- Merck (North Wales, PA)
- …all our company therapeutic areas except oncology. The senior statistical programmer will gather and interpret user requirements for programming requests, retrieve ... listings and figures according to statistical/modeling analysis plan. The senior programmer will be a key collaborator with statisticians, modelers, and colleagues… more
- Merck (North Wales, PA)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.… more
- Merck (North Wales, PA)
- …This position supports statistical programming activities for late-stage drug/vaccine clinical development projects. This may include leadership of one or ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.… more
- Teva Pharmaceuticals (West Chester, PA)
- …is required. + A minimum of 10 years of experience in a pharmaceutical or clinical research setting as a programmer . + Expert knowledge of the drug development ... enable high-quality, efficient, and compliant outputs for regulatory submissions and clinical trial reporting. + Lead and develop global programming teams, including… more
- Teva Pharmaceuticals (West Chester, PA)
- …+ A minimum of 8 years of professional experience in a pharmaceutical or clinical research setting as a programmer including supporting regulatory submissions is ... tools and dashboards and exploratory analytics to provide insights into our clinical trial data and to support decision-making across clinical development… more
- Geisinger (Danville, PA)
- …+ Possesses the critical thinking skills needed to provide statistical support to clinical investigators. + Experienced SAS or R programmer for both data ... doctorate-level biostatistician. Responsibilities include collaborating on the design of clinical research studies, writing biostatistical analysis plans for research… more
- Merck (North Wales, PA)
- …modeling and simulation stakeholders spanning all therapeutic areas. The senior programmer will gather and interpret user requirements, retrieve the required data, ... and figures according to the modeling analysis plans. The programmer will take on a data stewardship leadership role...field plus 5-9 years SAS programming experience in a clinical trial environment + MS in Computer Science, Statistics,… more