Biostatistician Job at Proclinical (Detroit)

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

New

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.

Biostatistician IV

This position will be part of the Real-World Advocate DAta for Research (RADAR) ...

Location

United States , Winston Salem

Salary:

47.50 - 71.25 USD / Hour

Advocate Health Care

Expiration Date

Until further notice

Requirements

Master's degree in Biostatistics or Statistics or health-related field (e.g., Health Informatics, Epidemiology, Public Health) with seven years' experience in statistics
Experience in analyzing data using statistical package(s) and working with large datasets and databases required
Experience working with health-related data (e.g., EHR data, claims, registries, vital statistics) and healthcare/pharmaceutical environments preferred
Strong programming skills in R (including R Markdown, Python, and Shiny) and familiarity with Git for version control
Proven experience working with large datasets and databases (SQL proficiency and Snowflake experience desirable)
Ability to organize workflows, manage projects, and collaborate effectively in team settings

Job Responsibility

Collaborates independently or as co-investigator with other investigators and project teams to develop objectives and data collection procedures to achieve objectives
Assumes major responsibilities on research projects (e.g., Assisting in creating and maintaining registries and project databases/documentation, develop efficient workflows for data collection including directing data extractions, cleaning, and integration)
Assumes leadership responsibilities on working groups, and research project teams including directing and/or supervising project personnel and coordinating quality control efforts
Designs analyses and report generation procedures for specific research studies or registries and writes statistical methods, data documentation, and results sections of reports and publications
Develops statistical design and planned analyses for proposals and takes primary responsibility for statistical/methodological design
Applies for specific extramural grants and pharmaceutical contracts
Prepares scientific manuscripts, abstracts, white papers, and documentation for longitudinal datasets
Makes oral presentations at internal/professional/scientific meetings, workshops, and seminar series
Supervises the work of Biostatisticians I, II, III and Analyst/Programmers serving on the same projects
Performs other related duties incidental to the work described herein

What we offer

Paid Time Off programs
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
Flexible Spending Accounts for eligible health care and dependent care expenses
Family benefits such as adoption assistance and paid parental leave
Defined contribution retirement plans with employer match and other financial wellness programs
Educational Assistance Program
Premium pay such as shift, on call, and more based on a teammate's job
Incentive pay for select positions
Opportunity for annual increases based on performance

Fulltime

New

Senior Clinical Data Science Programmer

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

Location

Mexico , Mexico City

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Advanced degree in a relevant field such as computer science, statistics, or life sciences
Extensive experience in programming for clinical trials, with proficiency in languages such as SAS, R, or Python
Strong problem-solving skills and the ability to work collaboratively in a fast-paced, cross-functional environment
Excellent attention to detail and organizational skills, with a commitment to delivering high-quality results
Strong communication and interpersonal skills, with the ability to effectively collaborate with diverse teams and influence outcomes

Job Responsibility

Developing, validating, and maintaining programming solutions for data analysis and reporting in clinical trials
Collaborating with clinical data scientists and biostatisticians to ensure the integration of programming solutions into the overall data management process
Overseeing the generation of statistical datasets, tables, listings, and figures to support regulatory submissions and study reports
Providing guidance on programming best practices, coding standards, and data quality control measures
Staying updated on advancements in programming languages and data management tools to enhance operational efficiencies

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

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

Clinical Research Assistant

This Clinical Research Assistant position at Boston Children’s Hospital offers a...

Location

United States , Boston

Salary:

41246.40 - 61339.20 USD / Year

Boston Children's Hospital

Expiration Date

Until further notice

Requirements

Bachelor’s degree in an appropriately related discipline, preferably in a Life, Health, or Social Sciences field
Analytical and statistical skills necessary to gather and interpret data
Well-developed communication skills
Well-developed organizational skills
Advanced writing skills for preparing IRB submissions, writing abstracts, and drafting manuscripts
Willingness to have direct contact with animals on basic science projects
Must be able to work autonomously

Job Responsibility

Manage multiple clinical and basic science research projects at once
Navigate electronic medical record systems (PowerChart and Epic)
Use REDCap Electronic Data Capture service to create databases
Read through patient charts/medical documentation to collect data
Screen, recruit, and obtain informed consent from eligible patients and families
Monitor data collection for quality and HIPAA compliance
Consult with clinical teams as well as research support staff
Participate in collaborative projects and initiatives
Perform basic statistical analysis on data
Work closely with the department’s biostatistician

What we offer

Flexible schedules
Affordable health, vision and dental insurance
Child care and student loan subsidies
Generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement
Cell phone plan discounts
Discounted rates on T-passes

Fulltime

Clinical Affairs Specialist

Clinical Affairs Specialist role at DentalMonitoring, a MedTech scale-up. The ro...

Location

United States , Austin

Salary:

Not provided

DentalMonitoring

Expiration Date

Until further notice

Requirements

Engineering degree, Master’s in Regulatory Affairs, or similar field
2 to 5 years of experience managing clinical studies, from design through dissemination of results
Proficient in GCP/BPC and the regulatory framework applicable to medical devices: MDR 2017/745, ISO 14155, ISO 13485
Structured, methodical, and comfortable in a multi-project environment
Adaptable and motivated by continuous learning
Excellent interpersonal skills and strong communication abilities
Can work autonomously while actively sharing information and contributing to team discussions

Job Responsibility

Lead the design of clinical studies, from needs analysis through protocol writing, in collaboration with R&D, Product, Regulatory, and clinical experts
Design and challenge robust study designs, define statistical plans with biostatisticians, and maintain scientific and methodological watch to integrate best practices
Organize and execute study start-up: site selection and qualification, contracting, coordination of internal and external stakeholders, operational follow-up, and adherence to timelines/budgets
Ensure the proper conduct of studies by overseeing scientific, methodological, and regulatory compliance
Verify the quality, integrity, and completeness of collected data to ensure compliance with the protocol
Analyze and interpret results in collaboration with statisticians
Write study reports and contribute to the scientific valorization of the work (publications)
Contribute to clinical evaluation (CEP, CER) and post-market clinical follow-up (PMCF) in accordance with regulatory requirements
Participate in the company’s clinical strategy by proposing new ideas and conducting medico-economic studies to support product development

What we offer

Medical, Dental, and Vision Insurance
Short-Term & Long-Term Disability
Health Savings Account (HSA) and Flexible Spending Accounts (FSA)
Basic and Supplemental Life Insurance
Accident, Indemnity, and Critical Illness Coverage
401(k) Retirement Plan
Paid Time Off (PTO) and Company Holidays

Fulltime

Sr. Research Prog Specialist

The Senior Department Program Specialist - SHORE will collaborate with the Direc...

Location

United States of America , Rochester

Salary:

60431.00 - 84603.00 USD / Year

University of Rochester

Expiration Date

Until further notice

Requirements

Bachelor's degree required
Master degree, Advanced degree (PhD or MD) preferred
5 years of relevant experience required
Prior experience in higher education, academic research and grants administration preferred
Strong leadership and team management skills
Exceptional communication, negotiation, and relationship-building skills
Proficiency in program evaluation and data analysis
Strong project management skills, with the ability to manage multiple tasks simultaneously
Strong organizational skills, attention to detail and problem-solving ability.
Advanced budget management and financial planning expertise

Job Responsibility

Provide leadership and oversight for SHORE research projects, supporting faculty and trainees in study design, recruitment, regulatory compliance, and reporting
Lead strategic planning and implementation of complex research programs aligned with departmental priorities in surgical outcomes.
Develop and expand a sustainable, independently funded research portfolio in surgical health outcomes, including federal (e.g., NIH, AHRQ, PCORI) and foundation grants.
Serve as a liaison to the Department of Surgery leadership to integrate outcome-focused initiatives and skill-building across divisions.
Organize and lead meetings, track project progress, and prepare updates and reports for internal stakeholders and funding agencies.
Foster interdisciplinary collaborations across departments and research centers at URMC to maximize institutional impact and minimize siloed efforts.
Oversee regulatory processes, including human subjects protocols and maintenance of study documentation.
Maintains multiple health outcomes databases and is responsible for managing subscriptions, submission, and access for researchers.
Engage and coordinate the investigators including biostatisticians, data analysts, and dissemination experts, to ensure high-quality research outputs.
Establish and track clear performance metrics and outcomes to evaluate SHORE’s impact and guide continuous improvement

Fulltime

Biostatistician

Proclinical

Location:
United States , Detroit

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
March 22, 2026

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

Similar Jobs for Biostatistician

Senior Biostatistician

Biostatistician II

Biostatistician IV

Senior Clinical Data Science Programmer

Biostatistician II

Clinical Research Assistant

Clinical Affairs Specialist

Sr. Research Prog Specialist

Biostatistician

Proclinical

Location:United States , Detroit

Category:Research and Development

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:March 22, 2026

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

Similar Jobs for Biostatistician

Senior Biostatistician

Biostatistician II

Biostatistician IV

Senior Clinical Data Science Programmer

Biostatistician II

Clinical Research Assistant

Clinical Affairs Specialist

Sr. Research Prog Specialist

Location:
United States , Detroit

Category:
Research and Development

Contract Type:
Not provided

Job Posted:
March 22, 2026