Senior Statistical Programmer – FSP

Clinical Outcomes Solutions

Senior Statistical Programmer at Cytel leveraging SAS skills for global pharmaceutical clients. Supporting Phase I-IV clinical trials with a focus on oncology and efficacy analysis.

Posted 7/23/2026full-timeRemote • 🇨🇴 ColombiaSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support clinical trials, with a strong focus on data manipulation, analysis, and reporting. Capable of generating and validating datasets and submission documents while effectively collaborating with cross-functional teams.

Highest-signal resume keywords

Advanced SAS ProgrammingCDISC SDTM / ADaM StandardsData Manipulation and AnalysisQC / Validation SkillsEfficacy Analysis

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

SAS ProgrammingData ManipulationClinical Trial Data AnalysisEfficacy AnalysisQC / Validation ProgrammingAd-Hoc ReportingSDTM DatasetsADaM DatasetsSubmission DocumentsDefine.xml

Soft Skills

Analytical SkillsTroubleshooting SkillsTeam PlayerAdaptabilityFlexibility

Industry Keywords

Pharmaceutical IndustryBiotech IndustryClinical TrialsOncology StudiesImmunology StudiesDrug Development Life Cycle

About the role

Key responsibilities & impact

Leverage advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials.
Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming
Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)
Production and QC / validation programming
Generating complex ad-hoc reports utilizing raw data
Applying strong understanding/experience of Efficacy analysis
Creating and reviewing submission documents and eCRTs
Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries
Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
Being adaptable and flexible when priorities change

Requirements

What you’ll need

Bachelor’s degree in one of the following fields Statistics, Computer Science, Mathematics, etc.
At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or equivalent. At least 6 years of related experience with a master’s degree or above.
Study lead experience, preferably juggling multiple projects simultaneously preferred.
Strong SAS data manipulation, analysis and reporting skills.
Solid experience implementing the latest CDISC SDTM / ADaM standards.
Strong QC / validation skills.
Good ad-hoc reporting skills.
Proficiency in Efficacy analysis.
Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data.
Submissions experience utilizing define.xml and other submission documents.
Experience supporting oncology or immunology studies would be a plus.
Excellent analytical & troubleshooting skills.
Ability to provide quality output and deliverables, in adherence with challenging timelines.
Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

Benefits

Comp & perks

Consistent training, development and support.