salary

Bonuses

Benefits

Opportunities for professional growth

Competenze

• Minimum 1 year of relevant experience in CRO, biotech, or pharma.
• Familiarity with HA requirements on SAS programming.
• Strong understanding of CDISC standards (SDTM, ADaM).

Mansioni

• Develop SAS programs for clinical datasets, tables, and listings.
• Write programming specifications and validate ADaM datasets.
• Maintain SAS programming documentation and establish SOPs.

Conoscenze

Knowledge of statistics

Proficiency in SAS

Team-oriented attitude

Strong planning and organizational skills

Descrizione del lavoro

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

Responsibilities include:

1. Developing SAS programs for datasets, tables, figures, and listings for clinical trials, publications, and health authority requests.
2. Using CDISC guidelines to generate SDTM and ADaM datasets.
3. Writing programming specifications for analysis datasets.
4. Validating ADaM datasets with Pinnacle 21.
5. Preparing, maintaining, and archiving CDISC documentation such as Define.xml and ADRG.
6. Developing standard SAS macros and validation documents.
7. Liaising with Data Management to develop programs and macros to detect data discrepancies.
8. Handling external clinical data and developing import/reconciliation programs.
9. Developing and validating programs for identifying Non-Protocol Deviations.
10. Collaborating with Biostatistics and Data Management teams.
11. Maintaining SAS programming documentation.
12. Establishing and maintaining SOPs and related documentation.
13. Staying informed on new SAS developments relevant to clinical data management.
14. Meeting KPIs and metrics for assigned studies.
15. Completing required trainings on time.
16. Accurately entering data into the TRACK system daily.
17. Performing additional tasks as assigned.

Qualifications:

1. Minimum 1 year of experience in CRO, biotech, pharma, or research institutes in a similar role; knowledge of HA requirements related to SAS programming is preferred.
2. Knowledge of statistics and its application to clinical trials.
3. Proficiency in SAS and CDISC standards (SDTM, ADaM).
4. Strong planning and organizational skills.
5. Team-oriented attitude.

What we offer:

Competitive salary, bonuses, benefits, and opportunities for professional growth within an expanding international company.

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About OPIS:

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 technology and innovative solutions for complex projects across all phases of drug trials, including services like scientific advice, medical writing, trial start-up, monitoring, data management, statistics, pharmacovigilance, and more.

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