For over 40 years, our team of 1,000+ experienced professionals have provided the full range of Contract Research Organization expertise necessary to conduct clinical research with a firm scientific basis that is fully compliant with national and international regulatory guidelines.  With offices throughout the US, Europe, Canada, and India, Emmes supports the advancement of global public health and biopharmaceutical innovation through disciplined science, rigorous research, fact-based decision-making, and operational excellence. 

Emmes possesses knowledge across a broad range of therapeutic areas, with specializations in Vaccines and Infectious Diseases, Ophthalmology, Immunology and Neuroscience.  From comprehensive support of pandemic research to groundbreaking work in cell and gene therapy across the globe, Emmes has collaborated on clinical research across a wide array of disease states in over 75 nations.  

As a strategic collaborator with applied talent in over 2,000 clinical trials and contributions to over 2,500 publications that advance the understanding of medicine and public health, Emmes is committed to expanding the services offered to best meet the changing needs of clients and studies.  Ongoing investments in global clinical research capabilities, innovative data management platforms, biostatistics/bioinformatics expertise, and people have enabled Emmes to provide a multi-faceted approach to help you meet your research objectives.

Emmes is a diverse, inclusive, innovative CRO that values integrity, agility, passion for excellence, collaborative partnerships, and intellectual curiosity.

Industry: Research Services
Company Size: 1,001-5,000 employees

Emmes

Savvy Admin PROD

**Senior Biostatistician **

**US Remote **

Emmes Group: Building a better future for us all.

Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.

We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!

**Primary Purpose **

Leads collaborations with clinical investigators to determine study design, contributes to protocol development, authors statistical analysis plans, performs statistical analysis, makes statistical inference and writes and presents reports summarizing findings including publications in peer reviewed journals. Manages statistical activities for a clinical study or platform of clinical studies.

- Provides sound strategic, scientific and statistical input to support client's research projects.

- Serves as the lead Biostatistician on one or more study projects.

- May supervise Biostatisticians, Associate Biostatisticians and SAS programmers (all levels) and direct their work on clinical research studies.

- Leads the project team's development of study analysis plans and statistical programs to perform analyses and display study data.

- Keeps abreast with current statistical and medical literature to ensure that sound methodologies are adopted.

- Fosters innovation in Biostatistics that will continuously enhance current statistical knowledge and practices.

- Ensures the scientific integrity of the research project and the accuracy of the reported results.

- Performs sample size calculation and provides leadership in the statistical design of research projects.

- Reviews protocols and case report forms to ensure that protocol objectives are met, and standards are maintained.

- Develops study assignment allocation schemas along with appropriate documentation.

- Leads the development of the methods and results sections of clinical study reports and scientific publications.

- Represents EMMES on behalf of clients at regulatory meetings.

- Participate in the development and updating of Standard Operating Procedures.

- Performs other duties as assigned

- Complies with all policies and standards

- PhD Biostatistics, statistics, epidemiology or related field required

- 4-6 years of related experience is expected but not required for the position.

- 1-3 years Demonstrated proficiency with statistical methods and applications in clinical research required.

- 1-3 years Strong programming skills in SAS and/or R required.

~~Why work at Emmes? ~~

At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our  **Emmes Cares ** community engagement program.   We offer a competitive benefits package focused on the health and needs of our growing workforce, including:

- **Flexible Approved Time Off **

- **Tuition Reimbursement **

- **401k Retirement Plan **

- **Work From Home Anywhere in the US **

- **Maternal/Paternal Leave **

- **Casual Dress Code & Work Environment **

**CONNECT WITH US! **

~~Follow us on Twitter - @EmmesCRO ~~

~~Find us on LinkedIn - Emmes ~~

~~The Emmes Company, LLC is an equal opportunity employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to disability or protected veteran status. ~~

Senior Biostatistician

Guided by the needs of our patients and their families, 
Massachusetts General Hospital aims to deliver the very best health care in a safe, compassionate environment; to advance that care through innovative research and education; and, to improve the health and well-being of the diverse communities we serve.

Visit our careers page!  http://www.mghcareers.org

Industry: Hospitals and Health Care
Company Size: 10,001+ employees

Massachusetts General Hospital

Site: The General Hospital Corporation

Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.

**Job Summary**

The Udler Laboratory in the Center for Genomic Medicine (CGM) at Massachusetts General Hospital (MGH) is seeking a motivated, enthusiastic candidate to join our research group.

Our research group is an interdisciplinary team of clinicians, biostatisticians, and computational biologists who are working together to investigate the use of genetics to improve care of people with diabetes. Our lab spans the CGM and the Diabetes Unit at MGH, as well as the Diabetes Initiative at the Broad Institute. We investigate both common and rare genetic variation contributing to diabetes and utilizes unprecedented sets of genetic data linked to clinical data in massive biobanks and study cohorts. Dr. Udler is the founding director of the MGH Diabetes Genetics Clinic and a member of the ClinGen Monogenic Diabetes Expert Panel. Our lab leads national consortia on the study of rare and atypical diabetes, as well as the heterogeneity of diabetes.

The successful applicant would contribute to both clinical and research capacities. The clinical work would involve working with Dr. Udler to order genetic testing and provide counseling to patients seen in the MGH Diabetes Clinic. The research tasks are clinically motivated and involve performing variant curation for variants in monogenic diabetes genes and assisting with development of novel genetic testing reports that communicate both monogenic and polygenic disease risk. The research tasks are funded in part by an NIH grant aimed at studying variants of intermediate penetrance and involves collaboration with leaders in the field of diabetes genetics and clinical genetics, including Dr. Josep Mercader at MGH/Broad; Dr. Matthew Lebo, Director of the Mass General Brigham Laboratory of Molecular Medicine; and Dr. Toni Pollin, Professor of Genetics at University of Maryland and leader of ClinGen curation efforts in monogenic diabetes.

**Qualifications**

Education

Master's Degree Genetic Counseling required

**Experience**

genetics experience 1-2 years preferred

**Knowledge, Skills And Abilities**

-  Strong patient/customer service skills.

-  Good documentation and organizational skills and good attention to detail.

-  Ability to adhere to detailed survey research protocols.

-  Ability to communicate effectively, both orally and in writing.

-  Strong understanding of molecular genetics and general chemistry.

-  Good attention to detail and analytical.

**Additional Job Details (if Applicable)**

**Remote Type**

Hybrid

**Work Location**

185 Cambridge Street

**Scheduled Weekly Hours**

40

**Employee Type**

Regular

**Work Shift**

Day (United States of America)

**Pay Range**

$66,518.40 - $99,517.60/Annual

**Grade**

5

At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package.

**EEO Statement**

1200 The General Hospital Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a 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. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran’s Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at (857)-282-7642.

**Mass General Brigham Competency Framework**

At Mass General Brigham, our competency framework defines what effective leadership “looks like” by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.

Genetic Counselor

The University of Southern California is a leading private research university located in Los Angeles, the capital of the Pacific Rim.

This is the official LinkedIn presence for the University of Southern California. This account is managed and mediated by the staff of USC University Communications. Content (including posts from 3rd parties) that include videos, photographs, opinions and links to content outside of this channel do not necessarily represent the University of Southern California’s academic goals or opinions. 

Community guidelines: Alumni and students are welcome to post professional updates and news. Posts containing solicitations, product placements, derogatory or inflammatory comments are prohibited and will be removed. Off-topic comments will also be removed. 

Posts are not regularly monitored. Please note: for questions regarding degrees offered and admissions policies please call (213) 740-2311.

Industry: Higher Education
Company Size: 10,001+ employees

University of Southern California

The USC Norris Comprehensive Cancer Center at the University of Southern California (USC Norris) was founded in 1971 and has been continuously funded as an NCI-designated Comprehensive Cancer Center since 1973. USC Norris has a rich tradition of collaborative research and serves as a major regional and national resource for cancer research, prevention, treatment and education.

The Biostatistics Core at the USC Norris has an opening for a biostatistician to support clinical and laboratory research efforts at the Cancer Center. We are seeking a Biostatistician I to support a wide range of cancer research projects spanning basic, translational, and population sciences. Candidates should have solid training in biostatistics, statistics, data science, or a related quantitative field. Experience with clinical trial data analysis is preferred; exposure to bioinformatics or high-dimensional data is a plus. The ideal candidate is a fast and enthusiastic learner who can adapt to rapidly evolving data types and analytical methods. This role requires strong teamwork, a service-oriented mindset, and excellent communication skills (written and verbal). A positive attitude and strong work ethic are essential in our collaborative core environment.

The biostatistician will work together with faculty statistician to provide statistical support to Cancer Center researchers. This individual will contribute to the design and planning of research studies and experiments. This will involve evaluating, recommending, and implementing procedures for data acquisition, management, and quality control; evaluating and recommending statistical methods for data analysis; monitoring study progress and interpreting the results of analysis; and preparing technical reports and papers on study plans, progress, and results of research activities. In addition, this biostatistician should have strong expertise in the high dimensional data analysis area.

**Essential Job Duties Include, But Are Not Limited To**

- Assist Core faculty in grant and protocol development, including sample size and power calculations, endpoint definition, and specification of planned statistical methods.

- Support clinical trial work by contributing to protocol development, statistical analysis plans, interim and final analyses, and preparation of tables/figures for trial reports and publications.

- Perform data management and statistical analysis (e.g., in R, SAS, or Python), including data cleaning, creation of analysis datasets, and quality checks for a variety of cancer-related data types.

- Conduct descriptive and inferential analyses, fit appropriate statistical models, and help interpret results in a clinically and biologically meaningful way.

- Prepare clear tables, figures, and concise summaries of methods and results for abstracts, manuscripts, presentations, and internal reports.

- Provide ongoing statistical consultation and support to a wide range of investigators, contributing to effective communication, good research practices, and a collaborative core environment.

**Required Qualifications**

- Candidates should have solid training in biostatistics, statistics, data science, or a related quantitative field

**Preferred Qualifications**

- A positive attitude and strong work ethic are essential in our collaborative core environment.

- Experience in a complex medical or academic development setting encouraged.

- Excellent communication skills – both written and verbal.

- Comfortable interfacing with highest level of university leadership and university supporters/volunteers.

- Demonstrated affinity for diplomacy and the ability to cultivate and maintain relationships at all levels.

- Practices a high level of integrity and honesty in maintaining confidentiality.

- Ability to multi-task effectively and demonstrate strong organizational skills.

- Sound judgment and decision making

- A cooperative and team-oriented attitude

- Effective facilitator in various settings

Follows established USC and department policies, procedures, objectives, performance improvement, attendance, safety, environmental, and infection control guidelines, including adherence to the workplace Code of Conduct and Compliance Plan.

This position is hybrid and employee must report to work at the USC Health Science Campus in Los Angeles, CA when scheduled. Work hours and on-site days may be subject to change depending on business needs.

The annual base salary range for this position is $85,894 - $90,000. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate’s work experience, education/training, key skills, internal peer equity, federal, state and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations.

Minimum Education: Master's degree, Combined experience/education as substitute for minimum education Minimum Experience: 1 year, Combined education/experience as substitute for minimum experience Minimum Field of Expertise: Experience in Biostatistics , Statistics or related field . Experience with SAS, R or STATA.

**Job ID ** REQ20174372 **Posted Date ** 05/04/2026

Apply

Current employees apply here

Biostatistician I

The Emmes Group is where human intelligence meets artificial intelligence. Our mission is dedicated to advancing public health and biopharmaceutical innovation throughout the world. Our CRO business Emmes, founded in 1977, provides clinical services tailored to meet the needs of its public and private sector partners. Our Veridix AI business is focused on delivering innovative technology solutions to create the clinical trial infrastructure of the 21st century. To learn more about how we are modernizing clinical research and having a positive impact on patients' lives, visit www.theemmesgroup.com.

Industry: Research Services
Company Size: 1,001-5,000 employees

Emmes Group

**Overview**

**Biostatistician**

**US Remote**

Emmes Group: Building a better future for us all.

Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.

We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!

**Primary Purpose**

Collaborates with clinical investigators to determine study design, contributes to protocol development, writes statistical analysis plans, performs statistical analysis, makes statistical inference and writes and presents reports summarizing findings including publications in peer-reviewed journals.

**Responsibilities**

- Collaborating with clinical investigators to determine study design;

- Writing sections of protocols that require statistical input;

- Reviewing protocols and case report forms to ensure that protocol objectives are met and standards are maintained;

- Generating treatment allocations in randomized clinical research studies and ensuring proper implementation;

- Leading the project team’s development of statistical analysis plans and programs to perform analyses and display study data;

- Performing statistical analyses; writing and validating application programs;

- Implementing data and safety monitoring reports to ensure participants’ safety;

- Developing metrics and generating quality control reports to optimize the performance of clinical sites and the coordinating center;

- Generating study reports to be distributed to internal and external monitoring committees and regulatory bodies;

- Participating in professional development activities both within and outside the company

- Other duties as assigned

**Qualifications**

- PhD in biostatistics, statistics, epidemiology or related field.

- Demonstrated proficiency with statistical methods and applications in clinical research.

- Strong programming skills in SAS and/or R.

- Ability to manage multiple tasks.

- Ability to work independently, as well as in a team environment.

- Ability to effectively communicate technical concepts, both written and oral.

~~Why work at Emmes?~~

At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our **Emmes Cares ** community engagement program. We offer a competitive benefits package focused on the health and needs of our growing workforce, including:

- Flexible Approved Time Off

- Tuition Reimbursement

- 401k Retirement Plan

- Work From Home Anywhere in the US

- Maternal/Paternal Leave

- Casual Dress Code & Work Environment

**CONNECT WITH US!**

~~Follow us on Twitter - @EmmesCRO~~

~~Find us on LinkedIn - Emmes~~

~~The Emmes Company, LLC is an equal opportunity affirmative action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to disability, protected veteran status, or other legally protected characteristics.~~

Biostatistician

The Alaska Native Tribal Health Consortium is a non-profit Tribal health organization designed to meet the unique health needs of Alaska Native and American Indian people living in Alaska. ANTHC provides world-class health services, which include comprehensive medical services at the Alaska Native Medical Center, wellness programs, disease research and prevention, rural provider training and rural water and sanitation systems construction.

ANTHC is the largest, most comprehensive Tribal health organization in the United States, and Alaska’s second-largest health employer with more than 3,000 employees offering an array of health services to people around the nation’s largest state.

Industry: Hospitals and Health Care
Company Size: 1,001-5,000 employees

Alaska Native Tribal Health Consortium (ANTHC)

ABOUT ANTHC: The Alaska Native Tribal Health Consortium is a non-profit Tribal health organization designed to meet the unique health needs of Alaska Native and American Indian people living in Alaska. In partnership with the more than 171,000 Alaska Native and American Indian people that we serve and the Tribal health organizations of the Alaska Tribal Health System, ANTHC provides world-class health services, which include comprehensive medical services at the Alaska Native Medical Center, wellness programs, disease research and prevention, rural provider training and rural water and sanitation systems construction.

ANTHC is the largest, most comprehensive Tribal health organization in the United States, and Alaska’s second-largest health employer with more than 3,100 employees offering an array of health services to people around the nation’s largest state.

Our vision: Alaska Native people are the healthiest people in the world.

ANTHC’s AMAZING BENEFITS: ANTHC offers a competitive and comprehensive Benefits Package for all Benefit Eligible Employees, which includes:

Medical Insurance provided through the Federal Employee Health Benefits Program as a Tribal Employee, with over 20 plans and tiers.

Cost-Share Dental and Vision Insurances

Discounted Pet Insurance

Retirement Contributions with Pre-Tax or Roth options into a 403(b).

401(a) ANTHC Retirement Plan: After one year of employment, ANTHC will begin making matching contributions of up to 5% of your eligible pay, based on your own contributions. In addition, you may be eligible for an annual discretionary contribution of up to 3% from the employer.

Paid Time Off starts immediately, earning up to 6 hours per pay period, with paid time off accruals increasing based on years of service.

Eleven Paid Holidays

Paid Parental Leave or miscarriage/stillbirth eligibility after six months of employment

Basic Short/Long Term Disability premiums, Accidental Death and Dismemberment (AD&D) Insurance, and Basic Life Insurance are covered 100% by ANTHC, with additional options for Short-Term Disability Buy-Up Coverage and Voluntary Life for yourself and your family members.

Flexible Spending Accounts for Healthcare and Dependent Care.

Ancillary Cash Benefits for accident, hospital indemnity, and critical illness.

On-Site Child Care Facility with expert-designed classrooms for early child development and preschool.

Employee Assistance Program with support for grief, financial counseling, mental/emotional health, and discounted legal advice.

Tuition Discounts for you and your eligible dependents at Alaska Pacific University.

On-Site Training Courses and Professional Development Opportunities.

License and certification reimbursements and occupational insurance for medical staff.

Gym Access to Alaska Pacific University includes a saltwater pool, rock climbing, workout gym, and steep discounts for outdoor equipment rentals.

Emergency Travel Assistance

Education Assistance or Education leave eligibility

Discount program for travel, gym memberships, amusement parks, and more.

Alaska Native Tribal Health Consortium has a hiring preference for qualified Alaska Native and American Indian applicants pursuant to P.L. 93-638 Indian Self Determination Act.

**Position Summary**

Under general direction, the Biostatistician is responsible for analyzing data from public health surveillance, research or quality improvement activities. Assists in preparation of manuscripts and presents findings at national and international conferences. Provides leadership and guidance in biostatistics through consultation on the analysis and interpretation of studies.

**Position Responsibilities**

Associate Biostatistician

Assist in the design and implementation of research, quality improvement and public health surveillance projects.

Assist in developing data collection protocols, data management, and ensuring data quality.

Clean, validate, and organize data for analysis.

Assist in the interpretation of statistical results and preparation of reports and presentations.

Maintain documentation of statistical methods and programming codes.

Performs other duties as assigned.

Biostatistician

**Biostatistician I Duties In Addition To**

Conduct statistical analyses using appropriate methods and software packages.

Analyze and interpret complex datasets using advanced statistical methods.

Prepare statistical analysis plans and conduct statistical analyses using appropriate software.

Generate clear and concise reports and delivers presentations to communicate findings to stakeholders.

Provides statistical education and training and acts as a resource for ANTHC and ANMC staff for statistics-related needs such as data collection, data management and statistical analysis.

Senior Biostatistician

**Biostatistician I And II Duties In Addition To**

Oversee multiple projects, ensuring adherence to timelines, quality standards, and regulatory requirements.

Provide advice to researchers or students regarding study design, sample size determination, power analysis, data management, analysis of data, and presentation of statistical information.

Provide statistical support in grant applications and manuscript preparation.

Contribute to the statistical aspects of the preparation of research proposals, assist in the selection of assessment instruments and contribute to the construction of questionnaires.

Contribute to academic papers, conference papers and/or posters, in particular to the statistical aspects of the above-mentioned.

Develop and validate statistical models for predictive and prognostic analyses.

Participates in relevant research meetings and serves as a member of relevant committees.

Serve as a subject matter expert at scientific conferences and meetings.

Mentors junior biostatisticians.

**KNOWLEDGE And SKILLS**

All

Knowledge of Alaska Tribal Health System, ANTHC, and Alaska Native culture(s).

Knowledge of applicable federal, state, tribal and local regulations and programs.

Knowledge of scientific approach and methodologies.

Knowledge of basic statistical principles.

Basic skill in operating a personal computer utilizing a variety of applications.

Basic skill in statistical programming languages (e.g., R, SAS, Python).

Basic skill in database design and management.

Ability to establish and maintain cooperative working relationships with others.

Ability to manage multiple priorities and tasks concurrently and meet deadlines.

Ability to communicate effectively.

Ability to work in a team environment.

Ability to follow established guidelines and procedures.

Biostatistician

Knowledge of statistical methods including hypothesis testing, multivariate statistics, and linear regression.

Basic knowledge of experimental design, sampling techniques, and data collection methods.

Skill in data cleaning, transformation, and management.

Ability to explain complex statistical concepts to non-statisticians.

Senior Biostatistician

Knowledge of complex statistical techniques and models.

Advanced knowledge of experimental design, sampling techniques, and data collection methods.

Ability to apply both standard statistical methods and to modify existing techniques to meet project goals.

Advanced skills in statistical programming languages (e.g., R, SAS, Python).

MINIMUM EDUCATION QUALIFICATION

Associate Biostatistician

Bachelor’s degree in statistics, biostatistics, mathematics, or related field with at least 9 units of coursework in statistics. Progressively responsible professional work experience may be substituted on a year-for-year basis for college education.

Biostatistician and Senior Biostatistician

Master’s degree in statistics, biostatistics, epidemiology, demography, or closely related field. Progressively responsible professional work experience may be substituted on a year-for-year basis for college education.

**Minimum Experience Qualification**

Associate Biostatistician

Non-supervisory - No experience necessary.

Biostatistician

Non-supervisory - Two (2) years of experience in statistical analysis and data management. An equivalent combination of relevant education and/or training may be substituted for experience.

Contributing authorship in two (2) significant reports or publications in a public health-related field.

AND

Three (3) presentations at public health-related meetings or conferences in the past three (3) years.

Senior Biostatistician

Non-supervisory – Five (5) years of experience in statistical analysis, data management and data visualization. An equivalent combination of relevant education and/or training may be substituted for experience.

Contributing authorship in at least four (4) significant reports or publications.

AND

Five (5) presentations at public health-related meetings or conferences in the last three (3) years.

AND

Supervisory - Two (2) years involving employee supervision.

MINIMUM CERTIFICATION QUALIFICATION

N/A

**Preferred Education Qualification**

Senior Biostatistician

PhD in biostatistics, epidemiology or closely related field.

**Preferred Experience Qualification**

N/A

**Preferred Certification Qualification**

N/A

**Additional Requirements**

All

Travels occasionally within Alaska in small, fixed wing aircraft; travels outside Alaska.

According to the needs of the organization, some incumbents in this job class may be required to obtain additional specific technical certifications.

At Prolaio, we want to help patients live full and satisfying lives, to prevent and control their illnesses, to give them and their care teams information that can improve their well-being and shape effective care choices.

Our founders are experts in cardiovascular medicine and science. They saw that making new treatments isn’t enough. We need to rethink how care is delivered, so that every patient gets the treatment they need at the right time.

Hearts work on their own times. Not on appointment times. Having a doctor’s appointment once every 3-6 months means missing all the signals that could be happening in between. A connected platform can solve this problem.

We envision a future where patients are seen when they need to be seen, and not when they don’t. They get the care they need, like medication changes, without going to the hospital. Doctors and hospitals get more efficient, the system saves money, and patients live better. This is precision cardiology, and we know it’s within reach.

Industry: Technology, Information and Internet
Company Size: 11-50 employees

Prolaio

Who Are We?

Prolaio believes that continuous learning and collaboration can make a significant difference in how heart care is administered. We are creating smarter ways to address heart disease and heart risks by uniting patients, care teams, and researchers on a secure, technology-enabled platform that drives clinical innovation and offers a path towards better patient outcomes.

This is precision cardiology, and we know it’s within reach.

What Will You Do?

**The Overview **

The Senior Data Scientist, Clinical will leverage advanced data science methodologies to advance the science and clinical applications of digital biomarkers. This role involves developing rigorous technical plans and executing complex analyses on multimodal datasets (digital biomarkers from wearable data, electronic health records [EHR], claims) for publication in high-impact medical journals. The successful candidate will build pipelines to prepare analytic datasets from wearable data and EHR and utilize Python and/or R to develop multimodal risk prediction models to describe, predict, and estimate clinical effects.

**The Specifics **

- **Clinical Analysis & Publication **: Design and execute statistical analyses on large clinical datasets. Author abstracts, statistical analysis plans, conference presentations, and manuscripts for publication in peer-reviewed medical journals.

- **Data Pipeline Development: ** Build, document, and maintain reproducible data pipelines to curate analytic datasets, combining data from multiple assets (e.g., continuous signal data, claims, electronic health records, etc.).

- **Risk Prediction Modeling **: Develop and deploy time-varying and multimodal risk prediction models which extract insights from contextual health data and physiologic signals

- **Scientific Leadership **: Contribute to rigorous science that expands our understanding of digital biomarkers and clinical endpoints in cardiovascular disease in order to enable Prolaio’s ability to support clinical research and cardiovascular care.

- **Cross-Functional Collaboration **: Collaborate cross-functionally with data engineering, operations, clinical, and other teams to ensure data analyses and modeling pipelines align with cross-team standards, scientific validity and company objectives.

- **Advanced Data Abstraction **: Utilize both traditional programmatic and (where applicable) modern LLM-based techniques for complex data processing and clinical abstraction.

**Why Prolaio? **

- **Impactful Work: ** You will join in the fight against heart failure (HF) and hypertrophic cardiomyopathy (HCM) with the goal of extending and saving the lives of our patients while also being at the forefront of changing the healthcare industry through technology.

- **Innovative Environment: ** You will be part of an organization doing something that’s never been done before.

- **Professional Growth: ** You will join a growing team and have a substantial impact on our daily and future operations with the opportunity to continuously learn and grow.

- **Collaborative Team: ** You will be part of a team of collaborative, curious, and committed individuals focused on the collective good, inclusiveness, scientific excellence, and advancing digital health for cardiology.

**Who You Are? **

- **Education & Experience: ** PhD, MD, or master’s degree. 3+ years of academic or industry experience post-PhD/MD or 5+ years post-master’s in any of the following fields: applied statistics, biostatistics, epidemiology, health economics, data science, health informatics, or a related field.

- **Scientific Track Record: ** A strong track record of peer-reviewed scientific publications, with experience communicating scientific results through presentations, abstracts, and manuscripts.

- **Healthcare Data Expertise: ** Experience preparing and analyzing large healthcare data sets, such as claims, electronic health records, or clinical trials. Experience with the specification of clinical event definitions and familiarity with healthcare data standards/ontologies (e.g., FHIR, OMOP, ICD-10, CPT).

- **Time-Series Data: ** Experience processing and analyzing high-volume time-series data.

- **Technical Proficiency: ** Experience in Python for machine learning and pipeline development. Experience in R for biostatistical inference is a plus.

- **Core Expertise: ** Deep expertise in at least TWO or more of the following three areas:

- **Agentic LLMs: ** Experience designing and validating LLM-based agentic pipelines (e.g., with LangChain, Vertex AI, etc.). Experience fine-tuning LLMs is a plus.

- **Machine learning for multimodal data **: Completed projects in Python to develop predictive health risk models using common data sciences libraries (e.g., scikit-learn, etc.) and completed projects utilizing deep learning frameworks (e.g., PyTorch, Jax) for time-series, computer vision, or multimodal data.

- **Biostatistics & Epidemiology **: Proven ability to implement models for statistical inference, with specific expertise in longitudinal health data, time-to-event (survival) analysis, and disease trajectories. Deep understanding of epidemiologic concepts (bias, confounding, data missingness) and familiarity with study design for observational studies and randomized controlled trials.

- **Tools for data science **: Familiarity with modern coding standards for data science including reproducible environment management (e.g. poetry, uv, renv), version control (Git), robust documentation, report generation (e.g. Quarto), and SQL. Experience with production tools for continuous integration, deployment, and experiment tracking (e.g. MLflow and metaflow)

- **Communication **: Ability to work cross-functionally and seamlessly translate highly technical concepts to non-technical audiences and stakeholders.

**Additional Qualifications (Nice to Haves) **

- Prior research or industry experience in cardiovascular disease (CVD) or digital cardiology.

- Prior experience with data from wearables or other sensor data.

**Why You’ll Love Working Here **

- **Meaningful Compensation **: Competitive salary, performance bonus, and equity so you can share in what we build.

- **Great Health Coverage: ** Medical, dental, and vision plans with multiple options and strong company contributions.

- **Flexible Spending Perks: ** HSA, FSA, commuter benefits, and a $1,200 annual Lifestyle Spending Account to support wellness, commuting, family needs, and more.

- **Time to Recharge: ** Generous paid time off, sick leave, and company holidays.

- **Family-First Benefits **: Paid parental leave, caregiver leave, and support for growing families.

- **Security & Peace of Mind **: Company-paid life insurance and short- and long-term disability coverage.

- **Plan for the Future **: 401(k) plan to help you build long-term financial security.

- **Care When You Need It: ** Easy access to telehealth and optional supplemental coverage for life’s unexpected moments.

Starting Salary is at $136,000.00 (Exact Compensation may vary based on skills, experience, and location)

Sr. Data Scientist, Clinical

NextGen is an award-winning IT solutions and services provider. NextGen is a fast-growing company that employs agile and mature processes in areas of innovation, research and development, program management, systems engineering, and technology commercialization. Current customers include the Department of Defense, Federal Government, and commercial companies.

NextGen utilizes a mixed model consisting of Services and Solution Development in support of customer goals. Our core areas of expertise include Software Development, Research and Development, Enterprise IT Systems Engineering, and Cyber Security & Data Management. NextGen obtained ISO 9001 certification and achieved CMMI-DEV and CMMI-SVC Level 3 appraisal. Recent and steady growth led to our recognition by INC 5000 as the 211th (2016), 440th (2017), 1096th (2018), 1703rd (2019), and 2437th (2020) fastest-growing company in the US and 19th fastest growing IT Services Company in the US. NextGen has offices near Aberdeen, MD; Ft. Meade, MD; Dayton, OH; O’Fallon, IL, and Morgantown, WV. 

We understand the paradigm shift of doing more with less; developing, operating, and supporting complex systems and missions while keeping pace with changing technologies; and providing high-quality working solutions to analysts and warfighters supporting the Federal Government. We aggressively manage internal costs to ensure competitive salaries for top talent while ensuring cost-effective delivery to our customers. As the demand for quality increases, NextGen is well-positioned to tackle the most intricate challenges facing the defense and intelligence communities today.

Industry: IT Services and IT Consulting
Company Size: 201-500 employees

NextGen Federal Systems

NextGen Federal Systems, LLC (NextGen) is seeking a Senior Statistician to work on our Operational Analysis Support contract in the 618th Air Operations Center at Scott AFB. Our customer requires a proven senior statistician with a wide variety of industry knowledge and application experience. Successful candidates will employ modern statistical tools and innovation to drive customer savings and efficiencies. Applicants should possess a unique ability to design and implement studies directly applicable to customer focus areas.

**Primary Work Location: **Scott AFB IL

**Position Requirements**

- Extensive experience in statistical analysis, including quantitative and qualitative methods.

- Experience in the development of predictive analysis tools and reports

- Experience in the use of linear programming, operations research, principal component analysis, cluster analysis, univariate and multivariate regression analysis, reliability, and time-series analysis methods to form predictive models for specific response variables

- Secret Clearance or the ability to obtain a clearance.

**Education: ** Master’s degree or equivalent experience in Statistics or Operations Research

**Desired Skills**

- Advanced skills in Excel, including complex formulas and Cognos Report Studio/Framework Manager, VBA, JMP, MATLAB, Minitab, R, SAS, and BI tools/frameworks

About NextGen:

NextGen Federal Systems is an innovative technology and professional services provider specializing in advanced software solutions and comprehensive mission and business support services. We work in close collaboration with our Customers to truly understand their business and mission goals. Our approach is to design, build, implement, and manage solutions that measurably improve our client’s organizational performance. We have established and foster a corporate culture where we:

Treat employees with fairness and respect regardless of their position, sexual identity, race, or tenure. Communicate the importance of our mission and our employees’ contributions to it, ensuring they understand how their job role contributes to the greater good. Openly promote and communicate our ideas for change and adaptability. Strive to achieve results as an organization. Hold employees accountable to their commitments and provide incentives that encourage positive and productive behaviors. Value the talents and contributions of our employees as the key factor for our success. Create an environment where people can engage at all levels. Encourage people to take risks and allow them to make mistakes.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities.

Senior Statistician

PepsiCo is a playground for curious people. We invite thinkers, doers, and changemakers to champion innovation, take calculated risks, and challenge the status quo. From executives to team members on the front lines, we’re excited about the future. We take chances. Together, we dare to make the world a better place.
 
Our associates are the magic ingredient. Each of them plays an integral role in helping create deep connections between people and our products. Think about your last group celebration: Chances are, one of our iconic brands was by your side. At PepsiCo, you’re invited to be a part of a global team of innovators who make, move, and sell these products—which are enjoyed by more than 1 billion people a day.
 
A career at PepsiCo means working in a culture where everyone’s welcome. Here, you can dare to be yourself. No matter who you are or where you’re from, you can influence the people around you and the world at large. By showing up, you’ll have the opportunity to learn, develop and grow your skills for the future. Our supportive teams can fuel your professional goals to make a global impact on people and the planet. 

Join us. Dare for Better.

Industry: Food and Beverage Services
Company Size: 10,001+ employees

PepsiCo

**Job Description: **

The candidate will be responsible for developing, reviewing, and providing feedback on study documents, such as protocols and statistical analysis plans, and executing planned data analyses using administrative claims, electronic health record (EHR), and observational registry databases.

They will work closely with project teams to manage timelines and workflows, and to communicate results and updates to internal cross-functional stakeholders

**Key Responsibilities: **

• Support development of and provide critical appraisal of study protocols for research projects using RWD (e.g., medical claims, EHR, and observational registry databases)

• Lead or support development of statistical analysis plans in collaboration with internal stakeholders (e.g., client Biometrics and programming team members)

• Conduct data reviews for primary/secondary data collected to ensure quality and reliability

• Communicate study results with a broader internal cross-functional audience

• Adapt performance metrics and dashboards for RWE projects

• Support preparation of reports and/or publication materials (e.g., abstracts, manuscripts)

• Support cross-functional initiatives to develop and refine internal procedures, workflows, and best practices

**Basic Qualifications **

• Master’s degree in Epidemiology, Biostatistics, Statistics or related discipline from an accredited institution and 4+ years of experience working with a broad range of RWD, in academia, at a contract research organization, or in the biopharmaceutical industry

OR

• Bachelor’s degree in Epidemiology, Biostatistics, Statistics or related discipline from an accredited institution and 6+ years of experience working with a broad range of RWD, in academia, at a contract research organization, or in the biopharmaceutical industry

**Preferred Qualifications: **

• Master’s degree or Doctoral level training in Epidemiology, Biostatistics, Statistics or related discipline from an accredited institution

• 4+ years of oncology research experience highly preferred

• In-depth knowledge of claims-based RWD (e.g., HealthVerity, Optum) and prior experience of using claims-based RWD in oncology research

• Experience working with EHRs (e.g., IQVIA, Flatiron) and registry databases

• Prior experience of using RWD for RWE in regulatory applications, post-marketing studies, and pharmacovigilance

• Experience with external control arm (ECA) methodologies

• In-depth understanding of the principles of epidemiologic research methods and statistical concepts in support of the analyses and demonstrated proficiency in statistical analysis programming languages commonly used in life sciences (e.g., SAS, R)

• Experience in biopharmaceutical industry

• Excellent verbal, written and presentation skills, including the ability to effectively communicate statistical methodology and analysis results

• Ability to work independently and collaboratively in a constantly changing, diverse, and matrix environment

Statistical Programmer

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