Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must
Not Disclosed•Full-TimeHybrid
location_on328, West Ardenwood Drive, Ardenwood, Mid City, Baton Rouge, East Baton Rouge Parish, Louisiana, 70806, 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 have the autonomy and ownership to drive the next generation of patient treatment, backed by the full support of Cytel.
This is an exciting opportunity to join a new program where you can leverage advanced SAS programming skills and CDISC standards (SDTM & ADaM) to reveal the full promise inherent in data. The role is hybrid and office-based in Pennsylvania (preferred) or New Jersey.
Our Values
At Cytel, we believe in applying scientific rigor to data and nurturing intellectual curiosity. We encourage everyone to approach new challenges with enthusiasm and a desire for discovery. We prize collaboration, inviting a diversity of perspectives to create a wealth of possibilities, and we seek intelligent solutions using leading-edge technology.
Hiring Process
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. Cytel Inc. is an Equal Employment / Affirmative Action Employer.
Work location
Work model: Hybrid
328, West Ardenwood Drive, Ardenwood, Mid City, Baton Rouge, East Baton Rouge Parish, Louisiana, 70806, United States
Baton Rouge, Louisiana
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
Similar Job Opportunities
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
In this Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must at Cytel role, you 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
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, etc.; 8+ years SAS programming with clinical trial data (Pharma/Biotech) with Bachelor's; 6+ years related experience with Master's degree or above; Experience with Early Development studies; Expertise in clinical endpoint data (efficacy/safety) and pharmacokinetic data; and Proficiency in CDISC SDTM and ADaM standards.