- Bristol Myers Squibb (Trenton, NJ)
- …**Experience Requirements** + Minimum of 4 plus years Pharmaceutical/CRO experience as a SAS Programmer supporting clinical trials for regulatory submissions ... 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
- Ascendis Pharma (Palo Alto, CA)
- …for employees to grow and develop their skills. The Clinical Data Programmer will be responsible for performing SAS programming ( SAS /SQL program ... clinical data review and process efficiency. The Clinical Programmer will lead clinical ...other department members on data review tools such as SAS . + Collaborates with clients, peers, programmers ,… more
- Actalent (Boston, MA)
- Remote SAS Programmer ( senior and principal levels)Location: Remote (East Coast candidates only)Position Type: Full-TimeAbout Us: Actalent is a company that ... a more advanced future. Role Overview: As a Remote SAS Programmer , you will play a pivotal...programming. This position offers a unique opportunity for experienced SAS programmers who thrive in a dynamic… more
- IQVIA (Philadelphia, PA)
- … 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:** + 8 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
- AbbVie (North Chicago, IL)
- …all process improvements are implemented. + Utilize expertise in the use of the SAS Macros developed for the Statistical Programmers . + Participate in the ... for Analyst Data Models (ADaM), Study Data tabulation Models ( SDTM ), and Tables, Listings, and figures. + Assist in...testing etc.; (iv) experience in the use of the SAS Macros developed for the Statistical Programmers .… 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
- AbbVie (Boston, MA)
- …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
- Merck (North Wales, PA)
- …+ Experience with study data standards CDISC ( SDTM ) + Experience in SAS and clinical programming. + Knowledge and experience in developing analysis and ... **Job Description** The Senior Statistical Programmer , Study Data Tabulation Model ( SDTM ),...Sciences, Engineering with a minimum of five (5) years SAS programming experience in a clinical trial… 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 Senior 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
- Kelly Services (Rochester, NY)
- …timelines. + Communicate/discuss data/analysis issues with team of programmers ( SAS and Data Management), statisticians, and clinical managers. + Serve ... **Biostatistician** Kelly(R) Science & Clinical is seeking a Biostatistician for our client...as technical resource to study teams. + Ensure CDISC/ SDTM datasets and define documents are appropriately prepared for… more
- Actalent (Seattle, WA)
- …statistical software such as SAS or R. + Strong knowledge of CDISC SDTM and ADaM + Working knowledge of clinical trial design, statistical methodologies, and ... expertise will contribute to the analysis and interpretation of clinical studies. As a vital part of our team,...will partner with other stakeholders in studies including statistical programmers and data managers. Key Role and Responsibilities: +… more