- Merck & Co. (North Wales, PA)
- …a key collaborator with internal and external stakeholders including Statistics, Clinical Research, Regulatory, Observational Research, Clinical Safety and PK/PD ... operational challenges that require strategic solutions, resulting in improved Clinical Study Report and filing completion timelines worldwide.Lead development of… more
- Merck & Co. (North Wales, PA)
- …be programmed, an understanding of statistical terminology and concepts.Familiarity with clinical data management conceptsExperience in CDISC and ADaM ... Specific Required Skills and Experience: Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH;… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …training and ensure effective implementation of SDTM, ADaM and TLFs standard in clinical trial data analysis- Develop and maintain necessary programming macros ... 2025 Vision to become a "Global Pharma Innovator with Competitive Advantage in Oncology ," Daiichi Sankyo is primarily focused on providing novel therapies in … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …collaborates closely with data manager to ensure high quality data . Work closely with internal statistical programmer .Drug Development Strategy: Provides ... 2025 Vision to become a "Global Pharma Innovator with Competitive Advantage in Oncology ," Daiichi Sankyo is primarily focused on providing novel therapies in … more
- Ascendis Pharma (Palo Alto, CA)
- …We are a dynamic workplace for employees to grow and develop their skills. The Clinical Data Programmer will be responsible for performing SAS programming ... data review and process efficiency. The Clinical Programmer will lead clinical ...using BASE/SAS, SAS/STAT, SAS MACROS + Strong knowledge of Oncology clinical trials + Data … more
- Merck (Rahway, NJ)
- …a key collaborator with internal and external stakeholders including Statistics, Clinical Research, Regulatory, Observational Research, Clinical Safety and PK/PD ... Address operational challenges that require strategic solutions, resulting in improved Clinical Study Report and filing completion timelines worldwide. + Lead… more
- Merck (Rahway, NJ)
- …be programmed, an understanding of statistical terminology and concepts. + Familiarity with clinical data management concepts + Experience in CDISC and ADaM ... Specific Required Skills and Experience:** + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH;… more
- Lilly (IN)
- … Study Build Programmer is responsible for programming and testing clinical trial data collection databases, including the mapping, testing and normalization ... data flow, data standards, database programming, normalization and testing. The Clinical Study Build Programmer will collaborate with Data and… more
- University of Michigan (Ann Arbor, MI)
- App Programmer /Analyst Senior/Inter Apply Now **Summary** The Judith Tam ALK Lung Cancer Research Initiative is a new initiative in the Rogel Cancer Center focused ... generated in the overall research effort as well as mine relevant published data from public resources. **Why Join Michigan Medicine?** Michigan Medicine is one of… more
- IQVIA (Philadelphia, PA)
- …database components and theory. + Excellent application development skills. + Strong understanding of clinical trial data and extremely hands on in data ... client requirements. **Job Details:** + Position: - Principal Statistical Programmer + Home Based + Min 4+ years of...Min 4+ years of CRO/Pharma Industry + Therapeutic Areas: Oncology // Immunology // IDV // EDCP **Key Skills:**… more
- AbbVie (North Chicago, IL)
- …remarkable impact on people's lives across several key therapeutic areas - immunology, oncology , neuroscience, and eye care - and products and services in our ... of case report forms (CRFs), database definitions, and specifications for analysis data sets for individual studies. + Ensure accuracy of database quality assurance… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …be for you if have:** + Proficiency in SAS programming skills in a clinical data environment with excellent analytical skills. Knowledge of other programming ... The Manager Statistical Programmer will lead and support all programming activities...with 8+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …training and ensure effective implementation of SDTM, ADaM and TLFs standard in clinical trial data analysis - Develop and maintain necessary programming macros ... 2025 Vision to become a "Global Pharma Innovator with Competitive Advantage in Oncology ," Daiichi Sankyo is primarily focused on providing novel therapies in … more
- Amgen (Washington, DC)
- …and are statistically accurate. The Biostatistical Programming Senior Manager (Product Lead Programmer ) lead a group of Oncology and other therapeutic area ... + Prior regulatory submission experience + Thorough understanding and experience with data quality and compliance checks + Experience in software development (eg,… more
