Auditor Senior De Finanzas Y Riesgos Internacionales

Kpmg España; Málaga; Remote; EUR 90,000 - 130,000; Full time

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer for a fully remote role within a sponsor-driven program. The role emphasizes autonomy, ownership, and delivering compliant SDTM/ADaM outputs across multiple studies.

You will develop SAS and R pipelines, oversee CRO deliverables, support regulatory submissions, and ensure alignment with FDA/EMA guidelines while collaborating with biostatistics and programming teams.

Qualifications

• Extensive experience in statistical programming for clinical development.
• Strong knowledge of SDTM/ADaM data structures and CSR support.
• Experience liaising with CROs and clinical vendors.
• Ability to work with minimal supervision on complex analyses.
• Familiarity with FDA/EMA regulations for submissions.

Responsibilities

• Generate SDTM, ADaM specifications, datasets, reviewer’s guides and define.xml files for multiple studies.
• Develop SAS programs to generate datasets, listings, tables and graphs.
• Deliver high-quality statistical programming results in SAS and/or R for development programs.
• Oversee CROs' programming deliverables to meet timelines.
• Support preparation of clinical study reports, regulatory submissions and publications.
• Understand and apply FDA regulations for reporting clinical trial data.
• Contribute to standards for programming tools, outputs, and macros.
• Participate in CRFs, edit check specs, and data validation plans.
• Provide review/author data transfer specs for external vendors.
• Collaborate with internal and external partners to meet project goals.
• Provide SOPs/work instructions related to statistical programming practices.

Skills

Statistical programming

Clinical trials

SAS programming

R programming

Leadership / CRO oversight

Tools

SAS

R

Job description

Senior/Principal Statistical Programmer SAS + R (Remote)

**Sponsor-dedicated:**
Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.
**Position Overview:**
This position reports to the Director, Biostatistics and Programming in the FSP Services business unit in Cytel. The Principal Statistical Programmer works independently with only concept level instruction and very little supervision, tracks progress, and provides expert technical support to team members. We are looking for a highly experienced senior statistical programmer who will work on clinical development programs on different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, high-quality manner. This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials.
**As a Principal Statistical Programmer, your responsibilities will include:**

• Generate SDTM, ADaM specifications, datasets, reviewer's guide and define.xml files for multiple studies
• Develop SAS programs which generate datasets, complex listings, tables (including those with descriptive and standard inferential statistics in collaboration with a Statistician), and complex graphs
• Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs tailored to clinical development programs' needs
• Participate in overseeing CRO's statistical programming deliverables for multiple clinical studies to ensure high-quality and meet the pre-specified timelines
• Support the preparation of clinical study reports, regulatory submissions, publications, annual DSUR, and exploratory analyses
• Understand and follow FDA regulations which affect the reporting of clinical trial data. This includes good clinical practice and guidelines for electronic submissions.
• Contribute to the creation, maintenance, documentation, and validation of standards for programming tools, outputs, and macros
• Participate in the development of CRFs, edit check specifications, and data validation plans
• Provide review and/or author data transfer specifications for external vendor data
• Collaborate with internal and external functions (e.g. CROs, software vendors, clinical development partners, etc.) to ensure meeting project timelines and goals
• Provide review and/or author SOPs and/or Work Instructions related to statistical programming practices

**Here at Cytel we want our employees to succeed