Senior Statistical Programmer, FSP

Clinical Outcomes Solutions

Senior Statistical Programmer working on Phase I-IV clinical trials in collaboration with global pharmaceutical clients. Leading data analysis and contributing to significant clinical developments using SAS.

Posted 6/9/2026full-timeRemote • 🇮🇳 IndiaSeniorWebsite

About the role

Key responsibilities & impact

Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), 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
Performing lead duties when called upon
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 immunology, respiratory or oncology 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

Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support.

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

SAS programmingdata manipulationdata analysisreportingSDTMADaMQCvalidationad-hoc reportingEfficacy analysis

Soft Skills

communicationteam playeradaptabilityflexibilityanalytical skillstroubleshootingtime managementleadershipcross-functional collaborationproblem-solving