Junior Statistical Sas Programmer

Buscojobs; Lazio; In loco; EUR 30.000 - 55.000; Tempo pieno

Descrizione del lavoro

An established industry player seeks a Junior Statistical SAS Programmer to join their dynamic team. In this role, you will develop SAS programs crucial for generating datasets and reports for clinical studies, ensuring compliance with ICH E3 guidelines. You will collaborate closely with Biostatistics and Data Management teams, contributing to the success of clinical trials. This position offers a competitive salary and benefits, along with opportunities for professional growth in a supportive and innovative environment. If you are passionate about statistics and programming, this is the perfect opportunity to advance your career.

Servizi

Competitive Salary

Bonuses

Professional Growth Opportunities

Comprehensive Benefits

Competenze

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

Mansioni

• Develop SAS programs for clinical trials and publications.
• Collaborate with Biostatistics and Data Management teams.

Conoscenze

SAS Programming

CDISC Standards

Statistical Knowledge

Planning and Organization

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 in accordance with ICH E3 guidelines. The role involves collaboration with Biostatistics and Data Management teams on clinical trials and projects.

Key Responsibilities:

1. Develop SAS programs for creating datasets, tables, figures, and listings for clinical trials, publications, and Health Authorities requests.
2. Use CDISC guidelines to generate SDTM and ADaM datasets.
3. Write programming specifications for analysis datasets.
4. Validate ADaM datasets using Pinnacle 21.
5. Prepare, maintain, and archive CDISC documentation such as Define.xml and ADRG for ADaM datasets.
6. Contribute to developing standard SAS macros and validation documents.
7. Liaise with Data Management team to develop SAS programs, macros, and utilities for data discrepancy detection.
8. Handle external clinical data requirements and develop SAS programs for data import and reconciliation.
9. Develop and validate SAS programs for identifying Non-Protocol Deviations.
10. Collaborate with Biostatistics and Data Management teams on clinical trials and projects.
11. Maintain and archive SAS programming documentation.
12. Assist in establishing and maintaining SOPs, documentation standards, and programming standards.
13. Stay informed on new SAS developments relevant to clinical data management and update the team accordingly.
14. Ensure KPIs and metrics for assigned studies are met.
15. Complete required trainings timely and accurately record time entries in the TRACK system.
16. Perform additional tasks as assigned.

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 their application to clinical trials.
• Proficiency in SAS and familiarity with CDISC standards (SDTM, ADaM).
• Strong planning and organizational skills.
• Team-oriented mindset.

What We Offer:

We provide a competitive salary, bonuses, and benefits, along with opportunities for professional growth 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 in conducting a wide range of clinical studies globally. We leverage advanced technology and innovative approaches to meet the complex demands of our projects, offering comprehensive services from trial start-up to data management and pharmacovigilance.