Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must
Not Disclosed•Full-TimeHybrid
location_on6317, West Markham Street, Little Rock, Big Rock Township, Pulaski County, Arkansas, 72205, United States
About the Role
This position is sponsor-dedicated, placing you fully embedded within one of our global pharmaceutical clients. As a Senior Statistical Programmer, you will be at the heart of their innovation, supporting or leading Early and Late-stage clinical trials. You will work with autonomy and ownership, empowered to drive the next generation of patient treatment, with the full support of Cytel behind you.
This is an exciting time to join a new program designed to reveal the full promise inherent in data. You will apply scientific rigor to clinical trial data, utilizing advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to generate and validate statistical programming deliverables. The role spans all therapeutic areas, including Early Development Statistics and PK/PD Modeling and Simulation, requiring you to handle complex data manipulation, analysis, and reporting for both safety and efficacy.
Our Values
At Cytel, we nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and a desire for discovery. We believe in collaboration, inviting a diversity of perspectives to create a wealth of possibilities. We prize innovation and seek intelligent solutions using leading-edge technology.
Location and Work Model
This role is hybrid and office-based, with a preference for locations in Pennsylvania (PA) or New Jersey (NJ).
Hiring Process
To be successful in this position, candidates must demonstrate a strong background in clinical trial data within the Pharmaceutical and Biotech industry. We look for individuals with a Bachelor's degree in Statistics, Computer Science, Mathematics, or a related field, along with significant experience in SAS programming and CDISC standards. Specific expertise in Early Development studies, clinical endpoint data, and pharmacokinetic data is essential.
Equal Opportunity
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
6317, West Markham Street, Little Rock, Big Rock Township, Pulaski County, Arkansas, 72205, United States
Little Rock, Arkansas
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, etc.
- verified8+ years SAS programming with clinical trial data (Pharma/Biotech) with Bachelor's 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 SAS data manipulation, analysis, and reporting skills
- verifiedStrong QC and validation skills
- verifiedAbility to work in a globally dispersed team
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 (preferred for 6 years experience).
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
A Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must at Cytel is responsible for the following: 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
Cytel is looking for candidates who meet the following requirements: Bachelor's degree in Statistics, Computer Science, Mathematics, etc.; 8+ years SAS programming with clinical trial data (Pharma/Biotech) with Bachelor's 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 6317, West Markham Street, Little Rock, Big Rock Township, Pulaski County, Arkansas, 72205, 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 (preferred for 6 years experience).
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.