Sr. Manager, Biostatistics

Alfasigma; España; Remote; EUR 65,000 - 90,000; Full time

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer to work remotely with a major pharmaceutical client. You will be responsible for delivering SDTM/ADaM specifications and complex statistical programming across studies, using SAS and R, with minimal supervision.

You will oversee CRO programmers and ensure high-quality data deliverables while collaborating with the Biostatistics team in a sponsor-dedicated setup.

Qualifications

• Experience in clinical trials programming with SAS and/or R.
• Ability to develop SDTM/ADaM specifications and reporting tools.
• Strong communication skills for collaboration with statisticians and CROs.

Responsibilities

• Generate SDTM/ADaM specs, datasets, and define.xmls for multiple studies.
• Develop SAS programs to produce listings, tables, and graphs.
• Deliver high-quality statistical programming outputs and oversee CRO programmers.

Skills

SAS

R

Clinical Trials

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