Quality Control CMM Programmer CNC Manufacturing IncQuality Control CMM ProgrammerCoatesville, PA$30–$35 / hourFull timeStrict Statistical Process Control (SPC) procedures further ensure the highest quality results, which when combined with streamlined project management expertise, have earned CNC Manufacturing (including sister company, CNC Technology) the coveted DEKRA ISO 9001:2015 certification. The 37,000 sq ft facility in Coatesville, PA features some of the industry’s most technologically advanced machining and quality control equipment, enabling CNC Manufacturing to deliver precise parts within the tightest of tolerances.
NewCNC Machine Setup Programmer CNC Manufacturing IncCNC Machine Setup ProgrammerCoatesville, PAStrict Statistical Process Control (SPC) procedures further ensure the highest quality results, which when combined with streamlined project management expertise, have earned CNC Manufacturing (including sister company, CNC Technology) the coveted DEKRA ISO 9001:2015 certification. The 37,000 sq ft facility in Coatesville, PA features some of the industry’s most technologically advanced machining and quality control equipment, enabling CNC Manufacturing to deliver precise parts within the tightest of tolerances.
NewMetrology Programmer Everforth, CybercodersMetrology ProgrammerSomerset, NJ$80,000–$98,000 / yearThis role supports production and quality engineering by translating GD&T requirements and blueprints into reliable inspection routines, conducting First Article Inspections (FAIs), supporting PPAP submissions, and applying SPC/MSA practices to drive continuous improvement in measurement processes. The Metrology Programmer develops, validates, and maintains automated inspection programs and routines for vision and optical metrology systems to ensure product conformance to engineering drawings and specifications.
NewCMM Programmer/ Operator - 1st Shift GA RichardsCMM Programmer/ Operator - 1st ShiftSpring Lake, MIWhile performing the duties of this Job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; stoop, kneel, crouch, or crawl and talk or hear. Summary: Operate the Coordinate Measuring Machine to perform dimensional lay-outs for the Production Part Approval Process (PPAP), internal and customer-requested capability studies, and other measuring requirements.
NewSr. Manager, Statistics Takeda PharmaceuticalSr. Manager, StatisticsBoston, MARemote$137,000–$215,270 / yearManager, Statistics with the following duties: provide statistical support in the design, analysis, and interpretation of clinical trials to enable quantitative decision-making at a compound level for Takeda oncology programs; independently represent statistics function on global teams in support of drug development; develop and review the study synopsis, protocol, statistical analysis plan, clinical study report, and other regulatory submission documents, ensuring accurate and statistically valid deliverables; leverage internal and external resources to achieve quality, timely and cost effective compound level and submission deliverables; plan and direct compound level analysis and reporting activities including work of other statisticians and programmers; monitor and contribute to industry advances in statistical methods to optimize study designs and statistical analysis methods, and implement innovative approaches at a compound level. Any individual may provide documentary evidence bearing on this application, with information on available workers and information on wages and working conditions, to the Certifying Officer, U.S. Department of Labor, Employment and Training Administration, Office of Foreign Labor Certification, 200 Constitution Avenue, NW, Room N-5311, Washington, DC 20210.
Associate Director, Biostatistics (Late Stage Oncology) Daiichi Sankyo, Inc.Associate Director, Biostatistics (Late Stage Oncology)Basking Ridge, NJ$175,440–$263,160 / yearFull timeProtocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies including study design, protocol development, CRF review, SAP development, analysis files development, statistical analysis accuracy validation, results interpretation and CSR input and review. Global BDO Strategy to Improve Drug Development: Primarily participates and may occasionally lead moderately complex initiatives, with some level of supervision, to improve the harmonization and efficiency of drug development which leads to cost savings and shortened timelines for the company.
NewAssociate Director - Data Standards (Hybrid) AbbVieAssociate Director - Data Standards (Hybrid)Irvine, CAThe amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio.
Statistical Programmer/Sr. Statistical Programmer Arrowhead PharmaceuticalsStatistical Programmer/Sr. Statistical ProgrammerLos Angeles, CA$90,000–$135,000 / yearArrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes.
Statistical Programmer III/IV Fred Hutchinson Cancer CenterStatistical Programmer III/IVSeattle, WashingtonRemote$99,486–$157,227 / yearFull timeSCHARP is seeking a Statistical Programmer III/IV to provide statistical programming expertise within SCHARP by coordinating with statisticians to write efficient, re-usable, and easily maintainable code that access, analyze and report data descriptives and analyses. With a track record of global leadership in bone marrow transplantation, HIV/AIDS prevention, immunotherapy and COVID-19 vaccines, Fred Hutch has earned a reputation as one of the world’s leading cancer, infectious disease and biomedical research centers.
Senior Statistical Programmer LancesoftSenior Statistical ProgrammerIrvine, CA$75The Senior Statistical Programmer Contractor is expected to work independently, deliver high quality programming deliverables, and collaborate effectively with Biostatistics and Clinical Data Management. Primary ResponsibilitiesDevelop complex analysis datasets, specifications, and summary outputs (tables, listings, figures, and graphs) for inclusion in clinical study reports, regulatory submissions, and internal presentations.
NewContractor – Principal Statistical Programmer Syndax PharmaceuticalsContractor – Principal Statistical ProgrammerNew YorkRemoteThe Principal Statistical Programmer performs the statistical programming required for analysis of clinical trial data on projects for in-house and out-sourced clinical trials, commercial requests, Health Economics Outcome Research (HEOR) analyses, pooled analysis such as integrated summary of efficacy (ISE) and integrated summary of safety (ISS) and any ad-hoc analyses as required. The Principal Statistical Programmer will provide expert-level hands-on programming support and technical expertise to develop, maintain, validate, and execute SAS programs that access, visualize, analyze, and report clinical trial data in accordance with statistical analysis plans, ICH guidelines, and applicable regulatory requirements.
Sr.Statistical Programmer Karwell TechnologiesSr.Statistical ProgrammerBoulder, COThe Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and documenting SAS programs to generate analysis datasets, data listings, summary tables, and statistical graphs supporting statistical analyses. Support submission activities including preparation of data packages, eCTD deliverables, and responses to regulatory agencies, Communicate with team members about statistical programming related to trial timelines, data quality, and results interpretation.
Principal Statistical Programmer Vertex PharmaceuticalsPrincipal Statistical ProgrammerBoston, MassachusettsRemote$149,200–$223,800 / yearEngages with a variety of other functions, including Statistical Programmers, Biostatisticians, Data Management, and other departments engaged in providing data and submission-related activities, often at Senior Management levels. Solves complex clinical trial reporting problems and demonstrates technical proficiency and exercises judgment in supporting daily operations and ensuring that study tasks are completed accurately and in a timely manner.
Sr.Statistical Programmer Katalyst Healthcares & Life SciencesSr.Statistical ProgrammerBoulder, COThe Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and documenting SAS programs to generate analysis datasets, data listings, summary tables, and statistical graphs supporting statistical analyses. Support submission activities including preparation of data packages, eCTD deliverables, and responses to regulatory agencies, Communicate with team members about statistical programming related to trial timelines, data quality, and results interpretation.
Lead Statistical Programmer Karwell TechnologiesLead Statistical ProgrammerNewark, NJProvide leadership, project specific training, stakeholder management, external sponsor support, resource management, and project management for the required programming tasks supporting clinical trial activities. Create statistical analysis outputs to be used in support of final reports, abstracts, posters, Manu scripts, and other clinical publications; support systems to produce electronic regulatory submissions.
Statistical Programmer SystimmuneStatistical ProgrammerRedmond, WAFull timeIt specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). Qualifications Master’s degree or higher in Biostatistics, Statistics, Mathematics, or a related scientific discipline, with 0–2 years of experience in statistical programming within the pharmaceutical/biotech industry or a CRO.
Lead Statistical Programmer Katalyst Healthcares & Life SciencesLead Statistical ProgrammerNewark, NJProvide leadership, project specific training, stakeholder management, external sponsor support, resource management, and project management for the required programming tasks supporting clinical trial activities. Create statistical analysis outputs to be used in support of final reports, abstracts, posters, Manu scripts, and other clinical publications; support systems to produce electronic regulatory submissions.
Sr. Statistical Programmer Katalyst Healthcares & Life SciencesSr. Statistical ProgrammerBaltimore, MDThe Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and documenting SAS programs to generate analysis datasets, data listings, summary tables, and statistical graphs supporting statistical analyses. Support submission activities including preparation of data packages, eCTD deliverables, and responses to regulatory agencies, Communicate with team members about statistical programming related to trial timelines, data quality, and results interpretation.
Senior Statistical Programmer Katalyst Healthcares & Life SciencesSenior Statistical ProgrammerLake county, ILThe Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and documenting SAS programs to generate analysis datasets, data listings, summary tables, and statistical graphs supporting statistical analyses. Support submission activities including preparation of data packages, eCTD deliverables, and responses to regulatory agencies, Communicate with team members about statistical programming related to trial timelines, data quality, and results interpretation.
Principal Statistical Programmer IQVIAPrincipal Statistical ProgrammerDurham, North CarolinaIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).