- Cytel (Harrisburg, PA)
- …& R-Shiny. + At least 5 years of R/ SAS programming experience with clinical trial data . + General knowledge of regulatory requirements and drug development ... programmer will also be required to utilize the SAS software system; they should be proficient in ...support electronic regulatory submissions; providing systems and support for clinical data management staff, clinical … more
- Cytel (Harrisburg, PA)
- …Performing data manipulation, analysis and reporting of clinical trial data , both safety and efficacy (ISS/ISE), utilizing SAS programming + Production ... this new program. **Position Overview:** As a Senior Statistical Programmer , you will leverage your advanced SAS ...8 years of SAS programming working with clinical trial data in the Pharmaceutical &… more
- Merck (North Wales, PA)
- …Specific Required Skills and Experience:** + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS /MACRO, ... Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial...understanding of statistical terminology and concepts. + Familiarity with clinical data management concepts + Experience in… more
- Cytel (Harrisburg, PA)
- …Clinical Development, and other functional representatives to develop, maintain and document clinical data standards. This role also acts as a statistical ... + Provides technical and/or operational guidance in the application of industry clinical data standards within the statistical programming data … more
- Teva Pharmaceuticals (West Chester, PA)
- …of experience in a pharmaceutical or clinical research setting as a programmer . **Compensation Data ** The annual starting salary for this position is between ... and new people to make a difference with. **The opportunity** The clinical programming department provides SAS programming support; develops and generates… more
- Organon & Co. (Plymouth Meeting, PA)
- …Write or review and approve data specifications for SDTM and ADaM. + Write SAS programs to generate or validate SDTM, ADaM, and TLFs. + Manage and willingness to ... + Support and manage statistical programming activities to all clinical development programs and internal initiatives. + Act as...and internal initiatives. + Act as a lead statistical programmer and project manager for the studies, compound and… more