Statistical programmer h1.location_city

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Statistical programmer • usa

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Principal Statistical Programmer

Katalyst HealthCares & Life SciencesEdison, NJ

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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...[internal_linking.show_more]

Senior Statistical Programmer (Remote)

Everest Clinical Research Services IncBridgewater, New Jersey, USA

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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...[internal_linking.show_more]

Lead Statistical Programmer

J&J Family of CompaniesWest Chester, PA, United States

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At Johnson & Johnson,?we believe health is everything.Our strength in healthcare innovation empowers us to build a?world where complex diseases are prevented, treated, and cured,?where treatments a...[internal_linking.show_more]

Statistical Programmer

KaztronixMiami, FL, US

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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 ...[internal_linking.show_more]

Statistical Programmer Analyst

F. Hoffmann-La Roche LtdPleasanton, CA, United States

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At Roche you can show up as yourself, embraced for the unique qualities you bring.Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted ...[internal_linking.show_more]

Statistical Programmer

Katalyst HealthCares & Life SciencesTampa, FL

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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 ...[internal_linking.show_more]

Senior Statistical Programmer

EDETEKUS

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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...[internal_linking.show_more]

Principal Statistical Programmer

Katalyst HealthCares & Life SciencesSalt Lake, UT

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Principal Statistical Programmer

Regeneron PharmaceuticalsWarren, NJ, United States

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A principal statistical programmer provides timely support to the study team on all programming matters according to the project strategies.In this role, a typical day might include:.As an integral...[internal_linking.show_more]

Statistical Programmer

Katalyst Healthcares and Life SciencesFernandina Beach, FL, United States

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Our client, a leading Life Sciences Company, needs to hire a Statistical Programmer to provide programming support for Phase 1 to Phase 3 studies, including project integration and disease monitori...[internal_linking.show_more]

Principal Statistical Programmer

AlnylamCambridge, MA, United States

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Principal Statistical Programmer.The Principal Statistical Programmer will provide expert-level hands-on principal programming support and technical leadership to develop, maintain, validate and ru...[internal_linking.show_more]

Statistical Programmer

Katalyst HealthCares & Life SciencesNorth Chicago, IL

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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...[internal_linking.show_more]

Statistical Programmer

PharmaronFranklin Twp, NJ, United States

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Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life.With over 21,000 employees worldwide across 23 locations in the US, UK an...[internal_linking.show_more]

Statistical Programmer Consultant

The Steely GroupRemote, CA, US

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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...[internal_linking.show_more]

Statistical Programmer/Sr. Statistical Programmer

Arrowhead PharmaceuticalsPasadena, California, United States

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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...[internal_linking.show_more]

Junior Statistical Programmer

Cancer Trials IrelandUS

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Key Requirements1.Third level degree in Statistics / Biomedical/Computer Science or related discipline.Experience in SAS or equivalent programming language (eg: R, SPSS).Excellent organisational, c...[internal_linking.show_more]

Statistical Programmer II

ICON Clinical ResearchUnited States

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ICON plc is a world-leading healthcare intelligence and clinical research organization.We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join u...[internal_linking.show_more]

Statistical Programmer Analyst

Experis/Manpower GroupLos Angeles, CA, United States

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Statistical Programmer Analyst/ Data Analyst II.Statistical Programmer Analyst/.We are seeking a Data Analyst II to join one of our leading healthcare clients.This role supports real-world evidence...[internal_linking.show_more]

Principal Statistical Programmer

Katalyst HealthCares & Life SciencesEdison, NJ

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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.