- Boehringer Ingelheim (Ridgefield, CT)
- …Contract Research Organizations (CROs), regulatory authorities, or academic institutions; using SAS or R; applying understanding of clinical trial development ... SAS /BASE, SAS /MACRO, SAS /GRAPH, SAS /STAT, and SAS /SQL to map raw clinical data to CDISC-compliant datasets and create TFL for data monitoring, … more
- BeOne Medicines (San Mateo, CA)
- …outputs for tables and graphs, validate statistical programs, write general SAS application codes, prepare documentation for electronic submissions, and explore new ... resource algorithm. + Oversee the work of internal and contract programmers, provide guidance, and mentoring to programmers in...+ Oversee the work of staff in support of clinical trials, ad-hoc analysis requests, data validation, etc. in… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …International Conference on Harmonization (ICH) guidelines. The SA Manager will ensure the SAs provide clinical administrative support to the study teams and ... Associate Director, will supervise a group of Study Associates ( SAs ) or Senior SAs who assist in...who assist in planning and in the execution of clinical studies in adherence to the protocol, Good … more
- Organon & Co. (Plymouth Meeting, PA)
- …**Responsibilities** + Support and manage statistical programming activities to all clinical development programs and internal initiatives. + Act as a lead ... approve data specifications for SDTM and ADaM. + Write SAS programs to generate or validate SDTM, ADaM, and...least nine years of statistical programming experience in a Contract Research Organization (CRO), biotech or pharmaceutical industry OR… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …listings, and figures (TLFs) that support the analysis and reporting of clinical trials and for providing expertise for statistical programming activities. Develop ... with cross-functional teams, and external vendors. Core responsibilities include:** + Create SAS programs to generate derived analysis datasets and content for TLFs.… more
- IQVIA (Durham, NC)
- …integrity and regulatory compliance in the application of statistical methodology to clinical trials, particularly in the area of pharmacodynamics, as they apply to ... on new or potential project opportunities, including contributing to clinical development plans, developing/reviewing protocols, preparing/reviewing analysis plans, overseeing… more
- J&J Family of Companies (Spring House, PA)
- …advanced statistical methodology in assigned projects, such as clinical trials, with demonstrated integrated disease/scientific/functional area understanding and ... partnerships with internal colleagues and with external partners (eg Contract Research Organizations (CROs), consultants, researchers/investigators) to achieve results… more
- Envista Holdings Corporation (Brea, CA)
- …efficiency. . Stay updated on industry trends and best practices in contract management and reporting. . Implement processes that enable accurate tracking of ... articulate the performance of various DSOs and ROI, making recommendations on contract renewal pricing . Present findings and recommendations to senior management… more
- AmeriHealth Caritas (Newtown Square, PA)
- …lenses that provide event triggered output for monitoring of impending contract changes and provider patterns.; + Effectively prioritizes and communicates insights ... IT, Payment Systems, Operations Services, Provider Network Management, Market, and Clinical teams as needed to research financial issues, risks, and opportunities… more
- Sumitomo Pharma (Des Moines, IA)
- …of **Senior Manager of Biostatistics** to serve as lead statistician for one or more clinical studies. He or she works closely with the clinical team on the ... + Serve as the lead statistician for one or more clinical studies, overseeing statistical design, authoring statistical sections of study protocols… more