Junior Statistical Sas Programmer

Buscojobs; Piemonte; In loco; EUR 30.000 - 45.000; Tempo pieno

Descrizione del lavoro

A leading international CRO is seeking a Junior Statistical SAS Programmer to develop SAS programs for clinical studies. The role involves collaboration with Biostatistics and Data Management, ensuring compliance with ICH E3 and CDISC standards. The candidate will contribute to various programming tasks, maintain documentation, and support the team in clinical trials. This position offers opportunities for professional development in a growing company.

Servizi

Competitive Salary

Bonuses

Professional Development Opportunities

Competenze

• At least 1 year of experience in CRO, biotech, pharma, or research institutes.
• Knowledge of HA requirements and SAS programming.
• Fluent in English.

Mansioni

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

Conoscenze

Statistics

Communication

Planning

Organizational Skills

Teamwork

Formazione

Scientific Degree

Strumenti

SAS

CDISC

Descrizione del lavoro

Junior Statistical SAS Programmer

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 the corresponding validation documents.
7. Liaise with Data Management team and develop SAS programs/macros/utilities to detect data discrepancies.
8. Check requirements to handle external clinical data and develop SAS programs to import/reconcile external 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. Maintain and archive SAS programming documentation.
12. Assist in establishing and maintaining SOPs, forms, and templates related to Statistical SAS programming.
13. Contribute to developing and maintaining document/programming standards.
14. Stay informed on new SAS developments relevant to clinical trial data management and promptly update the Direct Manager.
15. Ensure KPI and metrics for assigned studies are met.
16. Complete all required trainings on time (study trainings, OPIS SOPs, and other applicable trainings).
17. Ensure daily completion of the TRACK system and correct entry of billable/non-billable time.
18. Perform any other tasks as assigned.

What we're looking for:

• Scientific degree.
• At least 1 year of experience in CRO, biotech, pharma, or research institutes in a similar role is 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.
• Excellent communication skills.
• Team-oriented mentality.

What we offer:

We offer a competitive salary, bonuses, and other benefits, along with the opportunity to develop your professional career within an expanding and growing international company. Please read the information notice on the processing of personal data in the candidates’ information section of 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 state-of-the-art information technology solutions and innovative approaches to handle increasing project complexity.

Our extensive expertise covers all phases of drug-related trials, supporting Sponsors across various therapeutic areas, including clinical investigations for medical and diagnostic devices. With global clinical research locations, OPIS offers comprehensive services including scientific advice, medical writing, trial start-up, monitoring, study management, data management, statistics, pharmacovigilance, medical monitoring, electronic data capture, quality assurance, and training.