Junior Statistical SAS Programmer

Opis S.r.l.; Lucca; In loco; EUR 30.000 - 50.000; Tempo pieno

Descrizione del lavoro

An international clinical research organization in Tuscany is seeking a Junior Statistical SAS Programmer to develop SAS programs for clinical studies. The ideal candidate will have experience in pharmaceutical research and proficiency in SAS and CDISC standards. This role offers competitive salary, bonuses, and opportunities for professional growth.

Servizi

Competitive salary

Bonuses

Benefits

Opportunities for professional growth

Competenze

• Minimum 1 year of experience in CRO, biotech, pharma, or research institutes in a similar role.
• Knowledge of HA requirements related to pharmaceutical research and SAS programming.
• Understanding of statistics and its applications in clinical trials.

Mansioni

• Develop SAS programs for generating datasets, tables, figures, and listings.
• Utilize CDISC guidelines to generate SDTM / ADaM datasets.
• Collaborate with Biostatistics and Data Management staff on clinical trials/projects.

Conoscenze

SAS programming

CDISC standards

Statistical analysis

Teamwork

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 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.

Key Responsibilities:

• Develop SAS programs for generating datasets, tables, figures, and listings for clinical trials, publications, and Health Authorities requests
• Utilize CDISC guidelines to generate SDTM / ADaM datasets
• Write programming specifications for analysis datasets
• Validate ADaM datasets using Pinnacle 21
• Prepare, maintain, and archive CDISC documentation for ADaM (Define.xml and ADRG)
• Contribute to developing standard SAS macros and validation documents
• Liaise with Data Management team to develop SAS programs/macros/utilities to detect data discrepancies
• Handle external clinical data, develop SAS programs to import/reconcile data
• Develop and validate SAS programs for identifying Non-Protocol Deviations
• Collaborate with Biostatistics and Data Management staff on clinical trials/projects
• Maintain and archive SAS programming documentation
• Assist in establishing and maintaining SOPs and related documentation
• Stay informed on new SAS developments relevant to clinical data management
• Ensure KPIs and metrics are met for assigned studies
• Complete required trainings timely
• Maintain accurate daily entries in the TRACK system
• Perform additional tasks as assigned

Qualifications:

• Minimum 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
• Understanding of statistics and its applications in clinical trials
• Proficiency in SAS and CDISC standards (SDTM, ADaM)
• Strong planning and organizational skills
• Team-oriented mindset

What We Offer:

A competitive salary, bonuses, and benefits, along with opportunities for professional growth within an expanding international company.

Please review the personal data processing notice on our website.

Who We Are:

OPIS is an international CRO with 25 years of experience in conducting various clinical studies globally. We provide state-of-the-art technology solutions and innovative approaches to complex projects, covering all phases of drug trials and offering comprehensive clinical research services.

I accept the Candidate Privacy Policy and authorize processing of my personal data contained in my CV.