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Statistical programmer • usa

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Principal Statistical Programmer

Katalyst HealthCares & Life SciencesEdison, NJ
A tiempo completo

Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs.Be responsible for overall project delivery, including clinical trial reports and other regulator...Mostrar más

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

Senior Statistical Programmer (6-12 Years)

vueverse.Salem, IN
Temporal

Senior Statistical Programmer Experience: 6–12 Years Location: Hyderabad Role Overview The Senior Statistical Programmer will support clinical trial programming activities including SDTM, ADaM data...Mostrar más

Statistical Programmer

Katalyst HealthCares & Life SciencesJacksonville, FL
A tiempo completo

Our client, a leading Life Sciences Company, needs to hire a Statistical Programmer to provide programming support for Phase to Phase studies, including project integration and disease monitoring p...Mostrar más

Sr. Statistical Programmer

Glaukos CorporationUnited States
A tiempo completo

Review key study documents produced by other functions (protocols, statistical analysis plans [SAPs], TFL shells, case report forms) and interact with Statisticians and other clinical team members ...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

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

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

Principal Statistical Programmer

ImmunityBioRemote, US
Teletrabajo
A tiempo completo

A Principal Statistical Programmer is an expert in management, technical oversight, and quality of statistical programming activities related to the analyses of clinical trial data ensuring timelin...Mostrar más

Senior Statistical Programmer - Remote (US)

MMSPhiladelphia, PA, 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

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

Statistical Programmer

Akaasa TechnologiesUnited States
A tiempo completo
Quick Apply

Statistical Programmer 100% Remote A biotech company in North Carolina is seeking a new Statistical Programmer to join their team remotely, developing SAS programming deliverables for clinic...Mostrar más

Programmer

MRA Recruiting ServicesGermantown, WI, US
A tiempo completo
Quick Apply

CNC Machine Programmer (Laser / Punch / Fabrication) KSM Industries Germantown, WI Position Summary The CNC Machine Programmer is responsible for creating, optimizing, and maintaining programs for ...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 Analyst

Horizontal TalentColumbus, OH, US
A tiempo completo

Do you have statistics experience, and are you seeking a new job in Columbus? Horizontal Talent is helping a collaborative company recruit a Statistics Analyst, and the contract role comes with an ...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

Principal Statistical Programmer (Remote)

Everest Clinical Research Services IncBridgewater, New Jersey, USA
Teletrabajo
A tiempo completo

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, biote...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

Principal Statistical Programmer

Principal Statistical Programmer

Katalyst HealthCares & Life SciencesEdison, NJ
Hace más de 30 días
Tipo de contrato
  • A tiempo completo
Descripción del trabajo

Responsibilities:
  • Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs.
  • Be responsible for overall project delivery, including clinical trial reports and other regulatory submission deliverables.
  • 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.
  • Assist in establishing standardized programming procedures and work instructions.
  • Develop, enhance, evaluate, and validate standardized macros and utility programs to ensure that regulatory requirements are met through validation/compliance activities.
  • Develop and maintain clinical processing workflow systems.
  • Assist in the development of client proposal documents.
  • Provide leadership, project specific training, stakeholder management, external sponsor support, resource management, and project management for the required programming tasks supporting clinical trial activities.
  • Provide input into and negotiate statistical programming timelines. Ensure that timelines are adhered to and coordinate and lead a statistical programming team to successful completion of a study within given timelines and budgets.
  • Trained in sponsor SOPs and disseminate knowledge to project team members as appropriate.
  • Provide input into, and mentor statistical programmers to provide input into documents produced by other functions (, biostatisticians, data managers, medical writers, etc.)
  • records handling (, Chapter of the US Code of Federal Regulation – Part ), and electronic submission of clinical data to agencies (, e-CTD guidance and CDISC SDTM and ADaM standards)
  • Assist in updating/writing PROMETRIKA standard operating procedures (SOPs)
  • Develop tools in SAS for data analysis and reporting that comply with regulatory requirements.
  • Develop specifications (, metadata files), annotate CRFs and create SAS programs for the mapping of raw datasets to CDISC SDTM standards.
  • Create files from metadata files for SDTM and ADaM
  • Convert data received in other formats to SAS datasets.
Requirements:
  • Must have expertise in SAS/BASE, SAS/STAT, and knowledge of SAS/CONNECT, SAS/ACCESS, SAS/MACRO, SAS/GRAPH, SQL, and ODS
  • Knowledge of SDTM, ADaM, FDA and ICH guidance
  • Understanding of Code of Federal Regulations (CFR) Title , Part that covers the management of electronic records and electronic signatures in computer systems.
  • Good organizational skills across individual projects and managing own and teamwork loads. Ability to organize, manage and complete multiple assignments with challenging timelines independently and effectively.
  • Consistent experience as a lead statistical programmer on several concurrent projects
  • Strong understanding of drug development, including knowledge of interfaces and interdependencies with other functions
  • Strong mentoring skills as shown by leadership of projects and if applicable, junior team members.
  • Excellent analytical skills
  • Proven ability to learn new systems and function in an evolving technical environment.
  • Ability to negotiate and influence to achieve results.
  • Good presentation skills
  • Good business awareness/business development skills (including financial awareness)
  • Ability to create, maintain and define strategies to improve the efficiency of running a clinical trial.
  • Work effectively in a quality-focused environment.
  • Knowledge of other programming languages and database management software packages is a plus.