Especialista En Compras Internacionales Con Proyección Global

Kronospan; Burgos; Remote; EUR 65,000 - 95,000; Full time

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer to work remotely on a sponsor-dedicated program within a pharmaceutical client environment. You will independently manage data creation, reporting, and analysis activities, with autonomy and ownership in a fully embedded role.

Responsibilities include generating SDTM/ADaM specifications, developing SAS and R programs, and overseeing CRO statistical programming to ensure high-quality outputs across studies.

Qualifications

• Experience in clinical statistics programming for drug development.
• Strong knowledge of SAS programming and data derivation.
• Experience with SDTM/ADaM specifications and dataset creation.

Responsibilities

• Generate SDTM/ADaM specifications and datasets for multiple studies.
• Develop SAS programs to create datasets, listings, tables, and graphs.
• Deliver high-quality programming outputs and validate SAS and/or R code.
• Oversee CROs' statistical programming activities to ensure quality.

Skills

SAS

R

SDTM

ADaM

listing generation

Tools

define.xml

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.

• 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