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  5. Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must
Cytel logo

Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must

Not Disclosed•Full-TimeHybrid

location_onMeredith Corporation, 1716, Locust Street, Meredith Corporation, Des Moines, Polk County, Iowa, 50309, United States

Apply Now

About the Team and Mission

Cytel is dedicated to applying scientific rigor to reveal the full promise inherent in data. We nurture intellectual curiosity, encouraging our team to approach new challenges with enthusiasm and a desire for discovery. Our values center on collaboration, inviting a diversity of perspectives to create a wealth of possibilities, and we prize innovation by seeking intelligent solutions using leading-edge technology.

About the Role

This is a sponsor-dedicated position where you will work fully embedded within one of our global pharmaceutical clients. As a Senior Statistical Programmer, you will be at the heart of the client's innovation, supporting or leading Early or Late-stage clinical trials. This role is designed for individuals who are empowered to work with autonomy and ownership while driving the next generation of patient treatment.

You will leverage advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to generate and validate statistical programming deliverables. Your work will span all therapeutic areas, including Early Development Statistics and PK/PD Modeling and Simulation. You will perform data manipulation, analysis, and reporting of clinical trial data (both safety and efficacy), create complex ad-hoc reports, and assist in preparing submission documents. This is an exciting opportunity to contribute to a new program during a pivotal time for the industry.

Work Environment

This position is hybrid and office-based, with a preference for locations in Pennsylvania (PA) or New Jersey (NJ). You will work within a globally dispersed team environment, collaborating with cross-cultural partners and internal cross-functional teams to manage project specifications, status, and inquiries.

Hiring Process and Support

Cytel is committed to employee success and enables this through consistent training, development, and support. We look for candidates who are adaptable, flexible when priorities change, and willing to go the extra distance to meet deadlines. While specific interview steps are not detailed here, the role requires strong analytical and troubleshooting skills to deliver quality output under challenging timelines.

Equal Opportunity Statement

Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.

Work location

Work model: Hybrid

location_on

Meredith Corporation, 1716, Locust Street, Meredith Corporation, Des Moines, Polk County, Iowa, 50309, United States

Des Moines, Iowa

Key Responsibilities

  • check_circlePerform data manipulation, analysis, and reporting of clinical trial safety and efficacy data using SAS
  • check_circleDevelop and validate global programming standards for ADaM datasets and efficacy analysis
  • check_circleDesign and develop complex programming algorithms for clinical endpoint and pharmacokinetic data
  • check_circleGenerate and validate statistical programming deliverables including SDTM, ADaM, and TFLs
  • check_circleCreate and review submission documents and eCRTs for regulatory filings
  • check_circleProduce complex ad-hoc reports utilizing raw data to support project needs
  • check_circleCollaborate with cross-functional teams and clients to address project specifications and status updates

Requirements

  • verifiedBachelor's degree in Statistics, Computer Science, Mathematics, or related field
  • verified8+ years SAS programming in pharmaceutical/biotech with bachelor's degree (or 6+ years with master's)
  • verifiedExperience with Early Development studies
  • verifiedExpertise in clinical endpoint data (efficacy/safety) and pharmacokinetic data
  • verifiedProficiency in CDISC SDTM and ADaM standards
  • verifiedKnowledge of submission standards (Define.XML, SDRG, aCRF)
  • verifiedExperience with Pinnacle 21 Enterprise
  • verifiedStrong QC and validation skills
  • verifiedAbility to work in hybrid office location (PA or NJ)

Nice to Have

Experience with R, SPlus, or NonMem. Experience supporting Oncology studies.

Cytel logo
Company

Cytel

Industry

scientific & qa

View company profilearrow_forwardlanguageWebsite
Quick Overview

Experience

8+ yrs (Senior)

Education

Bachelor's degree in Statistics, Computer Science, Mathematics, etc.

Job Type

Full-Time

Skills Required

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Skills, education and keywords

Skills: Sas, Cdisc, SDTM, Adam, PK/PD Modeling And Simulation, Efficacy Analysis, Safety Analysis, R, Splus, Nonmem.

Education: Bachelor's degree in Statistics, Computer Science, Mathematics, etc.; Master's degree or above (reduces experience requirement to 6 years).

Frequently asked questions about Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must at Cytel

What does a Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must at Cytel do?expand_more
Day-to-day, the Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must at Cytel will perform data manipulation, analysis, and reporting of clinical trial safety and efficacy data using sas; develop and validate global programming standards for adam datasets and efficacy analysis; design and develop complex programming algorithms for clinical endpoint and pharmacokinetic data; and generate and validate statistical programming deliverables including sdtm, adam, and tfls.
What are the requirements for this Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must role?expand_more
To qualify for the Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must at Cytel position, applicants should have: Bachelor's degree in Statistics, Computer Science, Mathematics, or related field; 8+ years SAS programming in pharmaceutical/biotech with bachelor's degree (or 6+ years with master's); Experience with Early Development studies; Expertise in clinical endpoint data (efficacy/safety) and pharmacokinetic data; Proficiency in CDISC SDTM and ADaM standards; and Knowledge of submission standards (Define.XML, SDRG, aCRF).
Where is the Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must role at Cytel located?expand_more
Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must at Cytel is based in Meredith Corporation, 1716, Locust Street, Meredith Corporation, Des Moines, Polk County, Iowa, 50309, United States. This is a hybrid role.
Is this Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must job remote, hybrid, or on-site?expand_more
Cytel has listed this Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must role as hybrid.
How much experience is required for this Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must role?expand_more
Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must at Cytel typically requires 8+ years of relevant experience at the senior level.
What skills do you need for the Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must role at Cytel?expand_more
Key skills for Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must at Cytel include Sas; Cdisc; SDTM; Adam; PK/PD Modeling And Simulation; Efficacy Analysis; Safety Analysis; and R.
What education is required for Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must at Cytel?expand_more
Educational requirements for this role: Bachelor's degree in Statistics, Computer Science, Mathematics, etc.; and Master's degree or above (reduces experience requirement to 6 years).
What category does the Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must role belong to?expand_more
Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must at Cytel is part of the scientific & qa job category on Recrutus.
Recrutus

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Search roles by city, category, skill, or job type — explore verified US employers, salary benchmarks, and remote-friendly teams hiring nationwide.

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Jobs in TexasJobs in CaliforniaJobs in New YorkJobs in FloridaJobs in North CarolinaJobs in OhioAll states →
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Healthcare & Nursing jobsLogistics & Warehouse jobsEngineering jobsIT jobsSales jobsHospitality & Catering jobsAccounting & Finance jobs
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About usFAQContactPrivacy policyUS privacy notice

Recrutus helps candidates discover roles that match their skills and helps teams reach qualified applicants faster. Browse by metro, discipline, or work style — from internships to senior leadership.

© 2026 Recrutus. All rights reserved.
Terms of serviceCookie policyAcceptable useDMCA policyEmployer termsCandidate terms
SasCdiscSDTMAdamPK/PD Modeling And SimulationEfficacy AnalysisSafety AnalysisRSplusNonmem
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