Statistical Programmer Salary at Sumptuous Data Sciences Llc BETA

Job Duties: Expert in addressing technical challenges that connect SAS, CDISC and XML. Excellent technical skills in SAS system and application development. Proven experience in development and implementation of clinical standards in a global pharmaceutical environment. Expert in integrating SAS with other leading technologies such as PDF, XML, Microsoft Office, to support electronic submissions. Experience in consulting projects dealing with the assessment, design and/or implementation of CDISC data standards in the clinical data life cycle. Annotate CRFs in accordance with CDISC published or company specific guidelines with appropriate metadata to reflect case report tabulation data sets. Review and quality assure CRF annotations produced by other programmers Embrace and contribute to our culture of process improvements with a focus on streamlining our processes adding value to our business needs. Review and quality assure data set and programming specifications produced by other pro

Job Description Job Description Job Description Company Descriptions: Wizsolution is located in Princeton NJ, which is a leader in pharmaceutical recruitment and staffing. Our goal is to provide effective solutions for fulfilling your career potential. The mission of our company is to connect high talent and motivated candidates to technical positions from our partner companies. Job descriptions: Senior SAS Programmer Senior Statistical Programmer * -Perform SAS data manipulation and analysis programming -May work with medical writing, clinical operations, and other clinical staff to support deliverables. -Must work well both independently and with team members. -Needs to be able to be on-time with deliverables, and for those deliverables to be of quality. -Works with Statistician and Statistical programmer to assure results are consistent with expectations, and Quality control procedures are followed. -Plans and carefully documents differences between programming results between progr

Responsibilities: The Senior Statistical Programmer I will assist the US and/or EU Early Phase Statistical Programming teams by developing SAS programs for analysis datasets. They will be responsible for listing and safety summary tables, providing project tracking information to the team, addressing any validation comments, documenting programming activities, acting as a subject matter expert (SME) within the SAS Programming team, and mentor/train other junior team members. Lead and manage the assigned programming team's deliverables at the study and program level to ensure project objectives are met within budget, to agreed timelines, and to the highest standard of quality. Program analysis datasets, listings, and tables without supervision. Serve in a client-facing capacity that demonstrates the ability to anticipate client needs and implement innovative solutions. Facilitate flow of information on study budgets and change order management in a timely and efficient manner. Liaise ef

**Position Title: Senior Biostatistician** **Join a Legacy of Innovation 125 Years and Counting!** Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 18,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. In addition to a strong portfolio of medicines for cardiovascular diseases, under the Groups 2025 Vision to become a Global Pharma Innovator with Competitive Advantage in Oncology, Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. **Job Summary:** Position leads statistical support for low

We have a current opportunity for a AD Biostatistics on a permanent basis. The position will be based in New Jersey (3x a week). For further information about this position please apply. Job Title: Associate Director of Biostatistics Location: New Jersey, USA | 3x a week on site Company Overview: We are a dynamic and innovative biotech company focused on developing cutting-edge therapies in the fields of oncology and central nervous system (CNS) disorders. Our mission is to bring life-changing treatments to patients through rigorous scientific research and clinical excellence. Position Summary: The Associate Director of Biostatistics will play a pivotal role in our clinical development programs, providing statistical leadership and expertise in the design, analysis, and interpretation of clinical trials. This position will collaborate closely with cross-functional teams to ensure the integrity and accuracy of our clinical data, ultimately supporting the advancement of our oncology and

Responsibilities: Participate in developing and maintaining clinical trial data and statistical programming standards to ensure the company standards are up to date and in line with pharmaceutical industry standards, conventions, and regulatory requirements. Perform hands on primary statistical programming and validation programming on assigned projects including but not limited to phase I - IV clinical trials, integrated clinical summaries, responses to requests from regulatory agencies, publication support, data explorations, data monitoring committee meetings, etc. Create SDTM mapping specifications and ADaM data specifications. Perform quality control (QC) review of these documents prepared by others. Create SDTM and ADaM define.xml files. Perform QC review of these files prepared by others. Perform 3rd level QC review on programming deliverables before their release to the clients. Perform QC review/assessment on regulatory submission programming documents, datasets, tables/listin

Job Description Job Description Minimum Requirements | Role Responsibilities · Expertise in extracting, manipulating, summarizing, analyzing, and presenting data using SAS procedures· Expertise in SAS/MACRO, SQL, and SAS/BASE procedures· Expertise/experience in use of SAS/GRAPH and Statistical procedures· Highly experienced working in Clinical data and medical dictionaries· Knowledge of relational database principles· Able to program in Linuxenvironment· Strong understanding of clinical trials – how programming deliverables fit in to the process, what types of data are collected· Data structure understanding (BDS – Basic Data Structure, CDISC SDTM and ADaM)· Able to draft programming requirements from statisticalanalysis plan· Strong experience with studyreporting· Previous experience using CDARS –Preferable· Preferred Masters (US) BSc (Europe) in | · Create submission-ready standard data presentations and data sets using standard coding· Create submission-ready non-standard data prese

Responsibilities: Utilize SAS to generate and validate tables, listings, and figures (TLF) based on SAP. Use major statistical programming language to perform data analysis for various needs. Provide statistical analysis support for post approval studies. Evaluate and ensure CDISC compliance with study tabulation and analysis data files. Write specifications and statistical programs to generate analysis datasets and outputs. Perform data analysis tasks with minimal supervision. Provide programming support for data management. Develop statistical toolbox for advanced data modelling, tabulation, and visualization. Participate in reviewing and validating data analysis results. Requirements: Strong SAS programing skill in producing various types of outputs such as TLFs and datasets with minimum of 3 years of experiences. Extensive statistical programming experience in producing deliverables either on a scheduled or ad hoc basis. BS degree in Statistics, Mathematics, Computer Science, or re