Sr. Manager, Biostatistics

Alfasigma; Oña; A distancia; EUR 65.000 - 100.000; Jornada completa

Descripción de la vacante

Cytel seeks a Senior/Principal Statistical Programmer (SAS + R) for a fully remote role, embedded with a global pharmaceutical client. You will drive programming initiatives, ensure high-quality data outputs, and oversee CRO deliverables with autonomy.

You will generate SDTM/ADaM specifications, develop SAS programs for datasets, listings, and tables/graphs, and collaborate with statisticians and senior staff to meet project timelines.

Formación

• Senior statistical programming experience in clinical trials.
• Experience with SDTM/ADaM specifications and define.xml.
• Ability to oversee CRO programming deliverables and timelines.

Responsabilidades

• Generate SDTM, ADaM specifications, datasets, reviewer's guide and define.xml files for multiple studies.
• Develop SAS programs which generate datasets, listings, tables and graphs.
• Deliver high-quality SAS and/or R programs tailored to clinical development needs.
• Oversee CRO's statistical programming deliverables to ensure quality and timelines.
• Provide ongoing technical support to the team.

Conocimientos

SAS

R

Clinical programming

SDTM/ADaM

Herramientas

SAS

R

Descripción del empleo

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