Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must
Not Disclosed•Full-TimeHybrid
location_onFranklin Street, Downtown, Providence, Providence County, Rhode Island, 02902, United States
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 the next generation of patient treatments. While you are dedicated to the client, you will have the full backing of Cytel behind you. This program offers a unique environment where individuals are empowered to work with autonomy and ownership, making it an exciting time to join.
Our values drive how we approach every challenge: we apply scientific rigor to reveal the full promise inherent in data, nurture intellectual curiosity, and encourage a desire for discovery. We believe in collaboration, inviting a diversity of perspectives to create a wealth of possibilities, and we prize innovation by seeking intelligent solutions using leading-edge technology.
In this hybrid role (based in PA or NJ), you will leverage advanced SAS programming skills and proficiency in CDISC standards to support or lead early or late-stage clinical trials. Your day-to-day will involve generating and validating statistical programming deliverables, including SDTM, ADaM, and TFLs, across all therapeutic areas. You will perform data manipulation, analysis, and reporting for both safety and efficacy, utilizing SAS to create complex ad-hoc reports from raw data.
You will also be responsible for production and QC/validation programming, creating and reviewing submission documents and eCRTs, and applying a strong understanding of efficacy analysis. As a team player, you will communicate with cross-functional teams and the client regarding project specifications, status, and inquiries. You will be expected to perform lead duties when called upon and remain adaptable and flexible as priorities shift.
Cytel is committed to employee success and enables this through consistent training, development, and support. To apply, please submit your resume highlighting your experience with clinical trial data, specifically in early development studies, pharmacokinetic data, and CDISC standards.
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 model: Hybrid
Franklin Street, Downtown, Providence, Providence County, Rhode Island, 02902, United States
Providence, Rhode Island
Experience with R, SPlus, or NonMem. Experience supporting Oncology studies.
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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).