Junior Statistical SAS Programmer

JR Italy; Bari; In loco; EUR 30.000 - 50.000; Tempo pieno

Descrizione del lavoro

Join a forward-thinking international CRO as a Junior Statistical SAS Programmer, where you will play a crucial role in developing SAS programs for clinical studies and publications. This position offers the opportunity to collaborate with Biostatistics and Data Management teams, ensuring compliance with industry standards while contributing to innovative research. With a focus on professional development, you will thrive in a dynamic environment that values teamwork and excellence. If you are passionate about statistics and programming, this role provides a fantastic platform to advance your career in the pharmaceutical industry.

Servizi

Competitive Salary

Bonuses

Benefits

Professional Development Opportunities

Competenze

• 1+ years of experience in CRO, biotech, or pharma.
• Proficient in SAS and CDISC standards.

Mansioni

• Develop SAS programs for clinical trials and publications.
• Validate ADaM datasets and maintain documentation.

Conoscenze

SAS Programming

CDISC Standards

Statistical Analysis

Data Management

Organizational Skills

Formazione

Bachelor's Degree in Statistics or related field

Strumenti

Pinnacle 21

Descrizione del lavoro

Job Title: Junior Statistical SAS Programmer

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, publications, or Health Authorities requests. The role involves collaboration with Biostatistics and Data Management teams on clinical trials and projects.

Key Responsibilities:

1. Develop SAS programs for generating datasets, tables, figures, and listings for clinical trials, publications, and Health Authorities requests.
2. Utilize 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 validation documents.
7. Liaise with Data Management to develop SAS programs/macros and utilities to detect data discrepancies.
8. Develop SAS programs to import and reconcile external clinical data.
9. Create and validate SAS programs for identifying Non-Protocol Deviations.
10. Maintain SAS programming documentation.
11. Establish and maintain SOPs and related templates for Statistical SAS programming.
12. Stay informed on new SAS developments relevant to clinical data management and update the Direct Manager accordingly.
13. Ensure KPIs and metrics for assigned studies are met.
14. Complete all required trainings timely.
15. Accurately complete daily entries in the TRACK system.
16. Perform other assigned tasks as needed.

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:

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

Please review the personal data processing notice available on our website.

About Us:

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, covering all phases of drug-related trials and medical device investigations with global locations and comprehensive services.