- Merck & Co. (North Wales, PA)
- …or related field plus 12 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics, Applied Mathematics, Life ... field plus 10 or more years SAS programming experience in a clinical trial environment. Department Required Skills and Experience: Excellent interpersonal… more
- Merck & Co. (North Wales, PA)
- … statistical analysis and high-quality data to assist decision making in clinical trials .-This position supports statistical programming activities for ... datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing… more
- Merck & Co. (North Wales, PA)
- …datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing ... of patients and global human health. This position supports statistical programming activities for late stage drug/vaccine clinical...at least 5 years SAS programming experience in a clinical trial environment orMS in Computer Science,… more
- Merck & Co. (North Wales, PA)
- …or related field plus 5 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics, Applied Mathematics, Life ... or related field plus 3 years SAS programming experience in a clinical trial environment.Department Required Skills and Experience: Effective interpersonal… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …10 or More Years proven experience within pharmaceutical industry, or CROs supporting statistical analysis of clinical trials programming preferred- 7 or ... effective implementation of SDTM, ADaM and TLFs standard in clinical trial data analysis- Develop and maintain...Years proven experience within pharmaceutical industry, or CROs supporting statistical analysis of clinical trials … more
- WCG Clinical (Princeton, NJ)
- Principal Statistical Programmer (Remote) **General Information** **Location:** Princeton, NJ, Remote **Organization:** Statistics Collaborative **Job Type:** ... growth, foster compliance, and maximize efficiency for those performing clinical trials . WCG is proud to serve...to $152,000 GPS level: P4 **JOB SUMMARY:** A Principal Statistical Programmer will (a) mentor and oversee… more
- IQVIA (Los Angeles, CA)
- …therapeutic areas. We are seeking a highly skilled and motivated Principal Statistical Programmer with expertise in pharmacokinetics (PK) and pharmacodynamics ... our dynamic FSP team. Position Overview: As a Principal Statistical Programmer with a specialized focus on...pivotal role in the design, execution, and analysis of clinical trials to support the development of… more
- Merck (North Wales, PA)
- … statistical analysis and high-quality data to assist decision making in clinical trials . This position supports statistical programming activities for ... listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions...field plus 9 years SAS programming experience in a clinical trial environment. + MS in Computer… more
- Actalent (San Diego, CA)
- …of technical infrastructure to expedite conduct and evaluation of clinical trials and basic research. Performs statistical analysis and develops tracking ... systems to determine the efficiency of clinical trials . Evaluates databases and ...of a project team. Skills: Clinical research, Statistical programming, Clinical trial Additional… more
- Merck (North Wales, PA)
- …datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing ... field plus 9 years SAS programming experience in a clinical trial environment. MS in Computer Science,...may describe methodology to be programmed, an understanding of statistical terminology and concepts. + Familiarity with clinical… more
- Merck (Rahway, NJ)
- …Engineering or related field plus 12 years SAS programming experience in a clinical trial environment. MS in Computer Science, Statistics, Applied Mathematics, ... related field plus 10 or more years SAS programming experience in a clinical trial environment. **Department Required Skills and Experience:** + Excellent… more
- IQVIA (Austin, TX)
- …analysis for complex project or client requirements. **Job Details:** + Position: - Principal Statistical Programmer + Home Based + Min 4+ years of CRO/Pharma ... components and theory. + Excellent application development skills. + Strong understanding of clinical trial data and extremely hands on in data manipulations,… more
- Takeda Pharmaceuticals (Lexington, MA)
- …analysis datasets, dataset specifications, statistical tables, figures, and listings for clinical trials ; create standard macros that can be adapted to ... Takeda Development Center Americas, Inc. is seeking a Manager, Statistical Programmer in Lexington, MA with the...study level programming and oversight activities for analysis of clinical trial data, ensuring quality and timeliness;… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …+ Good knowledge of pharmaceutical clinical development (ie, understanding of statistical concepts, techniques, and clinical trial principles). Knowledge ... The Principal Statistical Programmer will lead and support...with 5+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical… more
- IQVIA (Durham, NC)
- …Pharma company. We are now expanding this team by adding a Principal/Lead level Statistical Programmer . Expect to be dedicated to this sponsor, working within ... in support of ISS/ISE + Communicate an understanding of statistical programming concepts, basic clinical principles and...+ 9 years or more in SAS programming for clinical trial data, working within a CRO… more
- IQVIA (Durham, NC)
- Senior or Principal Statistical Programmer **Why DSSS?** Data Sciences Staffing Solutions, DSSS or DS3, is a unit within IQVIA that provides our sponsors with ... tables, figures, and listings to support the analysis of clinical trials data. + Reviews output across...techniques such as macro language, advanced data manipulation, and statistical procedures. + Implements data management plans designed to… more
- Ascendis Pharma (Palo Alto, CA)
- …reports/visualizations to support clinical data review and process efficiency. The Clinical Programmer will lead clinical programming activities across ... for employees to grow and develop their skills. The Clinical Data Programmer will be responsible for...BASE/SAS, SAS/STAT, SAS MACROS + Strong knowledge of Oncology clinical trials + Data Visualization tools (like… more
- Harvard University (Cambridge, MA)
- …on research and teaching. Our 70+ faculty are leaders in the development of statistical methods for clinical trials and observational studies, studies on ... an office setting Position Description: We are seeking a Programmer /Data Scientist to join our dynamic team. Duties and...SQL + Function as a resource for the Senior Programmer , to help debug programs and to access correct… more
- Kelly Services (Horsham, PA)
- …develop code lists for disease areas + Support programming deliverables for re-analysis of clinical trial data and support for any custom real world data reports ... **Oncology Real World Data Programmer ** **Summary:** The Oncology RWD Programmer will conduct statistical analyses of real-world data to address critical… more
- Harvard University (Cambridge, MA)
- …on research and teaching. Our 70+ faculty are leaders in the development of statistical methods for clinical trials and observational studies, studies on ... in these programs. Our team invites applications for a Programmer position in the National Studies on Air Pollution...SQL + Function as a resource for the Senior Programmer , to help debug programs and to access correct… more
