Senior Biostatistician Job at Parexel

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 II

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

Location

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Statistics or a related field
Experience in a biostatistics role in the pharmaceutical, clinical research, or healthcare industry is preferred
Proficiency in statistical concepts, study design, sample size calculations, and patient randomization
Familiarity with statistical analysis plans and the design of statistical tables, figures, and data listings for clinical reports
Strong data analysis skills, including data manipulation, retrieval, and interpretation
Proficiency in relevant computer languages and statistical software packages
Ability to write and implement programs to select, retrieve, manipulate, edit, and analyze data
Competency in assisting with statistical analyses and result interpretation
Effective communication and collaboration skills to work with cross-functional teams, including data management personnel, statistical programmers, and clinical research colleagues.

Job Responsibility

Assist senior biostatisticians in clinical study support, including study design, sample size calculations, patient randomization, data analysis, and results reporting
Support the statistical aspects of case report form design
Help in writing statistical analysis plans, defining derived data, and designing statistical tables and figures for clinical summary reports
Write data quality control specifications, utilize relevant computer languages and software
Develop and execute data manipulation and analysis programs
Assist in conducting statistical analyses and interpreting results
Prepare statistical summary reports and contribute to the statistical methods sections of integrated study reports
Review and document analysis and programming work for audit trail purposes
Contribute to project document standards and maintain project-specific biostatistics files
Collaborate effectively with ICON project team members, including data management, statistical programming, and clinical research personnel

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.

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

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

Senior Manager, Biostatistician Consultant

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

Location

United Kingdom

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

PhD in Statistics or related discipline, MS in Statistics or related discipline
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

Flexible work arrangements
Opportunities for career growth
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced Technology

Biostatistician II

We are seeking a skilled and motivated Biostatistician II to join our fast-paced...

Location

United States of America

Salary:

100000.00 - 120000.00 USD / Year

canfield scientific

Expiration Date

Until further notice

Requirements

Master’s degree in Biostatistics, Statistics, Mathematics, or a related quantitative discipline
3–5 years of experience in clinical research within a regulated environment including contributing to Statistical Analysis Plans (SAPs) and drafting sections under senior statistical oversight
Demonstrated proficiency in SAS, including development of validated analysis programs and implementation of standard QC procedures
Solid understanding of statistical methodology for clinical trials, including analysis population definitions, common endpoint types, handling of missing data, and basic multiplicity considerations
Working knowledge of ICH E9/E9(R1) principles and general FDA regulatory expectations
Ability to implement predefined analyses independently and contribute to statistical design discussions with appropriate supervision and manage assigned studies or analysis workstreams within established timelines
Experience contributing to statistical sections of CSRs, TLF specifications, and other regulatory-facing documents

Job Responsibility

Contribute to the development and authoring of Statistical Analysis Plans (SAPs), including drafting key sections (analysis populations, endpoints, missing data handling, sensitivity analyses) under senior statistical guidance
Support protocol development through input on endpoint definitions, statistical methodology, and sample size considerations
Independently develop, validate, and maintain statistical programs for assigned analyses in SAS
Participate in data review activities, and perform data quality checks in collaboration with data management
Perform and interpret statistical analyses aligned with study objectives and regulatory requirements
Draft statistical sections of clinical study reports, TLF shells, and other regulatory-facing documents, with review from senior statisticians
Ensure analyses adhere to ICH and FDA guidance, following established departmental standards and QC procedures
Collaborate cross-functionally with clinical, regulatory, data management, and medical writing teams to support study deliverables
Contribute to process improvement, template development, and standardization initiatives

What we offer

Paid days off
Medical, dental, and vision insurance
May be eligible for a discretionary bonus
401(k) plan with employer match (currently set at 50%)

Fulltime

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

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

Senior Biostatistician

Parexel

Location:
Taiwan

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
April 05, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Senior Biostatistician

Senior Biostatistician

Biostatistician II

Senior Biostatistician

Senior Manager, Biostatistician Consultant

Senior Manager, Biostatistician Consultant

Biostatistician II

Senior Statistical Programmer

Senior Statistical Programmer II

Senior Biostatistician

Parexel

Location:Taiwan

Category:Research and Development

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:April 05, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Senior Biostatistician

Senior Biostatistician

Biostatistician II

Senior Biostatistician

Senior Manager, Biostatistician Consultant

Senior Manager, Biostatistician Consultant

Biostatistician II

Senior Statistical Programmer

Senior Statistical Programmer II

Location:
Taiwan

Category:
Research and Development

Contract Type:
Not provided

Job Posted:
April 05, 2026