Biostatistician Job at Chickasaw Nation Industries, Inc (CNI)

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 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

Clinical Data Manager

Companies in the veterinary and animal feed sectors require qualified support fo...

Location

Germany , Munich

Salary:

Not provided

Argenta

Expiration Date

Until further notice

Requirements

Proficiency in using IT systems
Basic database knowledge, ideally additional programming and coding skills
Basic understanding of natural sciences
Excellent written and spoken German and English skills
Ability to work independently in project teams
Reliable work ethic and strong communication and coordination skills
Flexibility and teamwork skills
Willingness to learn new tasks and areas of expertise
Ideally, you will have completed vocational training with a qualification in clinical data management or hold a degree in a natural science

Job Responsibility

Planning study-specific setups for data collection in various EDC and database systems
Database design and creation of data capture forms, design and implementation of plausibility checks
Supporting quality assurance during the validation and acceptance of these systems
Managing the electronic collection of study data
Handling query processes
Data quality assurance
Coordinating external data providers, data transfer setup: importing and exporting
Data transfer to the biostatistician

What we offer

Detailed introduction to your field of work
Challenging field of activity contributing to the availability of animal health products
Working in an international team with modern equipment
Family-friendly environment
Options for continuous education
Very positive and collegial team atmosphere in Munich

New

Clinical Data Validation Engineer Specialist

We are currently seeking a Senior Clinical Data Science Programmer to join our d...

Location

India , Bangalore

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

Director, Statistical Innovation

Join Amgen’s Mission of Serving Patients. At Amgen, if you feel like you’re part...

Location

United States

Salary:

226377.00 - 258078.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 4 years of Biostatistics/Statistical experience
Master’s degree and 8 years of Biostatistics/Statistical experience
Bachelor’s degree and 10 years of Biostatistics/Statistical experience
10 years of post-graduate statistical experience in the biopharmaceutical industry in clinical trial design, implementation, analysis and reporting
Statistical expertise and leadership across drug development phases, regulatory submissions, and payer interactions
Excellent computing, modelling and simulation skills using R, SAS, WinBugs, FACTS, etc.
Doctorate in Statistics/Biostatistics and post-graduate statistical experience in the pharmaceutical industry or medical research
Proven experience with both conventional and innovative trial designs (including adaptive and/or Bayesian) in different phases of drug development
Expertise in advanced statistical analysis methods, modeling and simulation
Knowledge of multiple disease areas and related regulatory guidelines

Job Responsibility

Guides Product Strategy and Study Design
Promotes innovative design options and fit-for-purpose analysis approaches that address appropriate clinical questions in protocol / program design and balance speed, quality, and cost
Provides advisory input in the development of the Global Statistical Strategic Plan (GSSP) to align study design and statistical approaches with product strategy and Evidence Generation Plan (EGP)
Reviews key phase 2 and 3 protocols and provides input during the TA TRC review
Provides Technical Expertise
Provides technical expertise to GSL and EGT on innovative study designs and advanced analytical methods
Provides design options and simulation specifications to the Simulation and Modeling team and develops and approves the simulation plan and results
Interprets and communicates modeling and simulation results to inform and guide the selection of optimal trial designs
Provides guidance and training to the Simulation and Modeling biostatisticians
Builds Cross-functional Network

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models, including remote and hybrid work arrangements, where possible

Fulltime