- Regeneron Pharmaceuticals (Warren, NJ)
- A principal statistical programmer provides timely support to the study team on all programming matters according to the project strategies. As an integral part of a ... provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis… more
- AbbVie (Florham Park, NJ)
- …report clinical trial data under direction of Senior Statistical Analyst. + Provide SAS programming support for clinical trials. + Develop SAS programs ... of work experience in each of the following: + providing SAS programming support for pharmaceutical industry clinical trials; + coding SAS programs using … more
- Merck (Rahway, NJ)
- …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial environment + MS in ... Life Sciences, Engineering or related field plus 3 years SAS programming experience in a clinical trial...3 years SAS programming experience in a clinical trial environment _Department Required Skills and Experience:_ +… more
- Johns Hopkins University (Baltimore, MD)
- …ACASI and/or Qualtrics. + Familiarity with a statistical analysis program (STATA, SAS or R preferred). Classified Title: Programmer Analyst Role/Level/Range: ... and update databases-provide programming for projects with continued ongoing support. + Manage clinical and other types of data sets and conduct data cleaning and… more
- 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 5-9 years SAS programming experience in a clinical trial environment + MS in ... Applied Mathematics, Life Sciences, Engineering or related field plus 3-7 years SAS programming experience in a clinical trial environment **Department Required… more
- BeOne Medicines (San Mateo, CA)
- …industries or academic research. Experience with oncology trials.** **Expert level SAS programmer with experience in delivering complex programming assignments ... scientific subject, or equivalent related experience** **Experience:** **Minimum 7+ years' clinical research and development programming experience using SAS **… more
- Teva Pharmaceuticals (West Chester, PA)
- …Required: Bachelors + 7 year, Masters + 6 years in a pharmaceutical or clinical research setting as a programmer . Experience Preferred: Specialized or Technical ... for managing the timely and accurate execution of programming components of clinical trials and supports the development, regulatory approval and market acceptance… more
- IQVIA (Durham, NC)
- …to development of protocols, analysis plans, PK/PD analysis, and pharmacometric reports for pre- clinical or Phase I-IV clinical studies. + Consult with ... Clinical Pharmacology staff on study design, analyses, clinical development plans. + Plan and execute a wide range of pharmacometric analyses to inform … more
- Ascendis Pharma (Palo Alto, CA)
- …at least 7 years of relevant experience. + Proven experience as a lead programmer for clinical trials and complex technical projects. + Excellent knowledge of ... will be expected to provide timely and strategic programming support to clinical study teams in alignment with project goals. This role combines hands-on… more