Biostatistician II Job at Parexel

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 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 Biostatistician II

The Clinical Biostatistician II, with general guidance from more experienced Sta...

Location

United States , Madison

Salary:

88000.00 - 133200.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

Master’s degree in Biostatistics or field as outlined in the essential duties
or Bachelor's degree in Biostatistics or field as outlined in the essential duties, plus 2 years of experience in lieu of a Master’s degree
4+ years of relevant work experience, as outlined in the essential duties
Demonstrated statistical experience in molecular diagnostic, drug, or medical device development
epidemiology
public health
or healthcare
Professional working knowledge of theoretical and applied statistics
Strong statistical programming skills (SAS, R, or Python)
Strong verbal, written, and graphical communication/presentation skills

Job Responsibility

Design clinical validity, clinical utility, health economics, and clinical experience studies
Evaluate evidentiary requirements
Contribute to proposals, FDA pre-submissions, and study protocols (selecting endpoints, power and sample size calculations, and analysis plans)
Review case report forms and data transfer requirements
Author statistical analysis plans
Apply rigorous statistical methodology and programming to: Monitor clinical data quality
Develop evidence for clinical predictive models in clinical studies and trials
Conduct simulation studies
Communicate statistical results in tables, figures, and listings
statistical analysis reports

What we offer

Paid time off (including days for vacation, holidays, volunteering, and personal time)
Paid leave for parents and caregivers
A retirement savings plan
Wellness support
Health benefits including medical, prescription drug, dental, and vision coverage
Bonus eligibility

Fulltime

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

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

Software Developer

Work with the IT development team to design and develop our internal and client-...

Location

Cyprus , Nicosia

Salary:

Not provided

Albourne

Expiration Date

Until further notice

Requirements

A degree in Computer Science or a science degree with programming experience or equivalent practical experience
Strong organizational and time management skills
Strong ability to multi-task and set priorities
Strong programming skills
Good knowledge of Java
Working in teams with other developers, business analysts, business users in an international environment
Travel
Work outside of normal business hours – coinciding with systems releases or urgent bug fixes
Abide by the Communication Group policies and procedures as well as the Albourne Group's policies and procedures, including but not limited to compliance reporting, HFDB filing, Information, Communications & Cyber Security Policy, Expense & Travel Policy etc.
Comply with terms of Albourne Compliance Manuals

Job Responsibility

Designing and developing software in cooperation with business users
Apply advanced software engineering techniques to support CI and weekly releases
Observing a test-driven development process
Accurately estimating required development time
Refactoring existing code to improve security, maintainability, efficiency, resilience and the user experience
Pro-actively seek to improve efficiencies, user experience, maintainability and resilience
Stay abreast of new technological and design developments

What we offer

Fully paid Medical and Dental Insurance for you and your dependents
Employee Assistance Program (EAP)
Provident Fund Contribution
Career growth and tools for ongoing learning and development
Annual bonus dependent upon performance and company growth
5 additional service recognition holidays in surplus to standard annual leave after 5 years of service
Albourne Training Days
Free office parking

Fulltime

Support Worker

Are you passionate about making a genuine difference in a young person's life? W...

Location

United Kingdom , Harrow

Salary:

13.00 - 17.35 GBP / Hour

Randstad

Expiration Date

July 25, 2026

Requirements

Resilient, patient, and empathetic nature with a passion for supporting young people
Excellent communication skills and the ability to handle challenging situations calmly
Prior experience in health and social care, youth work, or supported living is a plus, but a great attitude and values-driven approach are most important

Job Responsibility

Prioritise Safety & Wellbeing
Build Independence
Support Pathways
Be a Trusted Adult

What we offer

Dedicated Consultants with experience in education
Recommend a friend bonus worth up to £300
online training
DBS and application support
Free parking

Fulltime

Test Technician I

The Test Technician I is responsible for ensuring the tested circuit boards and ...

Location

United States , Tampa

Salary:

Not provided

Sypris Electronics

Expiration Date

Until further notice

Requirements

Associates degree in electronic technology or equivalent combination of education and experience
Minimum of one year electronics technology experience
Good computer skills, ability to follow detailed program instructions
Working knowledge of oscilloscope, voltmeter, toneohm and RCL meter
Must be able to read/interpret schematics
Requires a mixture of standing and sitting
May require handling of or exposure to chemicals used in the assembly process
May require occasional lifting of up to 35 pounds
Good oral and written communication skills

Job Responsibility

Tests boards and assemblies in accordance with instructions, procedures and related program
Troubleshoots failed boards assemblies utilizing complex test equipment and standard troubleshooting techniques
Resolves new and difficult problems independently
Records results of tests and troubleshooting on data sheets
Upon detecting deviations with regard to test equipment, test procedures and/or repetitive failures, determines if station, board, assembly or fixture problem
Notifies supervisor of deviation regarding test equipment, test procedures or repetitive failures

What we offer

health
dental
vision
life
disability
401(k) with company matching
9/80 work schedule

Fulltime

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Biostatistician II

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