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.
NewCmm Programmer AerotekCmm ProgrammerAnaheim, CA$33–$40 / hourSince 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Job Description Job Title: CMM Programmer Job Description The CMM Programmer is responsible for developing, maintaining, and executing CMM inspection programs used to inspect materials, tooling, and manufactured parts for compliance with engineering drawings and quality requirements.
NewDatabase analyst/programmer 2- #100450 Swoon Staffing West CoastDatabase analyst/programmer 2- #100450Peoria, ILPosition’s Contributions to Work Group : The position fills the Database Administrator (DBA) role for a small analytics team, maintaining the intended data architecture (including for other team members), implementing data governance, creating and managing database objects, and documenting the architecture and program-specific flows. Own end-to-end user access management: triage access requests, obtain approvals/denials, communicate results, grant access, and administer role-based access controls to keep users accountable and compliant.
NewContract CMM Programmer/Operator ExpressPros - Amherst, OHContract CMM Programmer/OperatorLorain, OH$30–$40 / hourWhile performing the duties of this job, the employee is regularly required to use hands and fingers to handle, feel, or operate objects, tools or controls, and reach with hands and arms. Project Candidate responsible for part layout, developing CMM programming and dimensional reports from CMM data for the PPAP (production part approval process) review program.
NewQuality Control CMM Programmer CNC Manufacturing IncQuality Control CMM 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.
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.
NewBiostatistics Consultant - Contract TalentBurst, Inc.Biostatistics Consultant - ContractMarlborough, MARemote$68–$69.20 / hourResponsibilities include reviewing and finalizing analysis datasets, supporting data quality and consistency checks, conducting or validating statistical analyses, generating tables, figures, and listings, interpreting statistical results, and contributing to statistical content to be used for publications. Essential Functions, Knowledge, and Skills Lead Statistical Efforts: Serve as the primary biostatistician for a study within a project team, supporting closeout activities and reviewing, validating, and executing analyses.
NewAssociate Director, Biostatistics Clinical Dynamix, Inc.Associate Director, BiostatisticsBurlington, MAspecific responsibilities while upholding our core working behaviors of Trust and Respect, Communication and Feedback, Accountability and Reliability, Objectivity, and Team Balance and. •Provide high-quality statistical support across clinical programs, ensuring scientific.
Associate Director, Epidemiology Analytics Daiichi Sankyo, Inc.Associate Director, Epidemiology AnalyticsBasking Ridge, NJ$157,920–$236,880 / yearFull timeProvide data management of diverse data (e.g., real-world setting and clinical trial) to set up epidemiologic data sets for various approaches, quantitative epidemiologic data analysis, interpretation of results, visualization of results, and generate manuscripts to disseminate findings. Doctorate Degree (PhD) in Biostatistics, Data Science, Statistics, Applied Mathematics, Epidemiology or related field plus a minimum of 4 years of experience in epidemiologic methods and data analysis (pharmaceutical industry in safety or associated service provider experience is preferred).
NewAssociate Director - Data Standards (Hybrid) AbbVieAssociate Director - Data Standards (Hybrid)North Chicago, ILThe 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.
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 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.
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.
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 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.
Lead Statistical Programmer Katalyst Healthcares & Life SciencesLead Statistical ProgrammerSan Francisco, CAProvide 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.
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.
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.