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Statistical programmer • usa

Última actualización: hace 3 días

Senior Principal Statistical Programmer

Katalyst HealthCares & Life SciencesNewark, NJ
A tiempo completo

The Senior Manager in Statistics responsible for perform statistical activities in clinical trials from protocol development to final study report and statistical activities in drug in-licensing, r...Mostrar más

Principal Statistical Programmer (Pharmacometrics)

Regeneron Pharmaceuticals, IncTARRYTOWN
A tiempo completo

A Principal Pharmacometrics Programmer provides timely support to study teams on all programming matters according to project strategies.Their responsibilities include creating initial Tables, Figu...Mostrar más

Automation Programmer/SCADA Programmer/PLC Programmer

Keystone Clearwater SolutionsCanonsburg, PA, US
A tiempo completo
Quick Apply

The Automation Programmer is responsible for maintaining and updating Keystone Clearwater Solutions’ automated assets, web-based programs, network infrastructure, SCADA, and PLC systems.This role w...Mostrar más

Statistical Programmer

Katalyst HealthCares & Life SciencesCincinnati, OH
A tiempo completo

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 ...Mostrar más

Statistical Programmer

KaztronixMiami, FL, US
A tiempo completo
Quick Apply

The role of Statistical Programmer is to perform statistical programming activities for all assigned clinical studies sponsored by company.Provide statistical programming expertise with respect to ...Mostrar más

Sr. Statistical Programmer

Katalyst HealthCares & Life SciencesBoulder, CO
Temporal

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 ta...Mostrar más

Senior Statistical Programmer

EDETEKUS
Teletrabajo
A tiempo completo
Quick Apply

Edetek is seeking a highly skilled Senior Statistical Programmer to join our dynamic team.As a leader in data analytics, we are dedicated to providing innovative solutions to our clients in the pha...Mostrar más

Lead Statistical Programmer - Global Studies (Remote)

Penfield Search PartnersFairfield, CT, US
Teletrabajo
A tiempo completo
Quick Apply

Contact: Neisha Camacho/Terra Parsons -.We are seeking a highly experienced Statistical Programmer to lead programming activities across global clinical studies.This role operates beyond executiona...Mostrar más

Programmer Analyst

InsideHigherEdLancaster, California, United States
A tiempo completo +1

Deadline: 4/28/2026 11:59 PM Pacific.Full job description and OFFICIAL application available ONLY at: https://www.Under the direction of the Manager, Enterprise Applications & Development, incumben...Mostrar más

 • Oferta promocionada

Statistical Researcher

AIR WORLDWIDE CORPORATIONBoston, MA, US
A tiempo completo

Join Verisk's Extreme Event Solutions and become part of a growing Research and Modeling Department that sits at the intersection of statistics, data, and real-world catastrophe risk.As a Statistic...Mostrar más

Statistical Programmer Lead

Tata Consultancy ServicesEnglewood Cliffs, NJ
A tiempo completo

Good hold on the TAUG’s andrelated guidelines.Hands on experience in implementing SDTM/ADAM conceptsacross TA’s and various phases of clinical trains.Good understanding onprevious versions on SDTM/...Mostrar más

Senior Statistical Programmer - Remote (US)

MMSCanton, MI, US
Teletrabajo
A tiempo completo
Quick Apply

About MMS Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research ...Mostrar más

Programmer

vTech SolutionSouth Carolina, United States
A tiempo completo

The Lead Power BI Dashboard Developer will support enterprise-wide data visualization initiatives.This role involves designing and developing advanced dashboards, mentoring junior developers, build...Mostrar más

Statistical Programmer

Katalyst HealthCares & Life SciencesNorth Chicago, IL
A tiempo completo

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 Manager...Mostrar más

Statistical Programmer Consultant

The Steely GroupRemote, CA, US
Teletrabajo
A tiempo completo
Quick Apply

Our client is looking to add a Statistical Programmer Consultant to their team on a contract basis.Involved in the programming activities on multiple projects/ studies across various therapeutic ar...Mostrar más

Statistical Programmer/Sr. Statistical Programmer

Arrowhead PharmaceuticalsPasadena, California, United States
A tiempo completo

Arrowhead Pharmaceuticals, Inc.Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them.Using a bro...Mostrar más

Statistical Programmer

R&D PartnersCalifornia, CA
A tiempo completo

R&D Partners is seeking to hire a remote-US.Your main responsibilities as a.Lead the statistical design and analysis of projects, collaborating closely with cross-functional teams, to establish the...Mostrar más

Statistical Processor

eClercxSudbury, MA, United States
A tiempo completo

Manages the integrity of pricing data in SAP for assigned regional area.Manages import pricing for assigned regional areas.Researches, evaluates, and calculates the client's price information for a...Mostrar más

Senior Principal Statistical Programmer

Senior Principal Statistical Programmer

Katalyst HealthCares & Life SciencesNewark, NJ
Hace 19 días
Tipo de contrato
  • A tiempo completo
Descripción del trabajo

Job Description:
The Senior Manager in Statistics responsible for perform statistical activities in clinical trials from protocol development to final study report and statistical activities in drug in-licensing, regulatory filings and marketing.
Responsibilities:
  • Review protocol, understand study requirements, prepare statistical sections, design study elements including sample size calculation, analysis methods, study duration, etc.
  • Review CRF, database design, and edit check specs.
  • Review study quality surveillance plan and monitor study conduct.
  • Prepare and/or review SAP, TFL shells and specifications for variable derivation.
  • Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables.
  • Provide statistical and validation support for statistical analysis, analysis datasets and TFL.
  • Review study report, manuscripts and other documents related to statistics.
  • Work on responses to health authorities and execute new analysis required for responses, review statistical inputs for regulatory documents.
  • Perform other ad-hoc statistical activities as needed.
  • Works effectively with cross functional groups, study team, and vendors. Proactively control and monitor timelines related to statistics and statistical programming.
  • Participates in monitoring CRO activities and reviewing CRO deliverables Other duties as assigned.
Requirements:
  • or MS in Statistics or Biostatistics.
  • Minimum of years (Ph. D) or years (MS) Pharmaceutical/CRO industry experience.
  • Excellent knowledge of SAS computer package.
  • Excellent knowledge of industry standards, such as the ICH guidelines, CDISC data structures and FDA guidelines.
  • Excellent organizational skills, time management, and ability to meet established deadlines.
  • Excellent communication and interpersonal skills to effectively interface with others.
  • Ability to work independently and problem-solve.
  • Ability to provide leadership for the CRO statisticians and statistical programmers.