- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …, ADaM dataset and TLFs, support technical training and ensure effective implementation of SDTM , ADaM and TLFs standard in clinical trial data analysis- Develop ... utility development preferred- Advanced working knowledge of all aspects of the SAS programming language used in clinical trials programming preferred- Advanced… more
- DivIHN Integration Inc (Deerfield, IL)
- …regarding the following opportunity, please contact our Talent Specialists Meghna at ### Title: Clinical SAS Programmer Location: Deerfield, IL Duration: 12 ... specifications, statistical analysis plans, tables, listings, and figures (TLF) shells, SDTM /ADaM specifications, clinical study reports, and other relevant… more
- Bristol Myers Squibb (Trenton, NJ)
- …Requirements** " + Minimum of 4 plus years Pharmaceutical/CRO experience as a SAS Programmer supporting clinical trials for regulatory submissions with ... appropriate metadata to reflect tabulation datasets + Oversee/ develop SAS programs to generate SDTM datasets +...SDTM with an end to end understanding of clinical drug development lifecycle. Please see job description for… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …, ADaM dataset and TLFs, support technical training and ensure effective implementation of SDTM , ADaM and TLFs standard in clinical trial data analysis - Develop ... developing tools and macros and build up standard on SDTM /ADaM datasets, and TFLs. **Responsibilities** - Supporting project lead...- Advanced working knowledge of all aspects of the SAS programming language used in clinical trials… more
- General Dynamics Information Technology (NC)
- …Citizenship Required:** Yes **Job Description:** **GDIT's Military Health team is hiring a SAS programmer to support the Office of Regulated Activities (ORA) ... versions) for CDISC datasets; Develop SEND datasets conforming to CDISC standards (non- clinical data); Develop SDTM datasets conforming to CDISC standards;… more
- IQVIA (Austin, TX)
- … Graph and SAS Macro Language + Should have experience with SDTM Implementation and ADaM implementation according to CDISC Standards. + Must have expertise in ... **Location: Homebased anywhere in the US** **Purpose:** Experienced R programmers needed to provide technical expertise to develop process methodology for department… more
- IQVIA (Durham, NC)
- …maintaining good client relationships. **Our expectations of you:** + 9 years or more in SAS programming for clinical trial data, working within a CRO or Sponsor ... We are now expanding this team by adding a Principal/Lead level Statistical Programmer . Expect to be dedicated to this sponsor, working within their environment and… more
- WCG Clinical (Princeton, NJ)
- …required **QUALIFICATIONS/EXPERIENCE:** + At least five years of post-Bachelor's experience in Clinical SAS Programming, analyzing data, working in a team ... Review deliveries. + Serve as mentor for less experienced programmers . + Lead SAS training sessions for...environment, and participating in managing projects. + Extensive SAS programming in a clinical trial setting… more
- Medtronic (Minneapolis, MN)
- …and Study Data Tabulation Model ( SDTM ) for electronic submissions. Coordinate clinical database analysis programming utilizing SAS on multiple platforms for ... Statistical Programmer Analyst for Medtronic, Inc. Minneapolis, MN. Provide clinical and statistical knowledge and software programming expertise as part of the… more
- ICON Clinical Research (Blue Bell, PA)
- …need:** + 8+ years of experience successfully performing the role of Statistical Programmer , in the clinical research industry + Experience with leading multiple ... ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we...We have an incredible opportunity for a **Senior Statistical Programmer II** to join the diverse and dynamic team… more
- IQVIA (Durham, NC)
- …+ Proficient in data visualization software - Spotfire, R/R Shiny. + Demonstrates SAS programming proficiency. + Knowledge of clinical trial study design and ... work in a data visualization team, safety statistical programming. The statistical programmer works collaboratively with the end users, internal colleagues to ensure… more
- AbbVie (North Chicago, IL)
- …of relevant experience. + Previous experience leading a team of statistical programmers . + In-depth understanding of SAS programming concepts and techniques ... safety data sets and providing technical guidance to team of Statistical Programmers in the research, development, and safety assessment of pharmaceutical products.… more
- IQVIA (Durham, NC)
- …Reporting Standards. Candidates should be experienced Biostatisticians or Statistical Programmers capable of the skills and responsibilities described below. This ... standardization activities and departmental initiatives. + Works with-in the Global Clinical Data Standards team in collaboration with each data state: Data… more
- Ascendis Pharma (Palo Alto, CA)
- …of CDISC SDTM , ADaM datasets, and Tables, Listings, Figures for clinical study reports, ISS, or ISE for assigned projects. Independently provide programming ... The Manager, Statistical Programmer will be expected to provide timely support...programming support for all of required deliverables. + Process clinical data required for statistical analysis. Develop SAS… more
- WuXi AppTec (San Diego, CA)
- …derivation rules for data integration. + Provide high level input to statistical analysts/ programmers to prepare CDISC compliant SDTM and ADaM datasets + Conduct ... position are toprovide leadership in planning and conducting data analyses in clinical studies, and participate in planning and data analyses for regulatory… more
