Senior Migration Consultant - Clinical Data Programming

Veeva Systems; Gijón; Remote; EUR 70,000 - 100,000; Full time

Job summary

Cytel seeks a Senior/Principal Statistical Programmer SAS + R (Remote) to support a pharmaceutical client. You will work with autonomy on programming tasks across programs and deliver high-quality outputs with minimal supervision.

Responsibilities include generating SDTM/ADaM specs, datasets, listings, tables and graphs, delivering reporting solutions, and overseeing CROs to meet timelines. You will report to the Director of Biostatistics and Programming in the FSP Services unit.

Qualifications

• Extensive SAS programming experience for clinical development programs.
• Strong knowledge of statistical programming for SDTM/ADaM.
• Experience delivering complex tables, listings, and figures with statistics.

Responsibilities

• Generate SDTM, ADaM specifications, datasets, reviewer's guide and define.xml files for multiple studies.
• Develop SAS programs to create datasets, listings, tables, and graphs with descriptive and inferential statistics.
• Deliver high-quality SAS and/or R programs tailored to clinical development needs.
• Oversee CROs' statistical programming deliverables to meet timelines.
• Provide expert technical support to the team.

Skills

SAS

R

Statistical programming

Clinical trials

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