Your key responsibilities:
Your responsibilities include, but not limited to:

• Contribute to statistical programming activities as Statistical Programmer for phase I to IV clinical studies or project level activities.

• Build and maintain effective working relationship with cross-functional team. Contribute to assigned parts of process improvement, standardization and other non-clinical initiatives.

• Review the eCRF, data structures and data review activities. Comply with company, department and industry standards (e.g. CDISC) and processes, create / support the review of programming specifications as part of the analysis plans.

• Ensure timely and quality development and validation of datasets and outputs (datasets, tables, figures and listings) for study-documents according to specifications.

• Responsible for quality control and audit readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis results.

• Maintain up-to-date knowledge of programming software (e.g. SAS) as well as industry requirements (e.g. CDISC SDTM/ADaM, eCTD, Define.xml), attend functional meetings and trainings.

• Under minimal guidance participates in establishing successful working relationship on individual studies with external associates according to agreed contract and internal business guidance.

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Minimum requirements

What you’ll bring to the role:

• BE/BS/MS or international equivalent experience in statistics, computer science, mathematics, life sciences or related field with Ideally 2+ years of work experience in a programming role preferably supporting clinical trials.
• Basic SAS experience within a Statistical Programming environment to develop and validate deliverables.
• Basic experience in contributing to statistical analysis plans and/or constructing technical programming specifications.
• Basic understanding of regulatory requirements relevant to Statistical Programming (e.g. GCP).
• Good communications and negotiation skills, ability to work well with others globally.