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)Florham Park, NJThe 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.
NewIn Process Quality Inspector HYTORCIn Process Quality InspectorMahwah, NJJob Description General Purpose The In-Process / First-Piece Inspector is a critical member of the Quality Department responsible for ensuring that machined parts meet all customer, engineering, and industry requirements. W ork Environment The warehouse environment may include exposure to varying temperatures, dust, noise, and potential hazards such as moving machinery.
NewExecutive Administrator Lynkx Staffing LLCExecutive AdministratorPrinceton, NJProvide administrative support to the Executive Leadership Team including on-going weekly meeting management, management of all off-site meeting events, expense reporting related to all ELT events and purchases of collateral materials. Act as Administrator to internal operational database (QuickBase), liaising with all departments and programmer to manage all aspects of system enhancements, data entry, data mining and reporting.
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.
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.
Senior Statistical Programmer (Remote) Everest Clinical ResearchSenior Statistical Programmer (Remote)New JerseyRemoteTo drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Senior Statistical Programmer for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy. Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries.
Statistical Programmer Integrated Resources, IncStatistical ProgrammerEast Hanover, New JerseyContractorParticipate as required at all meetings, discussions and activities covering aspects of data review reporting on trial level activates. At least 2 years of work experience using SAS in the data review, analysis and/or the reporting of pharmaceutical data.
FSP Principal Statistical Programmer (Remote) Everest Clinical ResearchFSP Principal Statistical Programmer (Remote)Bridgewater, New JerseyRemoteTo drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as FSP Principal Statistical Programmer for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy. 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.
Principal Statistical Programmer (Remote) Everest Clinical ResearchPrincipal Statistical Programmer (Remote)Bridgewater, New JerseyRemoteTo drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Principal Statistical Programmer for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy. 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.
Associate Director, Statistical Programming Everest Clinical ResearchAssociate Director, Statistical ProgrammingBridgewater, New JerseyRemoteTo drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Associate Director, Statistical Programming for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy. When required, review and provide input to clinical data management deliverables including, but not limited to, the following: electronic Case Report Forms (eCRFs), eCRF Completion Instructions, data validation specifications, Data Review Plan (Plan; and the ongoing data review TLFs in accordance with the Plan), and Data Management Plan (DMP).
Senior RWE Programmer ParexelSenior RWE ProgrammerNew JerseyExpert Coder : The ideal candidate spends most of their time hands-on coding versus project management or oversight responsibilities, has hands-on experience with raw RWE data including both claims data and Flatiron EHR and can write SQL code from scratch. At least 2-3 years of experience in Real-World Data (RWD) analysis and Real-World Analytics (RWA) using healthcare claims, EMR, and/or registry databases within the biopharmaceutical industry or provider/payer organizations.
Assoc Director, Statistical Programming NovartisAssoc Director, Statistical ProgrammingEast HanoverLead statistical programming activities as a Lead/Program Programmer for a large-sized or complex project or group of projects globally or locally, or disease area with phase I to IV clinical studies in Novartis Global Drug Development. Build and maintain effective working relationships with cross-functional teams including Biostatistics and Data Management counterparts, able to summarize and discuss status of deliverables and critical programming aspects, such as,timelines, scope, and resource planning.
NewSenior Manager, Statistical Programming KardiganSenior Manager, Statistical ProgrammingPrinceton, New Jersey$172,000–$234,000 / yearThis position serves as a critical bridge between Biostatistics and Clinical Data Management (CDM), ensuring the development of CRFs and the delivery of high-quality clinical data. D., Kardigan’s co-founders have reunited after leading MyoKardia to discover and develop mavacamten, the first cardiac myosin inhibitor, resulting in an acquisition by Bristol Myers Squibb in 2020.
Senior SAS Programmer Analyst Integrated Resources, IncSenior SAS Programmer AnalystWoodcliff Lake, New JerseyContractorThis position is responsible for supporting the phase 3 clinical trial, including but not limited to, as outlined below: Reviews SAP, TLG shells and variable derivation rules and provides feedback. Develops Study Quality Surveillance Plan and monitors study conduct to proactively address issues to ensure high quality study data.
Senior SAS Programmer Integrated Resources, IncSenior SAS ProgrammerWoodcliff Lake, New JerseyContractorOur methods include applying domain expertise in specific industry segments, utilizing a highly-skilled workforce, leveraging a proven global delivery model, implementing structured and scalable quality processes and methodologies and yet, staying cost-effective. Design and develop SAS macros, applications, and other utilities to expedite SAS programming activities and usage by the Oncology Data Management and other areas of Clinical for data review.
SAS Programmer/Analyst Integrated Resources, IncSAS Programmer/AnalystEwing Township, New JerseyContractorA Few Words About Us - Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. • Analyze data results from the data pull to ensure deliverables have been met, and provide summary analysis to customer.
SAS Programmer Integrated Resources, IncSAS ProgrammerEwing Township, New JerseyContractorAdditional licensing, certifications, registrations: Knowledge: Prefer candidates have general health care knowledge Requires familiarity with DB2, ORACLE, and MS SQL Server Syntax and their purposes Requires the ability to apply more advanced knowledge and specialized skills Possesses knowledge of work activities outside own functional area. IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I Direct Line: 732-429-1920 Ext 301 Board: 732-549-2030 www.irionline.com.
Sr. Manager, Biostatistician / Programmer Legend Biotech CorpSr. Manager, Biostatistician / ProgrammerSomerset, NJManager, Biostatistician/Programmer plays a critical hands-on role in supporting Legend Biotech's clinical development programs by transforming clinical trial data into high-quality analyses, tables, figures, and listings that inform decision-making. Our research spans chimeric antigen receptor T-cell (CAR-T), T-cell receptor (TCR-T), natural killer (NK) cell-based therapies, and other emerging platforms designed to transform the treatment of serious diseases.
GenAI Programmer / AI Engineer Mitchell MartinGenAI Programmer / AI EngineerJersey City, NJ$47.49–$67.85 / hourBy applying for this job, you agree to receive AI-generated calls, text messages, and/or emails from Mitchell Martin Inc and its affiliates and contracted partners at various frequency through traditional and automated methods. • A top financial services firm is seeking a hands-on GenAI Engineer for a high-visibility Generative AI initiative focused on enterprise-scale document summarization and conversational AI.