Biostatistician Job at Proclinical (Detroit)

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

The Biostatistician requires frequent interaction with leadership, scientists, e...

Location

United States

Salary:

145000.00 - 150000.00 USD / Year

Chickasaw Nation Industries, Inc (CNI)

Expiration Date

Until further notice

Requirements

Must be able to obtain and maintain the required customer clearance for access to systems, facilities, equipment and property
CDC / health / science experience is strongly preferred
MS/MPH/MBA or similar degree and a minimum of ten (10) years of experience working in communications project management and communications department management

Job Responsibility

Design, test, and produce high-quality data collection tools and survey instruments
Develop, clean, document, and maintain secure, structured databases using CDC-approved platforms
Perform advanced statistical data analyses on complex public health and clinical datasets
Conduct systematic literature reviews and evidence synthesis
Collaborate closely with the client’s internal teams and external partners
Provide statistical consultation on study design, sample size calculations, weighting methodologies, and adjustment for bias
Assist in the preparation and authorship of abstracts, peer-reviewed journal articles, scientific reports, and presentations
Prepare clear, publication-ready tables, figures, and visualizations
Deliver all products on time, with documented code, reproducible results, and full compliance with CDC information quality guidelines and federal regulations

What we offer

Medical
Dental
Vision
401(k)
Family Planning/Fertility Assistance
STD/LTD/Basic Life/AD&D
Legal-Aid Program
Employee Assistance Program (EAP)
Paid Time Off (PTO) – (11) Federal Holidays
Training and Development Opportunities

Fulltime

Biostatistician

The Biostatistician requires frequent interaction with leadership, scientists, e...

Location

United States

Salary:

100000.00 - 120000.00 USD / Year

Chickasaw Nation Industries, Inc (CNI)

Expiration Date

Until further notice

Requirements

Must be able to obtain and maintain the required customer clearance for access to systems, facilities, equipment and property
CDC / health / science experience is strongly preferred
MS/MPH/MBA or similar degree and a minimum of ten (10) years of experience working in communications project management and communications department management

Job Responsibility

Design, test, and produce high-quality data collection tools and survey instruments
Develop, clean, document, and maintain secure, structured databases using CDC-approved platforms
Perform advanced statistical data analyses on complex public health and clinical datasets
Conduct systematic literature reviews and evidence synthesis
Collaborate closely with the client’s internal teams and external partners
Provide statistical consultation on study design, sample size calculations, weighting methodologies, and adjustment for bias
Assist in the preparation and authorship of abstracts, peer-reviewed journal articles, scientific reports, and presentations
Prepare clear, publication-ready tables, figures, and visualizations
Deliver all products on time, with documented code, reproducible results, and full compliance with CDC information quality guidelines and federal regulations

What we offer

Medical
Dental
Vision
401(k)
Family Planning/Fertility Assistance
STD/LTD/Basic Life/AD&D
Legal-Aid Program
Employee Assistance Program (EAP)
Paid Time Off (PTO) – (11) Federal Holidays
Training and Development Opportunities

Fulltime

New

Senior Biostatistician

We are seeking a skilled and motivated Senior Biostatistician to join our fast-m...

Location

United States

Salary:

120000.00 - 160000.00 USD / Year

canfield scientific

Expiration Date

Until further notice

Requirements

Master's degree in Biostatistics, Statistics, Mathematics or closely related quantitative discipline with at least 4 years of clinical research within a regulated environment (pharmaceutical, biotechnology, CRO, or medical device industry) or PhD with at least 2 years of relevant experience
Demonstrated experience independently authoring Statistical Analysis Plans (SAPs), contributing to clinical study reports and regulatory documentation
Proficiency in SAS, including validated code development, QC, and production of regulatory-grade TLFs
Solid understanding of statistical methodology for clinical trials, including analysis population definitions, endpoint types, missing data, and multiplicity considerations
Ability to communicate statistical results within the clinical study context
Working knowledge of ICH E9/E9(R1) and FDA regulatory expectations
Strong analytical skills with high attention to data integrity, reproducibility, and traceability
Ability to manage projects or analysis within established timelines
Experience with medical imaging or dermatology clinical studies
Exposure to regulatory submission processes

Job Responsibility

Independently author Statistical Analysis Plans (SAPs), including definition of analysis populations, endpoints, statistical methods, missing data handling, and sensitivity analyses
Provide statistical input into study protocols, including endpoint definition, sample size considerations, and methodological recommendations
Develop, validate, and maintain SAS programs for analysis datasets, tables, listings, and figures (TLFs) in accordance with SAPs
Perform statistical analyses aligned with SAPs and study objectives, ensuring accuracy, reproducibility, and compliance with regulatory expectations
Prepare statistical sections of clinical study reports (CSRs), including interpretation of results
Ensure analyses adhere to ICH and FDA guidance
Collaborate cross-functionally with clinical, regulatory, data management, and medical writing teams to support study deliverables

What we offer

Paid days off
Medical insurance
Dental insurance
Vision insurance
Discretionary bonus
401(k) plan with employer match

Fulltime

Senior Principal Biostatistician

We are currently seeking a Senior Principal Biosttistician to join our diverse a...

Location

United States , Blue Bell

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

A master's degree or Ph.D. in Biostatistics, Statistics, or a related field
Extensive experience in biostatistics within the pharmaceutical or biotech industry, particularly in clinical trial design and analysis
Strong knowledge of statistical software (e.g., SAS, R) and proficiency in programming for data analysis
Excellent problem-solving skills, with the ability to interpret complex data and provide actionable insights
Demonstrated leadership abilities, with experience in mentoring and guiding teams
Strong communication skills, with the ability to present statistical concepts to non-statistical audiences effectively
Detail-oriented, with excellent organizational skills to manage multiple projects and meet deadlines in a fast-paced environment

Job Responsibility

Designing and implementing statistical analysis plans for clinical trials, ensuring alignment with study objectives and regulatory guidelines
Overseeing the statistical analysis of clinical data, providing insights and interpretations to support decision-making and reporting
Collaborating with cross-functional teams, including clinical, regulatory, and data management, to ensure integrated and efficient study execution
Mentoring junior statisticians and providing training on statistical methodologies and software applications
Contributing to the preparation of regulatory submissions and publications, ensuring statistical rigor and transparency
Staying updated on industry trends and advancements in statistical methodologies to drive innovation in study design and analysis
Participating in protocol development and providing input on endpoints and statistical considerations for clinical studies

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

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

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 with some experience or MS in Statistics or related discipline with significant experience
Good analytical skills
Good project management skills
Professional attitude
Attention to detail
Thorough understanding of statistical issues in clinical trials
Prior experience with SAS programming required
Ability to work independently
Good leadership skills
Good business awareness/ business development

Job Responsibility

Coordinate and lead a project team to successful completion of a project within timelines and budget
Interact with clients as key contact with regard to statistical and contractual issues
Perform QC of derived datasets, tables, figures and data listings produced by other members of the department
Check own work in an ongoing way to ensure first time quality
Understand and apply advanced statistical methods
Lead production and quality control of randomizations, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents
Provide a supporting role as a non-voting independent statistician providing data and analysis for DMC review
Travel to, attend, and actively contribute to all kind of client meetings as appropriate (e.g. discussing analysis concepts, presenting, discussing and interpreting study results)
Support of Business Development, e.g. 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 for potential studies, programs of work and FSPs

What we offer

Flexible, supportive, and inclusive working environment
Opportunities for career growth
Flexible work arrangements
Diverse therapeutic areas and project exposure
Advanced Technology
Training programs, mentoring, and knowledge sharing

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

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