Biostatistician Job at Chickasaw Nation Industries, Inc (CNI)

Senior Biostatistician

Job opportunity for a permanent, onsite Senior Biostatistician role in Paris, Fr...

Location

France , Paris

Salary:

Not provided

AB SCIENCE

Expiration Date

Until further notice

Requirements

Ph.D. in Statistics with minimum 3 years of relevant pharmaceutical (or CRO) industry work experience or Masters in Statistics or equivalent with minimum 5 relevant pharmaceutical (or CRO) industry work experience
Good Knowledge of SAS
Good Understanding of CDISC Concepts
Good understanding of ICH guidelines
Fluent in English

Job Responsibility

Author the Statistical Sections of Protocol
Propose and Review the Study design
Calculate the sample size
Review the Case Report Form (CRF)
Review the Edit Check Document (specifically for critical modules like RECIST 1.1 etc.)
Write the randomization specifications and coordinate and finalize all the randomization activities with the IWRS vendor
Author Statistical Analysis Plan (interim and final as appropriate)
Perform the Statistical Analysis (Efficacy and Safety (key safety like Adverse Events)) using SAS
Ensure quality of all the outputs developed
Perform the role of validator as appropriate

What we offer

Permanent position
Salary & package to define according skills and experience

Fulltime

Biostatistician

Part-Time (0.6FTE) | 12-Month Contract. At the South Australian Health and Medic...

Location

Australia , Adelaide

Salary:

Not provided

SAHMRI

Expiration Date

February 01, 2026

Requirements

Honours degree in statistics, biostatistics, or mathematics
Strong understanding of biostatistics concepts, clinical design, and the theory of statistical modelling
Experience in statistical analysis of research data (particularly survival, linear mixed models and analysis of longitudinal data)
Experience in SAS or R programming
Excellent written and verbal communication skills, with the ability to explain statistical results clearly
Experience working with large-scale health-related observational databases
Understanding of data management and cleaning principles for clinical research
Strong relationship-building skills and ability to work effectively in a team
High attention to detail and strong organizational and time management skills

Job Responsibility

Managing registry data and preparing routine reports
Contributing to research projects and clinical studies
Contributing to the design, development, and applyication of statistical methods
Collaborating with multidisciplinary teams including Clinicians, Researchers, Biostatisticians and Data managers
Assisting with the preparation of reports and manuscripts for publication
Staying up to date with emerging statistical methodologies
Driving process improvements through special projects

What we offer

salary packaging options up to $15,900

Parttime

New

Senior Biostatistician

Beacon Biosignals is seeking an experienced data scientist/biostatistician to he...

Location

United States , Boston

Salary:

Not provided

Beacon Biosignals

Expiration Date

Until further notice

Requirements

Multiple years in industry using expertise in (frequentist) biostatistics to design and analyze clinical trials
Deep familiarity with statistical modeling, including interpretation and diagnostics
Substantial experience presenting analyses to external audiences of varied backgrounds
Experience in a fast-paced, highly customer-facing environment
Experience writing and reviewing code in a shared, version-controlled codebase with multiple contributors and users
Experience with thoughtful data curation
Excellent written and verbal communication and listening skills
Ability to stay calm and organized to meet tight deadlines amidst ambiguity
Familiarity with and/or excitement to work with Julia, AWS, Superset, Pandoc, SQL, and GraphQL
Exceptional attention to detail and a high standard of quality

Job Responsibility

Lead and support the development of statistical analysis plans for clinical trials
Perform power and sample size calculations
Deliver clear and impactful presentations and data visualizations to varied audiences
Lead and support the scientific and technical aspects of multiple concurrent studies, including timeline estimation, task delegation, timely execution, and stakeholder communication
Engage with external stakeholders to align their needs with internal capabilities
Contribute to group-level processes and procedures
Co-author scientific reports
Write and review reusable, documented, tested code
Leverage Beacon's products and subject matter expertise to inform analysis planning and execution
Dig into large, messy, unfamiliar datasets, document their idiosyncrasies and provenance, and harmonize them with Beacon's datastore

What we offer

Equity
PTO

New

Senior Statistical Programmer II

Statistical Programmer II, Canada, Remote. ICON plc is a world-leading healthcar...

Location

Canada , Montreal

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, or a related field
Significant experience in statistical programming within the clinical research or pharmaceutical industry
Strong proficiency in SAS programming and a solid understanding of statistical concepts and methodologies
Excellent analytical skills, attention to detail, and the ability to manage multiple projects simultaneously
Strong communication and interpersonal skills, with the ability to work collaboratively within a multidisciplinary team

Job Responsibility

Designing, developing, and validating SAS programs/R-Shiny applications for statistical analysis and reporting of clinical trial data
Working closely with biostatisticians to create comprehensive analysis plans and apply appropriate statistical methods
Performing quality control checks and reviewing statistical outputs to ensure compliance with project specifications and regulatory guidelines
Assisting in the preparation of statistical reports, presentations, and regulatory submissions to support clinical development programs
Mentoring junior programmers and contributing to team development by sharing best practices and technical knowledge

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

New

Senior Manager, Biostatistician Consultant

As a member of Parexel’s Biostatistics group, your expertise in statistical meth...

Location

Argentina

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

PhD or MS in Statistics or related discipline with substantial experience
Good analytical skills
Good project management skills
Professional attitude
Attention to detail
Thorough understanding of statistical issues in clinical trials
Ability to clearly describe advanced statistical techniques and interpret results
Familiarity with regulatory/research guidelines on drug development, GCP, and statistical principles (especially ICH guidelines)
Prior experience with SAS programming required
Ability to work independently

Job Responsibility

Provide broad statistical support, including trial design, protocol and CRF development on specific studies
Lead production and quality control of randomization, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents
Perform sample-size calculations, generate randomization lists and write statistical methodology sections for inclusion in study protocols
Provide statistical input into Data Monitoring Committee (DMC) activities, including development of DMC charters and analysis plans
Provide a supporting role as a non-voting independent statistician providing data and analysis for DMC review
Support of Business Development, by actively contributing to study design considerations in internal and client meetings, providing and discussing sample size scenarios, support of budget and proposal development, attending and preparing bid defense meetings
Understand regulatory requirements related to the specific therapeutic areas and the implications for statistical processing and analysis
Understand, apply and provide training in extremely advanced and sometimes novel statistical methods
Contribute to the development and delivery of internal and external statistical training seminars and courses
Review position papers based on current good statistical practice

What we offer

Patient-led in everything we do
Supportive and inclusive environment
Opportunities for career growth
Flexible work arrangements
Diverse therapeutic areas and project exposure
Advanced Technology

Biostatistician II

As a member of Parexel’s Biostatistics group, your expertise in statistical meth...

Location

Taiwan

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

PhD in Statistics or related discipline entry level, MS in Statistics or related discipline with some experience
Good analytical skills
Good project management skills
Professional attitude
Attention to detail
A good understanding of statistical issues in clinical trials
Prior experience with SAS programming desirable
Ability to work independently
Good mentoring/leadership skills
Competent in written and oral English in addition to local language

Job Responsibility

Production and/or QC of derived datasets and both simple and advanced statistical outputs using efficient programming techniques
Understand and apply moderately advanced statistical methods
Coordinate and lead a project team to successful completion of a project within given timelines and budget
Interact with clients as key contact with regard to statistical and contractual issues
Assist in the production of analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents
Check own work in an ongoing manner to ensure first-time quality
Provide training in statistical analysis to internal clients
Proactively participate in and/or lead process/quality improvement initiatives
Travel to, attend and actively contribute to all kind of client meetings as appropriate
Mentor and train junior members of the department

What we offer

Patient-led in everything we do
Supportive and inclusive environment
Opportunities for career growth
Flexible work arrangements
Diverse therapeutic areas and project exposure
Advanced Technology

Senior Statistical Programmer

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

United Kingdom , Reading

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, or a related field
Significant experience in statistical programming within the clinical research or pharmaceutical industry
Strong proficiency in SAS programming and a solid understanding of statistical concepts and methodologies
Excellent analytical skills, attention to detail, and the ability to manage multiple projects simultaneously
Strong communication and interpersonal skills, with the ability to work collaboratively within a multidisciplinary team

Job Responsibility

Designing, developing, and validating SAS programs for statistical analysis and reporting of clinical trial data
Working closely with biostatisticians to create comprehensive analysis plans and apply appropriate statistical methods
Performing quality control checks and reviewing statistical outputs to ensure compliance with project specifications and regulatory guidelines
Assisting in the preparation of statistical reports, presentations, and regulatory submissions to support clinical development programs
Mentoring junior programmers and contributing to team development by sharing best practices and technical knowledge

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Biostatistician

The Biostatistician is responsible for designing, conducting, and analyzing stat...

Location

Salary:

Not provided

KGTiger

Expiration Date

Until further notice

Requirements

Bachelor’s degree in biostatistics, statistics, mathematics, or a related field
Experience in biostatistics
Strong programming skills
Experience with statistical analysis software
Excellent communication and problem-solving skills.
Strong understanding of statistical concepts
Excellent problem-solving and analytical skills
Excellent written and verbal communication skills
Ability to work independently and as part of a team
Experience with statistical software

Job Responsibility

Design and conduct statistical studies.
Interpret and communicate statistical results.
Develop statistical methods.
Collaborate with researchers.
Stay up-to-date on the latest statistical methods.

Biostatistician

Chickasaw Nation Industries, Inc (CNI)

Location:
United States

Category:
IT - Software Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 22, 2026

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