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- ...several positions for contract research in Clinical trials of drugs, biologics and medical... ...: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH... ...and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs...SASContract workImmediate start
- Sr. Clinical SAS Programmer job at cGxPServe. Newark, NJ. Responsibilities: Perform data manipulation, analysis, and reporting of clinical trial data. Develop and maintain department/system-level macros. Create and review SDTM and ADaM specifications. Create and validate...SAS
- Mandatory: SDTM, SAS Looking for 5+ years of clinical SAS programmers having in depth knowledge of CDISC SDTM. Gathering data from all available sources and using SAS to process it. Creating and writing programs. Preparing and presenting operations reports to the management...SAS
- ...role in driving data integrity and analytical excellence across clinical development programs. The group fosters a collaborative and innovation... ...and Biostatistics teams. Build and maintain robust SAS macros and utilities to optimize workflows. Ensure quality, consistency...SASFull timeContract work
Axiom Path
Bridgewater, NJ7 days ago $114.7k - $180.5k
Job Description Senior Statistical Programmer - Early Development Statistics and PK/PD Modeling Responsibilities This... ...Sciences, Engineering, or related field plus 5‑9 years SAS programming experience in a clinical trial environment. MS in Computer Science, Statistics...SAS$114.7k - $180.5k
...activities for late stage drug/vaccine clinical development projects. This may include leadership... ...or related field plus 5 years SAS programming experience in a clinical trial... ...the program development effort of other programmers; experience as a programming mentor Ability...SASWorldwide- Join to apply for the SAS Programmer role at Katalyst CRO . Overview Responsibilities Develop and validate programs that create datasets... ...study complexity, ensuring adherence to ICH guidelines, Good Clinical Practices, and regulatory requirements. Mentor junior programmers...SASFull timeContract work
- ...summary: The role of the Senior Statistical Programmer is to perform statistical programming activities for all assigned Phase I-IV clinical studies. This includes statistical... ...experience in statistical programming with SAS in a pharmaceutical or CRO environment. Bachelors...SASPermanent employment
- ...positions from our partner companies. Job descriptions: Senior SAS Programmer Senior Statistical Programmer * -Perform SAS data... ...and analysis programming -May work with medical writing, clinical operations, and other clinical staff to support deliverables....SASFull time
- ...deliverables under the guidance of a senior level programmer. Perform validation tasks according to... ...and regulatory submissions. Produce SAS transport files and associated... ...2 years SAS programming experience in a clinical trial environment. Must possess SAS programming...SASRemote work
- Overview Statistical Programmer at Katalyst CRO. This role involves developing SAS programs and statistical output for management and reporting of clinical trial data, ensuring quality of outputs, contributing to regulatory submissions, and supporting data review and interpretation...SASContract work
- ...POSITION: Sr. Statistical Programmer Provide programming support to clinical studies and submissions Develop and maintain programs to produce and/or validate... ...ADaM IG and SAP Develop, maintain, and understand SAS macros and other utility programs Design, develop,...SASRemote jobContract workWork experience placement
- ...programming and validation support for clinical study reports and help coordinate programming... ...with Biometrics lead and other study programmers to meet timelines. • Ensure quality of... ...in clinical research, ideally as a SAS programming for phase I-IV clinical trials...SAS
- ...data streams including (but not limited to) clinical registry reporting files (e.g. Clintrials... ...Point of Contact, Janssen project lead programmer. Requirements: Programming or... ...level experience in the implementation of SAS (Base and Macro) in the analysis of clinical...SASContract workLocal areaRemote work
- Overview Position: SAS Programmer Location: Onsite work in Raleigh, NC (Local only) Contract: 12+ Months Contract Job Description Quality... ...health data can be leveraged to derive insights that inform clinical o Sample Role Types: Technical Specialist, Product...SASContract workLocal area
$112.97k - $122k
Statistical Programmer (Data & Statistical Sciences (DSS)) Apply for the Statistical Programmer (Data... ...pharmaceutical products. Analyze & report clinical trial data under the direction of Senior Statistical Analyst. Provide SAS programming support for clinical trials. Develop...SASTemporary workRemote workWork from home3 days per week- Statistical Analyst and SAS Programmer job at R&G US Inc.. Somerset, NJ. R&G US Inc. is a leading Contract Research Organization (CRO) providing full services for clinical trial and entire drug life cycle. Led by former FDA experts and industry experts, R&G US can provide...SASPermanent employmentContract work
- The Senior Programmer is responsible for managing the inflow of a variety of healthcare claims and EMR databases, checking quality, developing... ...are strongly desired, as well as experience with SQL, Python, SAS, and visualization tools such as Spotfire. In addition...SASRemote work
- Lead Statistical Programmer (Edison, NJ) Lead Statistical Programmer (Edison, NJ) to manage statistical programming activities across clinical studies; evaluate protocols and case report forms; program... ...figures (TLFs); convert existing SAS programs to R; develop R Shiny...SASRelocation
- ...looking for a CDISC expert/SME who can handle business queries. The candidate must be very good in SDTM. Qualifications: 10+ years of clinical SAS programming experience with in-depth knowledge of CDISC SDTM. Responsibilities: Gathering data from all available sources and...SAS
- ...Description Job Description We are looking for Statistical Programmer using R on clinical studies: Key Responsibilities Develop and maintain... ...with programming clinical trial data using R and SAS, and familiarity with CDISC ADaM and SDTM standards Strong...SASRemote job
- Overview Job Summary: We are seeking a skilled Software Developer with a strong background in SAS to join our dynamic team at BASF in Florham Park, NJ. The ideal candidate will have 5 7 years of experience in software development, with a proven track record of delivering...SASPermanent employmentContract workLocal area
$110.88k - $210.6k
...Create/update/run JCL jobs to support security changes and monitoring Analyze data and write reports using RACFRW, ETF/A, zSecure, VRA, SAS, etc. Develop scripts using REXX, Clist, CARLa Manage Problem and Change tickets using IPC tools Present security concepts to...SASMinimum wageFull timePart timeLocal area$124k - $280k
...experience in the consulting industry - Experience leading teams and complex engagements - Demonstrating proficiency in Python, SAS, R, SQL Learn more about how we work: PwC does not intend to hire experienced or entry level job seekers who will need, now or...SASFull timeH1b- ...Job Description This position has a key role to assist the global clinical development, regulatory, and safety to continually assess and... ...Proficient in Microsoft Word, Excel, PowerPoint; EDC databases, SAS datasets Additional Information All your information will be kept...SASLocal area
- ...companies reach further and achieve more with their technology solutions, financial, risk & compliance, and advisory solutions, and clinical solutions. With offices from coast to coast and throughout Europe, Eliassen provides a local community presence, balanced with...Hourly payLocal area
Eliassen Group
Jersey City, NJ27 days ago $135k - $180k
...Company policy. About our Company: Medidata is powering smarter treatments and healthier people through digital solutions to support clinical trials. Celebrating 25 years of ground-breaking technological innovation across more than 36,000 trials and 11 million patients,...Ongoing contractWork at officeLocal areaFlexible hours$90k - $105k
...development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Scope: The Lead Facility Engineer serves as the primary technical subject...Full timeFor contractorsGenScript/ProBio
Piscataway, NJ7 days ago- Please respond back with your resume at "arun at ittblazers dot com" Title R Programmer Duration 6+ Months Contract Role Summary ‘R’ resource will be working on ‘R’ & ‘Python’ platform Governance activities and Code Reviews. Will act as an SME who should be able to administer...Contract work
$137.44k - $167.98k
...professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided by empathy, insight, and clinical intelligence, we collaborate with the best minds in healthcare to address our customers’ toughest challenges. While we continue...Work experience placementH1bRemote workRelocation packageFlexible hoursSolventum
Brooklyn, NY13 hours ago
