Senior Statistical Programmer - Remote (SAS + R, CDISC)

Toloka

Las Palmas de Gran Canaria

Remote

EUR 70,000 - 110,000

Full time

2 days ago

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Job summary

Cytel is seeking a Senior/Principal Statistical Programmer for remote work with a global pharmaceutical client. You will lead SAS programming tasks, ensure SDTM/ADaM compliance, and generate TLFs while collaborating across cross-functional teams to meet project timelines.

Ideal candidates have 8+ years of SAS experience in pharma/biotech, strong CDISC knowledge, and prior study lead or leadership experience.

Qualifications

Bachelor's degree in Statistics, Computer Science, Mathematics, or equivalent.
At least 8 years of SAS programming with clinical trial data.
Experience with CDISC SDTM/ADaM standards and submission documents.
Study lead experience preferred; ability to manage multiple projects.
Strong data manipulation, analysis and reporting skills.
Experience generating submissions documents (define.xml, etc.).

Responsibilities

Perform data manipulation, analysis and reporting of clinical trial data (safety and efficacy).
Generate and validate SDTM/ADaM datasets and TLFs.
Perform production and QC/validation programming.
Create complex ad-hoc reports from raw data.
Apply strong efficacy analysis understanding and techniques.
Contribute to submission documents and eCRTs; respond to client requests.
Lead when required and collaborate with global cross-functional teams.