Biostatistician II Job at iconplc

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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 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

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

New

Pharmacy Manager

We’re building a world of health around every individual — shaping a more connec...

Location

United States , Hebron

Salary:

65.00 - 85.00 USD / Hour

CVS Health

Expiration Date

April 25, 2026

Requirements

Active Pharmacist License in the state where the Store is located
Active National Provider Identifier (NPI)
Not on the DEA Excluded Parties list
1-2 years of experience as a Pharmacist
Regular and predictable attendance, including nights and weekends
Ability to complete required training within designated timeframe
Attention and Focus
Customer Service and Team Orientation
Communication Skills
Mathematical Reasoning

Job Responsibility

Lead and develop a pharmacy team that provides exceptional patient care
Support novel program awareness, onboard newly hired pharmacy team members, and recognize colleagues for their success
Exhibit best practices when working the bench
Direct and effective management of their pharmacy team
Living our purpose by helping to manage and improve patient health through safe and appropriate dispensing, counseling, and immunizing practices
Overseeing the pharmacy team during bench shifts
Supporting safe and accurate prescription fulfillment
Contributing to positive patient experiences
Proactively offering and delivering immunizations
Supporting the effective management of pharmacy inventory

What we offer

Affordable medical plan options
401(k) plan (including matching company contributions)
Employee stock purchase plan
No-cost programs for all colleagues including wellness screenings, tobacco cessation and weight management programs, confidential counseling and financial coaching
Paid time off
Flexible work schedules
Family leave
Dependent care resources
Colleague assistance programs
Tuition assistance

Fulltime

New

Piling Supervisor

JRL Civil Engineering are looking for a Piling Supervisor for London Projects. T...

Location

United Kingdom , London

Salary:

Not provided

JRL Group

Expiration Date

Until further notice

Requirements

Experience required in the piling industry
Experience of civil construction supervision
Must have CSCS Card & SSSTS Card
First Aid at Work

Job Responsibility

Ensuring site works are carried out in a safe manner in accordance with project specific Method Statements, Risk Assessments and Pile Design. Briefing all operatives involved and ensuring they follow all health & Safety and quality procedures
Co-ordinating daily programmes of work with our Client/Main Contractor to ensure optimum performance
Reporting product and quality non-conformances to Contract Management
Preparing site records
Ensuring project specific Method Statements, Risk Assessments remain current
Carrying out weekly toolbox talks and recording attendees
Ensuring all plant and operators have appropriate certification
Complete weekly safety report and notify Contract Management of any matters requiring review
Raising safety and welfare issues with Client/Main Contractor site management
Informing Contract Management of any incidents or accidents

What we offer

Competitive salary, with confidence of working for an established and growing company
Company Pension Scheme
Private Healthcare
Opportunity for progression within the business
An opportunity to work on some of the nation’s most exciting Construction projects
Dedicated Training & Development Department
A stimulating & dynamic environment
Team bonding events
Sporting Events – perfect for the keen cyclist/runner

Fulltime

New

Aerial Ropeway Design Expert

We are pursuing an opportunity with the Department of Surface Transport, Ministr...

Location

Bhutan

Salary:

Not provided

Agrotec Spa

Expiration Date

March 27, 2026

Requirements

Bachelor’s degree in mechanical, Electrical, or Civil Engineering or relevant field
Minimum 7 years of experience in detailed aerial ropeway design
Experience in alignment, pylon, foundation, and station design
He or she must have served as a designer or technical expert in at least two comparable completed projects of similar complexity
The expert is expected to possess sound knowledge of relevant technical specifications, including pylon design, station design, cable tensioning, and material specifications

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Biostatistician II

iconplc

Location:

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 21, 2026

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Category:Research and Development

Contract Type:Not provided

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Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:March 21, 2026

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