- Merck (Rahway, NJ)
- …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial environment. + MS in ... Engineering or related field plus 7 or more years SAS programming experience in a clinical trial...more years SAS programming experience in a clinical trial environment. **Department Required Skills and Experience:** +… more
- Merck (Rahway, NJ)
- …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 3 years SAS programming experience in a clinical trial environment OR a ... Life Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial...5 years SAS programming experience in a clinical trial environment. **Minimum requirement:** + Must have experience… more
- Cytel (Trenton, NJ)
- …following fields Statistics, Computer Science, Mathematics, etc. + At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & ... a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM...or lead one or more Early or Late stage clinical trials. **This role is Hybrid office based in… more
- Astrix Technology (NJ)
- … Project Manager + Site Start Up Specialists + Clinical Data Manager + Clinical Development Associates + SAS Programmer + and more! We are an equal ... ** Clinical Operations Professionals** Clinical Remote, NJ, US Pay Rate Low: 25 | Pay Rate High: 80 + Added - 06/02/2025 Apply for Job Astrix has been partnered… more
- Merck (Rahway, NJ)
- …Mathematics, Life Sciences, Engineering or related field plus at least 2 years SAS programming experience in a clinical trial environment. **Required Experience ... the guidance of a senior-level programmer supporting early-phase oncology clinical trials. Collaborate with other programming colleagues and biostatisticians and/or… more
- Merck (Rahway, NJ)
- …Mathematics, Life Sciences, Engineering or related field plus at least 2 years SAS programming experience in a clinical trial environment. **Required experience ... inclusion in study reports and regulatory submissions. + Produce SAS transport files and associated documentation for regulatory submissions....and skills** + Must possess SAS programming skills including data steps, procedures, SAS… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …programming related topics. **This role may be for you if have:** + Advanced SAS programming skills in a clinical data environment with expertise in at ... leadership and contributes to the programming support for processing data from clinical studies. Project requirements will be identified according to a Statistical… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …regulatory submission requirements. **This role may be for you if have:** + Advanced SAS programming skills in a clinical data environment with expertise in at ... leadership and contributes to the programming support for processing data from clinical studies. Project requirements will be identified according to a Statistical… more
- Bristol Myers Squibb (Princeton, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . Director, Clinical Pharmacology and Pharmacometrics The Director is responsible for ensuring ... clinical pharmacology support for a portfolio of assigned oncology...Programming experience is required (eg, NONMEM, R, and WinNonlin. SAS , Splus, etc.) + Quantitative data analysis, POP PK/PD,… more
- AbbVie (Jersey City, NJ)
- …with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Clinical Operations. Responsibilities: + Leads the statistical programming activities for ... the projects. + Develops and oversees the development of SAS programs for the creation of ADaM data sets...CDISC standards. + Develops and oversees the development of SAS programs for the creation of Tables, Listings and… more