Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must
Not Disclosed•Full-TimeHybrid
location_on101, East Main Street, Monroe Ward, Richmond, Virginia, 23284, United States
About the Role
This position is sponsor-dedicated, meaning you will work 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 join a company driving the next generation of patient treatment, where you are empowered to work with autonomy and ownership.
This is an exciting time to join a new program designed to support your growth. 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, ensuring scientific rigor reveals the full promise inherent in data.
Our Culture
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. We are committed to your success through consistent training, development, and support.
Location
This role is hybrid and office-based, preferably in Pennsylvania (PA) or New Jersey (NJ).
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
101, East Main Street, Monroe Ward, Richmond, Virginia, 23284, United States
Richmond, Virginia
Key Responsibilities
- check_circlePerform data manipulation, analysis, and reporting of clinical trial safety and efficacy data using SAS
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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, 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).