The demand for Statisticians is projected to see steady growth, reflecting the increasing importance of data analysis across various sectors. Statisticians apply statistical theories and methods to solve practical problems in business, engineering, healthcare, and other fields. They collect, analyze, and interpret data to identify trends and relationships, helping organizations make informed decisions. Job opportunities for Statisticians can be found in government agencies, research institutions, pharmaceutical companies, and financial firms.134 Statistician jobs in the United States
Statistician
Posted 1 day ago
Job Viewed
Job Description
Job Category: Science
Time Type: Full time
Minimum Clearance Required to Start: Public Trust
Employee Type: Regular
Percentage of Travel Required: None
Type of Travel: None
* * *
The Opportunity:
We're seeking a highly competent Statistician to join our public health team, with a focus on analyzing surveillance data to identify trends, evaluate interventions, and inform data-driven decision-making. This role requires not only technical expertise but also the ability to clearly communicate findings to both technical and non-technical audiences, translating numbers into actionable insights. The right candidate is more than a number cruncher-they're a strategic thinker and self-starter who takes initiative, drives analytical efforts forward, and thrives in a mission-driven environment.
Responsibilities:
- Apply statistical methods to analyze large-scale public health surveillance datasets.
- Identify and interpret health trends, patterns, and emerging threats
- Evaluate the effectiveness of public health programs and interventions
- Develop models and forecasting tools to support public health planning
- Translate complex statistical findings into clear reports, visualizations, and presentations for diverse stakeholders.
- Collaborate with epidemiologists, data scientists, and public health officials to support data-informed decision-making.
- Ensure quality control and integrity of datasets through rigorous validation and cleaning
- Contribute to the design of new surveillance studies or data collection initiatives - Take ownership of analytical projects and drive efforts independently with minimal oversight - Stay current with advances in statistical methodologies and public health research
Qualifications:
- Master's degree in Biostatistics, Statistics, Public Health, or a related field
- At least 10 years of experience in statistical analysis, ideally in public health or a similar domain
- Demonstrated ability to take initiative and manage complex projects independently
- Excellent written and verbal communication skills, including the ability to present findings clearly to diverse audiences
Desired:
CDC or other public health experience
-
**___**
**What You Can Expect:**
**A culture of integrity.**
At CACI, we place character and innovation at the center of everything we do. As a valued team member, you'll be part of a high-performing group dedicated to our customer's missions and driven by a higher purpose - to ensure the safety of our nation.
**An environment of trust.**
CACI values the unique contributions that every employee brings to our company and our customers - every day. You'll have the autonomy to take the time you need through a unique flexible time off benefit and have access to robust learning resources to make your ambitions a reality.
**A focus on continuous growth.**
Together, we will advance our nation's most critical missions, build on our lengthy track record of business success, and find opportunities to break new ground - in your career and in our legacy.
**Your potential is limitless.** So is ours.
Learn more about CACI here. ( Range** : There are a host of factors that can influence final salary including, but not limited to, geographic location, Federal Government contract labor categories and contract wage rates, relevant prior work experience, specific skills and competencies, education, and certifications. Our employees value the flexibility at CACI that allows them to balance quality work and their personal lives. We offer competitive compensation, benefits and learning and development opportunities. Our broad and competitive mix of benefits options is designed to support and protect employees and their families. At CACI, you will receive comprehensive benefits such as; healthcare, wellness, financial, retirement, family support, continuing education, and time off benefits. Learn more here ( .
The proposed salary range for this position is:
$68,400-$143,700
_CACI is_ _an Equal Opportunity Employer._ _All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, age, national origin, disability, status as a protected veteran, or any_ _other protected characteristic._
Warehouse Statistician
Posted 1 day ago
Job Viewed
Job Description
Job Summary: Key Responsibilities: Operate strictly according to documents, promptly and accurately input various records Handle ERP account management for raw materials and finished products in the warehouse, maintain reports and update them regularly. Monitor and report on stagnant or defective materials for timely follow-up and resolution. Process material work order issuance in the MES system, maintain and update ledgers, and ensure smooth closure of workshop work orders. Ensure accurate and timely printing of module barcodes. Responsible for form inspections, and material preparation operations Assist warehouse site administrators with weekly cycle counts of inventory and support the finance department with monthly stock counts to verify consistency between records and actual stock Archive all original documents for warehouse transactions in chronological order to ensure ease of retrieval Timely and accurate completion of billing, system data entry, and electronic ledger maintenance with 100% accuracy Audit pass rate for all accounts and documents at 100%, with reconciliation completed daily Consistency between material accounts and timely send updated reports within the stipulated time frame Timely closure rate of work orders Other Key Competency Indicators (KCI) Sense of responsibility, teamwork, and time management skills Qualifications: High School Diploma or related experience Proficiency in Excel and other office software Basic understanding of ERP, MES and WMS systems, or significant experience with one of these systems at a high proficiency level Working conditions: Works in manufacturing and warehouse environment Must be comfortable working in a fast-paced, rapidly changing environment May be required to work after hours and on weekends or holidays Physical requirements: Exerting up to 50 pounds occasionally, and/or up to 20 pounds of force constantly to move objects *MON
Compliance Statistician
Posted 1 day ago
Job Viewed
Job Description
Become a Compliance Statistician at Southern California Edison (SCE) and build a better tomorrow. In this job, you'll play a pivotal role in shaping and advancing SCE's compliance analytics strategy. You'll partner across departments to develop meaningful metrics, drive data-informed decisions, and strengthen our compliance posture through collaboration and insight . As a Compliance Statistician, your work will help power our planet, reduce carbon emissions and create cleaner air for everyone. Are you ready to take on the challenge to help us build the future?
**Responsibilities**
+ Leads the development of company standards and efficient processes for statistical activities
+ Provides statistical data analysis matched to purpose. Leverages data visualization, holistic multivariate analysis and nonstandard approaches to deliver additional insights and scientific understanding, where potentially beneficial and exploitable
+ Ensures statistically sound study designs including sample size estimation
+ Reviews and prepares formal written reports/documents for distribution within and outside the department
+ Delivers statistics deliverables for projects to meet schedules and goals for multiple businesses and platforms. Develops/revises work plans independently with consultation with manager
+ Carries out statistical data analysis and statistical computing using sophisticated software tools
+ Conducts research to understand sophisticated problems and to identify new statistical techniques and methods
+ Provides support for continuous improvement activities for various functions through the application of statistical methods to improve product quality, cost, and delivery
+ Interfaces with various database platforms to pull data and link them logically; know how to deal with the inherent structure of the data
+ Analyzes large data sets impacting ethics and/or compliance and extracting relevant insights from them through use of statistical software and programming languages
+ A material job duty of all positions within the Company is ensuring the protection of all its physical, financial and cybersecurity assets, and properly accessing and managing private customer data, proprietary information, confidential medical records, and other types of highly sensitive information and data with the highest standards of conduct and integrity.
**Minimum Qualifications**
+ Bachelor's Degree in Computer Science, Information Systems, Engineering, Statistics/ Mathematics or equivalent STEM major
+ Seven or more years of experience in data mining or statistics modeling.
Preferred Qualifications
+ Experience in an analytical consulting environment
+ Experience using data and statistical models to make strategic business recommendations.
+ Experience with advanced analytics tools and technologies such as R, Python, SAS, or SQL
+ Experience applying machine learning or artificial intelligence (AI) to advanced analytics
+ Experience making presentions to leadership teams and stakeholders
+ Experience working with compliance data
Additional Information
+ This position's work mode is hybrid. The employee will report to an SCE facility for a set number of days with the option to work remotely on the remaining days? Unless otherwise noted, employees are required to work and reside in the state of California? Further details of this work mode will be discussed at the interview stage. The work mode can be changed based on business needs.
+ Visit our Candidate Resource ( page to get meaningful information related to benefits, perks, resources, testing information, hiring process, and more!
+ Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
+ Relocation does not apply to this position.
About Southern California Edison
The people at SCE don't just keep the lights on. Our mission is so much bigger. We're fueling the kind of innovation that's changing an entire industry, and quite possibly the planet. Join us and create a future with cleaner energy, while providing our customers with the safety and reliability they demand. At SCE, you'll have a chance to grow personally and professionally, making a real impact in Southern California and around the world.
Southern California Edison is a proud Equal Opportunity Employer, including disability and protected veteran status.
We are committed to ensuring that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodations at ( .
Mathematical Statistician
Posted 10 days ago
Job Viewed
Job Description
Biostatistician (Digital)
**Travel Required** **:**
None
**Clearance Required** **:**
Ability to Obtain Public Trust
**What You Will Do** **:**
We are currently searching for Mathematical Statistician to support the overall operational objectives of the National Heart, Lung, and Blood Institute (NHLBI) through the provision of support services. This is a full-time, on-site opportunity in Bethesda, MD.
+ Collaborate with investigators on the design, conduct, interpretation, and/or analysis of direct-data projects to answer questions regarding heart, lung, and blood diseases and major risk factors to account for previously unexplained phenomena and/or open significant new avenues for further study.
+ Prepare data and/or results for presentation and/or publication in collaboration with investigator(s).
+ Validate or modify scientific theories or methodologies relating to topic areas to result in improved understanding of techniques or medical practice.
+ Apply conventional, established approaches, methods, techniques, and solutions to new situations or develop new analytical techniques.
+ Develop new hypotheses and approaches for studies using state-of-the-art methods as appropriate.
+ Provide expert statistical consultation to and collaborate with scientists within the NHLBI and associated research groups.
+ Select and implement appropriate methods of study design, data collection, summary, and analysis in the biological and medical sciences.
+ Apply a variety of statistical techniques such as analysis of variance, probability, regression analysis, contingency tables, survival analysis, tests of significance, confidence intervals, and sample size requirements for clinical data.
+ Work with investigators to turn general research objectives into well-defined scientific and testable statistical hypotheses. Determine whether the available data or the data to be collected will allow the hypotheses to be tested.
+ Evaluate methodologies used and ensure results are valid and reliable.
+ Resolve technical problems in collection of biomedical information data.
+ Assist in the development and implementation of quality control and other study-monitoring procedures.
+ Contribute to the initiation of research projects in the application or modifications of mathematical statistics required for data analysis or for statistical investigations.
+ Participate in regularly scheduled branch meetings; discuss data and/or results.
+ Contribute to the writing and editing of scientific papers.
+ Keep abreast of statistical developments through review of literature, attending professional meetings, conferences, and symposia.
+ Other duties as assigned.
**What You Will Need** **:**
+ PhD Degree or master's degree plus three (3) years of experience in lieu of PhD.
+ At least EIGHT (8) years of statistical data analysis related experience.
+ Experience working with statistical software such as R or S+, Python and/or SAS.
+ Significant experience in large-scale data analysis.
+ Must be able to OBTAIN and MAINTAIN a Federal or DoD "PUBLIC TRUST"; candidates must obtain approved adjudication of their PUBLIC TRUST prior to onboarding with Guidehouse. Candidates with an ACTIVE PUBLIC TRUST or SUITABILITY are preferred.
**What Would Be Nice To Have** **:**
+ Knowledge of Microsoft 365
+ Excellent analytical, organizational and time-management skills.
+ Strong communications skills, both oral and written.
The annual salary range for this position is $130,000.00-$216,000.00. Compensation decisions depend on a wide range of factors, including but not limited to skill sets, experience and training, security clearances, licensure and certifications, and other business and organizational needs.
**What We Offer:**
Guidehouse offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects our commitment to creating a diverse and supportive workplace.
Benefits include:
+ Medical, Rx, Dental & Vision Insurance
+ Personal and Family Sick Time & Company Paid Holidays
+ Parental Leave
+ 401(k) Retirement Plan
+ Group Term Life and Travel Assistance
+ Voluntary Life and AD&D Insurance
+ Health Savings Account, Health Care & Dependent Care Flexible Spending Accounts
+ Transit and Parking Commuter Benefits
+ Short-Term & Long-Term Disability
+ Tuition Reimbursement, Personal Development, Certifications & Learning Opportunities
+ Employee Referral Program
+ Corporate Sponsored Events & Community Outreach
+ Care.com annual membership
+ Employee Assistance Program
+ Supplemental Benefits via Corestream (Critical Care, Hospital Indemnity, Accident Insurance, Legal Assistance and ID theft protection, etc.)
+ Position may be eligible for a discretionary variable incentive bonus
**About Guidehouse**
Guidehouse is an Equal Opportunity Employer-Protected Veterans, Individuals with Disabilities or any other basis protected by law, ordinance, or regulation.
Guidehouse will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of applicable law or ordinance including the Fair Chance Ordinance of Los Angeles and San Francisco.
If you have visited our website for information about employment opportunities, or to apply for a position, and you require an accommodation, please contact Guidehouse Recruiting at 1- or via email at . All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodation.
All communication regarding recruitment for a Guidehouse position will be sent from Guidehouse email domains including @guidehouse.com or . Correspondence received by an applicant from any other domain should be considered unauthorized and will not be honored by Guidehouse. Note that Guidehouse will never charge a fee or require a money transfer at any stage of the recruitment process and does not collect fees from educational institutions for participation in a recruitment event. Never provide your banking information to a third party purporting to need that information to proceed in the hiring process.
If any person or organization demands money related to a job opportunity with Guidehouse, please report the matter to Guidehouse's Ethics Hotline. If you want to check the validity of correspondence you have received, please contact . Guidehouse is not responsible for losses incurred (monetary or otherwise) from an applicant's dealings with unauthorized third parties.
_Guidehouse does not accept unsolicited resumes through or from search firms or staffing agencies. All unsolicited resumes will be considered the property of Guidehouse and Guidehouse will not be obligated to pay a placement fee._
Safety Expert Statistician
Posted today
Job Viewed
Job Description
About the Job:
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate Progress. Join our Biostatistics team as a Safety Expert Statistician and you'll be supporting our V division with your safety data analysis talents to support safety monitoring teams.
Job Summary
Provide leadership and guidance as the lead statistician dedicated to safety on one or more safety monitoring team(s), accountable for all methodological and statistical aspects for safety data analyses around pooled clinical trial data of project(s). Act as statistical consultant within company for safety analyses, also on individual trial level.
Major Duties and Responsibilities
Lead safety signal detection, validation, charaterisation and reporting for several projects with minimal direction from group head, direct statistical support and provide statistical scientific leadership for clinical trial safety data within a project. Accountable for statistical aspects for safety analysis, including quality, relevance to external stakeholders (e.g. regulatory authorities, medical journals), and scientific validity.
Accountable for all safety statistical deliverables for complex projects
Promote teamwork, quality, operational efficiency, and innovation. Ensure safety monitoring team compliance with SOPs and departmental standards.
Plan and track project activities related to safety, timelines, and resource use. Provide justification for planned resource needs. Seek to optimize resource utilization thru efficient and well-managed resource allocation and across projects or areas. . Capacity to respond to unscheduled increase in workload.
Lead discussion around definition and harmonization of quality standards also on individual trial level within and across therapeutic areas.
Provide technical guidance and mentoring to junior staff.
Ensure productive collaborations with other functions in the safety monitoring team and with other statistics project leaders and in communicating with senior leadership.
Represent statistics to participate (and lead if applicable) in scientific or technology working groups or cross function initiatives. Contribute to operation process optimization. Develop, promote state-of-the-art methodology and standards for safety analyses.
About you:
PhD/MS in statistics or related discipline with 6 years of pharmaceutical experience Knowledge of epidemiology methods and concepts in safety context
Demonstrated strong project/study management, interpersonal and communication skills
Broad knowledge and good understanding of advanced statistical concepts and techniques, including bayesian methodology
Broad experience in clinical development or post-marketing activities such a submissions, interactions with regulatory agencies or other external stakeholders
Experience safety signal detection desired
Ability to represent Sanofi in cross-company activities such a consortiums or professional associations
Ability and mindset to embrace change, innovate and continuously improve practice
Why Choose Us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SA
#LI-SA
#LI-Hybrid
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.
Safety Expert Statistician
Posted today
Job Viewed
Job Description
About the Job:
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate Progress. Join our Biostatistics team as a Safety Expert Statistician and you'll be supporting our V division with your safety data analysis talents to support safety monitoring teams.
Job Summary
Provide leadership and guidance as the lead statistician dedicated to safety on one or more safety monitoring team(s), accountable for all methodological and statistical aspects for safety data analyses around pooled clinical trial data of project(s). Act as statistical consultant within company for safety analyses, also on individual trial level.
Major Duties and Responsibilities
Lead safety signal detection, validation, charaterisation and reporting for several projects with minimal direction from group head, direct statistical support and provide statistical scientific leadership for clinical trial safety data within a project. Accountable for statistical aspects for safety analysis, including quality, relevance to external stakeholders (e.g. regulatory authorities, medical journals), and scientific validity.
Accountable for all safety statistical deliverables for complex projects
Promote teamwork, quality, operational efficiency, and innovation. Ensure safety monitoring team compliance with SOPs and departmental standards.
Plan and track project activities related to safety, timelines, and resource use. Provide justification for planned resource needs. Seek to optimize resource utilization thru efficient and well-managed resource allocation and across projects or areas. . Capacity to respond to unscheduled increase in workload.
Lead discussion around definition and harmonization of quality standards also on individual trial level within and across therapeutic areas.
Provide technical guidance and mentoring to junior staff.
Ensure productive collaborations with other functions in the safety monitoring team and with other statistics project leaders and in communicating with senior leadership.
Represent statistics to participate (and lead if applicable) in scientific or technology working groups or cross function initiatives. Contribute to operation process optimization. Develop, promote state-of-the-art methodology and standards for safety analyses.
About you:
PhD/MS in statistics or related discipline with 6 years of pharmaceutical experience Knowledge of epidemiology methods and concepts in safety context
Demonstrated strong project/study management, interpersonal and communication skills
Broad knowledge and good understanding of advanced statistical concepts and techniques, including bayesian methodology
Broad experience in clinical development or post-marketing activities such a submissions, interactions with regulatory agencies or other external stakeholders
Experience safety signal detection desired
Ability to represent Sanofi in cross-company activities such a consortiums or professional associations
Ability and mindset to embrace change, innovate and continuously improve practice
Why Choose Us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SA
#LI-SA
#LI-Hybrid
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.
Principal Computational Statistician
Posted 1 day ago
Job Viewed
Job Description
**Organization Overview:**
At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.
**Responsibilities**
**Statistical Analysis:**
+ Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans, write reports and communicate results, assist/respond to regulatory queries.
+ Assist in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the analysis plan, and conducting the actual analysis once a reporting database is created.
+ Collaborate with data management in the planning and implementation of data quality assurance plans.
+ Maintain proficiency with respect to SAS/R programming and statistical methodology and in applying new and varied methods.
+ Effectively justify methods selected and implement previously outlined analysis plans.
+ Conduct peer-review of work products from statistical colleagues.
+ Effectively use current technologies and available tools for conducting the clinical trial analysis.
+ Responsible for assisting in the communication of study results via regulatory submissions, and manuscripts, as well as for communicating one-on-one with key customers.
**Therapeutic Area and Systems Knowledge:**
+ Understand relevant disease states in order to enhance the level of customer focus and collaboration.
+ Ensure replication of tools and systems, where applicable and stay informed of technological advances.
**Regulatory and Quality Compliance:**
+ Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable corporate, medical, local, and departmental policies, procedures, processes, and training.
**Basic Qualifications**
+ Master's degree in Statistics, Biostatistics or MSPH with concentration in Statistics or Biostatistics, or relevant areas of science
+ 3+ years of statistical analysis/programming experience
**Additional Skills/Preferences**
+ Proficiency in statistical programming languages/software such as SAS, R, Spotfire, etc.
+ Interpersonal/teamwork skills for effective interactions
+ Technical growth and application with solid understanding of statistics and statistical software
+ Self-management skills with a focus on results for prompt and accurate completion of competing deliverables
+ Creativity and innovation
+ Demonstrated problem solving ability and attention to detail.
+ Data analysis, technology, and systems expertise
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$105,000 - $182,600
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly
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Principal Computational Statistician
Posted 4 days ago
Job Viewed
Job Description
**Responsibilities**
**Statistical Analysis:**
+ Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans, write reports and communicate results, assist/respond to regulatory queries.
+ Assist in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the analysis plan, and conducting the actual analysis once a reporting database is created.
+ Collaborate with data management in the planning and implementation of data quality assurance plans.
+ Maintain proficiency with respect to SAS/R programming and statistical methodology and in applying new and varied methods.
+ Effectively justify methods selected and implement previously outlined analysis plans.
+ Conduct peer-review of work products from statistical colleagues.
+ Effectively use current technologies and available tools for conducting the clinical trial analysis.
+ Responsible for assisting in the communication of study results via regulatory submissions, and manuscripts, as well as for communicating one-on-one with key customers.
**Therapeutic Area and Systems Knowledge:**
+ Understand relevant disease states in order to enhance the level of customer focus and collaboration.
+ Ensure replication of tools and systems, where applicable and stay informed of technological advances.
**Regulatory and Quality Compliance:**
+ Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable corporate, medical, local, and departmental policies, procedures, processes, and training.
**Basic Qualifications**
+ Master's degree in Statistics, Biostatistics or MSPH with concentration in Statistics or Biostatistics, or relevant areas of science
+ 3+ years of statistical analysis/programming experience
**Additional Skills/Preferences**
+ Proficiency in statistical programming languages/software such as SAS, R, Spotfire, etc.
+ Interpersonal/teamwork skills for effective interactions
+ Technical growth and application with solid understanding of statistics and statistical software
+ Self-management skills with a focus on results for prompt and accurate completion of competing deliverables
+ Creativity and innovation
+ Demonstrated problem solving ability and attention to detail.
+ Data analysis, technology, and systems expertise
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$93,750 - $200,200
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly
Safety Expert Statistician
Posted 15 days ago
Job Viewed
Job Description
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress. Join our Biostatistics team as a Safety Expert Statistician and you'll be supporting our V division with your safety data analysis talents to support safety monitoring teams.
**Job Summary**
Provide leadership and guidance as the lead statistician dedicated to safety on one or more safety monitoring team(s), accountable for all methodological and statistical aspects for safety data analyses around pooled clinical trial data of project(s). Act as statistical consultant within company for safety analyses, also on individual trial level.
**Major Duties and Responsibilities**
+ Lead safety signal detection, validation, charaterisation and reporting for several projects with minimal direction from group head, direct statistical support and provide statistical scientific leadership for clinical trial safety data within a project. Accountable for statistical aspects for safety analysis, including quality, relevance to external stakeholders (e.g. regulatory authorities, medical journals), and scientific validity.
+ Accountable for all safety statistical deliverables for complex projects
+ Promote teamwork, quality, operational efficiency, and innovation. Ensure safety monitoring team compliance with SOPs and departmental standards.
+ Plan and track project activities related to safety, timelines, and resource use. Provide justification for planned resource needs. Seek to optimize resource utilization thru efficient and well-managed resource allocation and across projects or areas. . Capacity to respond to unscheduled increase in workload.
+ Lead discussion around definition and harmonization of quality standards also on individual trial level within and across therapeutic areas.
+ Provide technical guidance and mentoring to junior staff.
+ Ensure productive collaborations with other functions in the safety monitoring team and with other statistics project leaders and in communicating with senior leadership.
+ Represent statistics to participate (and lead if applicable) in scientific or technology working groups or cross function initiatives. Contribute to operation process optimization. Develop, promote state-of-the-art methodology and standards for safety analyses.
**About you:**
+ PhD/MS in statistics or related discipline with 6 years of pharmaceutical experience Knowledge of epidemiology methods and concepts in safety context
+ Demonstrated strong project/study management, interpersonal and communication skills
+ Broad knowledge and good understanding of advanced statistical concepts and techniques, including bayesian methodology
+ Broad experience in clinical development or post-marketing activities such a submissions, interactions with regulatory agencies or other external stakeholders
+ Experience safety signal detection desired
+ Ability to represent Sanofi in cross-company activities such a consortiums or professional associations
+ Ability and mindset to embrace change, innovate and continuously improve practice?
**Why Choose Us?**
+ Bring the miracles of science to life alongside a supportive, future-focused team.
+ Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
+ Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
+ Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SA ?
#LI-SA?
#LI-Hybrid
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
_US and Puerto Rico Residents Only_
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
_North America Applicants Only_
The salary range for this position is:
$147,000.00 - $212,333.33
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK ( .
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (
Safety Expert Statistician
Posted 15 days ago
Job Viewed
Job Description
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress. Join our Biostatistics team as a Safety Expert Statistician and you'll be supporting our V division with your safety data analysis talents to support safety monitoring teams.
**Job Summary**
Provide leadership and guidance as the lead statistician dedicated to safety on one or more safety monitoring team(s), accountable for all methodological and statistical aspects for safety data analyses around pooled clinical trial data of project(s). Act as statistical consultant within company for safety analyses, also on individual trial level.
**Major Duties and Responsibilities**
+ Lead safety signal detection, validation, charaterisation and reporting for several projects with minimal direction from group head, direct statistical support and provide statistical scientific leadership for clinical trial safety data within a project. Accountable for statistical aspects for safety analysis, including quality, relevance to external stakeholders (e.g. regulatory authorities, medical journals), and scientific validity.
+ Accountable for all safety statistical deliverables for complex projects
+ Promote teamwork, quality, operational efficiency, and innovation. Ensure safety monitoring team compliance with SOPs and departmental standards.
+ Plan and track project activities related to safety, timelines, and resource use. Provide justification for planned resource needs. Seek to optimize resource utilization thru efficient and well-managed resource allocation and across projects or areas. . Capacity to respond to unscheduled increase in workload.
+ Lead discussion around definition and harmonization of quality standards also on individual trial level within and across therapeutic areas.
+ Provide technical guidance and mentoring to junior staff.
+ Ensure productive collaborations with other functions in the safety monitoring team and with other statistics project leaders and in communicating with senior leadership.
+ Represent statistics to participate (and lead if applicable) in scientific or technology working groups or cross function initiatives. Contribute to operation process optimization. Develop, promote state-of-the-art methodology and standards for safety analyses.
**About you:**
+ PhD/MS in statistics or related discipline with 6 years of pharmaceutical experience Knowledge of epidemiology methods and concepts in safety context
+ Demonstrated strong project/study management, interpersonal and communication skills
+ Broad knowledge and good understanding of advanced statistical concepts and techniques, including bayesian methodology
+ Broad experience in clinical development or post-marketing activities such a submissions, interactions with regulatory agencies or other external stakeholders
+ Experience safety signal detection desired
+ Ability to represent Sanofi in cross-company activities such a consortiums or professional associations
+ Ability and mindset to embrace change, innovate and continuously improve practice?
**Why Choose Us?**
+ Bring the miracles of science to life alongside a supportive, future-focused team.
+ Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
+ Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
+ Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SA ?
#LI-SA?
#LI-Hybrid
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
_US and Puerto Rico Residents Only_
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
_North America Applicants Only_
The salary range for this position is:
$147,000.00 - $212,333.33
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK ( .
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (