Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must
Not Disclosed•Full-TimeHybrid
location_on110, South Grand Avenue West, Hawthorne Place, Springfield, Sangamon County, Illinois, 62704, United States
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 culture prizes innovation, seeking intelligent solutions using leading-edge technology, and we believe in collaboration by inviting a diversity of perspectives to create a wealth of possibilities.
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 and Late-stage clinical trials. This role is designed for individuals who value autonomy and ownership, empowering you to drive 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 handle data manipulation, analysis, and reporting for both safety and efficacy, while also creating complex ad-hoc reports and reviewing submission documents. This is an exciting opportunity to join 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 collaborate effectively within a globally dispersed team environment, working with cross-cultural partners to meet challenging timelines.
Hiring Process and Application
To be successful in this position, candidates should possess a strong background in SAS programming within the pharmaceutical and biotech industry, specifically with clinical endpoint data and pharmacokinetic data. We enable employee success through consistent training, development, and support. Please review the specific qualifications regarding education and years of experience to ensure you meet the requirements for this dedicated role.
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
110, South Grand Avenue West, Hawthorne Place, Springfield, Sangamon County, Illinois, 62704, United States
Springfield, Illinois
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 complex ad-hoc reports utilizing raw clinical trial data
- check_circleGenerate and validate statistical programming deliverables including SDTM, ADaM, and TFLs
- check_circleCommunicate with cross-functional teams and clients regarding project specifications and status
- check_circleCreate and review submission documents and eCRTs for regulatory filings
- check_circleProduce and perform QC/validation programming for clinical trial data
Requirements
- verifiedBachelor's degree in Statistics, Computer Science, Mathematics, or related field
- verified8+ years SAS programming in clinical trials with bachelor's degree (or 6+ years with master's)
- verifiedExperience with Early Development studies
- verifiedExpertise in clinical endpoint data (efficacy and safety) and pharmacokinetic data
- verifiedProficiency in CDISC SDTM and ADaM standards
- verifiedKnowledge of submission standards (Define.XML, SDRG, aCRF)
- verifiedExperience with Pinnacle 21 Enterprise
- verifiedPreferred: R, SPlus, NonMem
- verifiedPreferred: Oncology studies experience
Nice to Have
Experience with R, SPlus, or NonMem. Experience supporting Oncology studies.
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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 complex ad-hoc reports utilizing raw clinical trial data.
What are the requirements for this Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must role?expand_more
Cytel is looking for candidates who meet the following requirements: Bachelor's degree in Statistics, Computer Science, Mathematics, or related field; 8+ years SAS programming in clinical trials with bachelor's degree (or 6+ years with master's); Experience with Early Development studies; Expertise in clinical endpoint data (efficacy and 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 110, South Grand Avenue West, Hawthorne Place, Springfield, Sangamon County, Illinois, 62704, 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.