lead statistical programmer

Responsibilities: Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs. Be responsible for overall project delivery, including clinical trial reports and other regulatory submission deliverables. Create statistical analysis outputs to be used in support of final reports, abstracts,...

Job Summary: The Contract Lead Programmer serves as a senior, hands-on programmer responsible for managing statistical programming activities across multiple clinical trials and therapeutic areas. The role oversees external CRO partners to ensure high-quality, timely, and compliant delivery of analysis datasets, tables, listings, and figures that...

Responsibilities: Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs. Be responsible for overall project delivery, including clinical trial reports and other regulatory submission deliverables. Create statistical analysis outputs to be used in support of final reports, abstracts,...

Responsibilities: Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs. Be responsible for overall project delivery, including clinical trial reports and other regulatory submission deliverables. Create statistical analysis outputs to be used in support of final reports, abstracts, posters,...

Responsibilities: Lead the development, validation, and documentation of CDISC-compliant SDTM and ADaM datasets for CNS clinical trials, ensuring traceability from raw data through analysis outputs. Program and QC tables, listings, and figures (TLFs) for interim and final clinical study reports, regulatory submissions, and client deliverables. ...

Statistical Programmer Lead the development, validation, and documentation of CDISC-compliant SDTM and ADaM datasets for CNS clinical trials, ensuring traceability from raw data through analysis outputs. Program and QC tables, listings, and figures (TLFs) for interim and final clinical study reports, regulatory submissions, and client deliverables. Interpret...

Planet Pharma is seeking a Senior Statistical Programmer to lead programming activities for global clinical trials and support regulatory submissions. The role focuses on delivering high-quality SDTM and ADaM outputs, developing SAS macros, and guiding cross-functional teams within a Biometrics Center of Excellence. Ideal candidates will have 4+ years of...

ViiV Healthcare in the United States seeks a Principal Statistical Programmer to lead programming for complex studies, ensuring high-quality development, validation, and delivery of analysis outputs. You will drive technical excellence, innovation, and standards adoption while mentoring junior programmers. This role offers strategic input on study data,...

Providing senior-level leadership and technical direction, the full-time remote Lead Data Manager/SAS Programmer will manage data management and statistical programming for clinical research and epidemiological studies, ensuring data quality and integrity while mentoring staff and promoting standardized practices.Key responsibilitiesProvide oversight for...

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in...

Responsibilities: The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data. The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions to support clinical data analysis and reporting ...

Responsibilities and Requirements: Experience working in various disease areas. They also must have specific expertise in SDTM programming, have submissions experience, and MUST possess strong skill in graphing. They need to be comfortable working as a strong independent contributor who is attentive and speaks up throughout the project work. Minimum of 5...

Job DescriptionCandidate to develop standard global data review tools, such as patient profiles, data quality checks, exception reports, PD reports, listings and figures for oncology trials.Ensure timelines and adequate quality of data review reporting deliverables for assigned trials. Follow processes and adhere to Client and project specific standards as...

Company DescriptionIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide...

Responsibilities: Develop SAS programs and statistical output for the management and reporting of clinical trial data managed by GCD Guarantee quality of statistical output produced by external provider, to program tools to support data review activities and data visualization, to collaborate on the interpretation and communication of trial...

Requirements: B.Sc., M.Sc., or equivalent education in Biostatistics/Statistics, Bioinformatics, Life Sciences, Mathematics, Physical Sciences, or related fields Advanced SAS macro programming experience is required for the development of global tools that will increase the efficiency and capacity of the Statistical Programming group At...

Company DescriptionABOUT THE COMPANY:A design company that blends technology, creativity and engineering to help customers transform ideas into world-class products and solutions. The company addresses the communications, consumer products, defense, healthcare, media & entertainment, semiconductor and transportation sectors. This is supported by a network of...

We are the people who give possibilities purposeBD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per...

Senior Statistical Programmer We are seeking a highly motivated and qualified individual to join our Clinical Department as a Senior Statistical Programmer and work as part of a team to drive success. Ideal candidates will be self-motivated, independent, committed to the generation of high-quality data within a fast-paced and innovative research team. The...

Responsibilities: Ensure departmental or functional training plans in place and appropriate Perform vendor qualifications regarding statistical programming functions and manage CRO programming issues and activities to ensure on time deliverables within budget Generate, validate, and/or review SDTM domains and ADaM datasets and...