SAS Programmer remote jobs - 549 jobs

A leading healthcare AI company based in Chicago is seeking a Machine Learning Engineer/Data Scientist to develop AI solutions that improve patient care. You will design and optimize machine learning models, collaborate with diverse teams, and stay updated on industry innovations. Ideal candidates possess a strong background in machine learning, proficiency in programming languages like Python, and experience with cloud platforms. Join us for a competitive salary and opportunities for personal development and equity participation. #J-18808-Ljbffr

About Us At Selective, we don't just insure uniquely, we employ uniqueness. Selective is a midsized U.S. domestic property and casualty insurance company with a history of strong, consistent financial performance for nearly 100 years. Selective's unique position as both a leading insurance group and an employer of choice is recognized in a wide variety of awards and honors, including listing in Forbes Best Midsize Employers in 2025 and certification as a Great Place to Work in 2025 for the sixth consecutive year. Employees are empowered and encouraged to Be Uniquely You by being their true, unique selves and contributing their diverse talents, experiences, and perspectives to our shared success. Together, we are a high-performing team working to serve our customers responsibly by helping to mitigate loss, keep them safe, and restore their lives and businesses after an insured loss occurs. Applicants must be authorized to work for any employer in the United States. Selective will not sponsor or assume the sponsorship of an employment visa at this time . Overview Responsible for development and maintenance of analytical solutions through applications of Data Mining, Machine Learning, Predictive Modeling, Generative AI and other emerging technologies for current and future business needs. Lead the supervised and unsupervised model development efforts in partnership with business and Information Technology (IT) stakeholders from diverse functional areas. Proactively monitor outcome post installation and report actionable insights. All job duties and responsibilities must be carried out in compliance with applicable legal and regulatory requirements. Note: (For NJ candidates) This role will be located at our future headquarters in Short Hills, N.J. Until the new headquarters is operational, the successful candidate will be offered the ability to work in our Branchville, N.J. location during this interim period. Responsibilities Understand the competitive marketplace, business issues, and data challenges to deliver actionable insights, recommendations, and business processes. Manipulate high-volume, high-dimensionality data from varying sources to highlight patterns, anomalies, relationships, and trends. Perform descriptive and diagnostics analysis to provide actionable insights for a range of business customers via effective visualization. Perform prescriptive analysis seeking for statistical inference providing information that will drive strategic decision making related to marketing, claims and underwriting. Develop predictive models and machine learning solutions to investigate problems, detect patterns and recommend solutions. Work with Information Technology to integrate the model into production environment. Perform model maintenance and post installation monitoring, including performance tracking, model refit/refresh, documentation, and version control. Research and prototype advanced data science techniques like Text Mining, Natural Language Processing (NLP), Image Recognition, Generative AI and Robotic Process Automation (RPA). Research and recommend new data, tools, modeling techniques to enrich analytics solutions in alignment to policy lifecycle. Participate in the broader community to stay current with industry trends including cutting-edge methodology, software, platform and recommend best practices. Qualifications Knowledge and Requirements Professional statistics/quantitative skills. Hands-on experience of solving business problem with various multi variate statistical methods including generalized linear model, survival model, time series, mixed effects model etc. Familiar with the whole life cycle of predictive modeling, including data provision, model development, validation and testing, model deployment. Proficient with manipulating data with enterprise-scale database systems (SQL, SAS). Proficient with at least one scripting language such as R, Python, or Java. Experience with BI tools such as Tableau, Spotfile etc. is preferred. Knowledge of HTML for web app development is preferred. Hands on experience with Big Data / Hadoop / Spark is preferred. Experience with version control workflow such as Git is plus. Education and Experience PhD with 1 year of Predictive Modeling Experience, or Masters with 2-3 years of Predictive Modeling Experience or Bachelors with 4-5 Years of Data Science Experience and education in Statistics, Economics, Computer Science, Mathematics or related field preferred. Property & Casualty Insurance experience highly preferred. Total Rewards Selective Insurance offers a total rewards package that includes a competitive base salary, incentive plan eligibility at all levels, and a wide array of benefits designed to help you and your family stay healthy, achieve your financial goals, and balance the demands of your work and personal life. These benefits include comprehensive health care plans, retirement savings plan with company match, discounted Employee Stock Purchase Program, tuition assistance and reimbursement programs, and 20 days of paid time off. Additional details about our total rewards package can be found by visiting our benefits page. The actual base salary is based on geographic location, and the range is representative of salaries for this role throughout Selective's footprint. Additional considerations include relevant education, qualifications, experience, skills, performance, and business needs. Pay Range USD $97,000.00 - USD $146,000.00 /Yr. Additional Information Selective is an Equal Employment Opportunity employer. That means we respect and value every individual's unique opinions, beliefs, abilities, and perspectives. We are committed to promoting a welcoming culture that celebrates diverse talent, individual identity, different points of view and experiences - and empowers employees to contribute new ideas that support our continued and growing success. Building a highly engaged team is one of our core strategic imperatives, which we believe is enhanced by diversity, equity, and inclusion. We expect and encourage all employees and all of our business partners to embrace, practice, and monitor the attitudes, values, and goals of acceptance; address biases; and foster diversity of viewpoints and opinions. For Massachusetts Applicants It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

- Master's or PhD Preferred! -Agentic AI experience - 5-10+ years of experience in AI and machine learning, model building, evaluation, and fine-tuning. - 2+ years of working knowledge of applying recent LLMs including ChatGPT, GPT 3.5, OPT, BLOOM, etc. UTILIZING RAG! - Experience working directly with large language models and Transformer based architectures including BERT, RoBERTa, T5 etc. - NLP Experience (Named Entity Recognition, Sentiment Analysis, Text Summarization) - Experience with conversational search / semantic search, reinforcement learning, prompt engineering, hallucination mitigation - DevOps repos Debugging, building APIs and managing the algorithm flow across multiple workstreams in one repo - Senior level experience deploying models in the Cloud (AWS) or Azure as secondary. *Description* TEKsystems is partnered with a software company in Raleigh that needs to hire a Senior Data Scientist for their flagship product, a leading global provider of information and analytics. Recently our client has focused on the general availability of their product for U.S. customers, a generative AI solution designed to transform legal work. Our client delivers trusted results in a familiar, easy-to-use interface with linked hallucination-free legal citations that combine the power of generative AI with proprietary search technology, Shepard's Citations functionality, and authoritative content. The Senior Data Scientist will focus on search and be dedicated to the creation of next-generation AI and Machine Learning techniques and strategies for our client in their global expansion. This candidate will assist with deploying ethical, powerful generative AI solutions with a flexible, multi-model approach that prioritizes using the best model for each individual legal use case. This approach includes working with large language models like Anthropic's Claude 2, hosted on Amazon Bedrock from Amazon Web Services (AWS), and OpenAI's GPT-4 and ChatGPT, hosted on Microsoft Azure. ACCOUNTABILITIES * Solve some of the most challenging problems in natural language processing, machine learning, and information retrieval including topical classification, sentiment analysis, user intent detection. * Research, build, and deploy models based on both shallow and deep machine learning. Train robust NLP-based models a very large corpus of news and financial data. * Apply machine learning techniques for improving search algorithms. * Drive best practices for NLP/Machine Learning pipelines. * Maintain current knowledge base of state-of-the-art ML algorithms (BERT, ELMo, GPT, etc.), API's, and open-source methods and be able to quickly evaluate alternatives. * Translate complex business requirements into actionable stories with reasonable time estimates. * Work with product leaders to apply data science solutions. Strong coding skills in Python 7+ years- interviews need to be take without AI assistance Be a natural problem solver, able to take a lead in collaborating to resolve issues Proficiency in IDE debugging : VSCODE and PYCHARM Have communication skills 4+ years of experience in AI and machine learning Deep understanding of machine learning algorithms, classification models, diagnostic testing of models Experience working directly and Transformer based architectures including BERT, RoBERTa, T5 etc. Nd familiarity with large language models and fine tuning Experience with conversational search / semantic search, reinforcement learning, prompt engineering, hallucination mitigation Working understanding of the business risks associated with applying LLM (LangChain) in a business Experience working with AWS, RAG, SageMaker, SQL *Skills* data science, nlp, indexing, semantic search, conversational search, langchain, Generative AI, Large language model, Sql, aws, algorithm, artificial intelligence, Retrieval augmented generation, fine-tuning, Python, Machine learning, cloud computing *Top Skills Details* data science, nlp, indexing, semantic search, conversational search, langchain, Generative AI, Large language model ,Sql, aws, algorithm, artificial intelligence, Retrieval augmented generation, fine-tuning *Additional Skills & Qualifications* N/A *Experience Level* Expert Level *Job Type & Location*This is a Contract to Hire position based out of Cary, NC. *Pay and Benefits*The pay range for this position is $50.00 - $85.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) *Workplace Type*This is a fully remote position. *Application Deadline*This position is anticipated to close on Jan 26, 2026. h4>About TEKsystems: We're partners in transformation. We help clients activate ideas and solutions to take advantage of a new world of opportunity. We are a team of 80,000 strong, working with over 6,000 clients, including 80% of the Fortune 500, across North America, Europe and Asia. As an industry leader in Full-Stack Technology Services, Talent Services, and real-world application, we work with progressive leaders to drive change. That's the power of true partnership. TEKsystems is an Allegis Group company. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. About TEKsystems and TEKsystems Global Services We're a leading provider of business and technology services. We accelerate business transformation for our customers. Our expertise in strategy, design, execution and operations unlocks business value through a range of solutions. We're a team of 80,000 strong, working with over 6,000 customers, including 80% of the Fortune 500 across North America, Europe and Asia, who partner with us for our scale, full-stack capabilities and speed. We're strategic thinkers, hands-on collaborators, helping customers capitalize on change and master the momentum of technology. We're building tomorrow by delivering business outcomes and making positive impacts in our global communities. TEKsystems and TEKsystems Global Services are Allegis Group companies. Learn more at TEKsystems.com. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Our mission is to shape the future of clinical research. With decades of experience and the brightest minds in the industry, we help the global biopharmaceutical industry bring new, advanced medical treatments to market, faster. We seek to change the world, and with the support of our teams across the globe, we flourish together. At Perceptive, we are one team. We learn, grow and win together. Are you ready to help change the world? Apart from job satisfaction, we can offer you: HEALTH: - Medical, Dental and Vision benefits for you and your family, including Flexible Spending Accounts (FSA) and Health Savings Accounts (HSAs) YOURSELF: - Paid time off policy including holidays and sick time - Internal growth and development programs & trainings WEALTH: 401(k) program, life & accident insurance and disability insurance About the role Job Purpose To create databases and exports for sponsor study set ups. Creates integrations between systems as needed. Reviews and performs User Acceptance Testing on programs and configurations as trained. Key Responsibilities Database Builds and Exporting • Develop data collection forms to maximize efficiencies in data acquisition across multiple imaging modalities and therapeutic areas. • Programming data cleaning/consistency checking programs to support internal applications for all therapeutic areas • Programming and testing data export programs in accordance with specific client needs • Design and develop custom calculations, error checks, and automated data validation routines. Build data conversion paths and develop efficient and appropriate sponsor deliverable file formats, including CDISC SDTM and ODM compliance requirements Advise on the development of database quality standards including the oversight of standard eCRF library and version control processes Data Integrations Assist with the development of data integrations for continuity across internal data platforms (sites, sponsors, Perceptive locations) Other Provide coaching, support and mentoring to less experienced team members in data management practices and related technical issues Support Data Management personnel in the development of technical documentation • Carry out any other reasonable duties as requested. Functional Competencies (Technical knowledge/Skills) • Strong documentation and reporting capabilities • Strong written and verbal skills for effectively communicating with departmental staff and research centers Experience implementing CDISC standards Understanding of GxP Understanding of 21 CFR Part 11Entry level SAS programming experience Experience with EDC (e.g. OpenClinica, RAVE, Inform, TrialMaster, etc.) Entry level SQL proficiency• Entry level Javascript proficiency Experience, Education, and Certifications • Bachelor's Degree in mathematics, computer science or equivalent demonstrated technical and analytical experience. • Previous experience in data management role This role is remote. Candidates located in the following states: AZ, CT, DE, FL, GA, IL, MA, MO, NH, NJ, NC, PA, UT, VA are preferred are preferred. The annual base salary range for this role is $51,139- $94,973. This range represents the anticipated initial annual salary and will vary depending on several factors including the candidate's experience and skills as well as market rate adjustment. Come as you are. We're proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, colour, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.

Businesses face challenges every day building responsive and agile IT capabilities to grow and stay ahead. Since everyone has access to the same tools, your competitive advantage directly depends on how you apply technology - on the people leading, supporting and optimizing your IT initiatives. USM Business Systems, established in 1999, is an industry-leading private talent management firm, specializing in providing unique IT turnkey solutions, IT staffing solutions, and Talent management insights, enabling you to sustain a truly competitive advantage in this fast-moving environment. USM has offices throughout the US and offshore delivery centers in India. USM is a certified Minority Business Enterprise and is a CMMi Level 3 Organization. USM is recognized as one of the fastest growing IT Temporary Staffing firms in the US and most recently was ranked #3 on the list of the Top Temporary Staffing firms in the DC Metro Area - Washington Business Journal (2016). SAS Programmer/Analyst 2 month contract Houston, TX Need GC and USC • The candidate will be required to come onsite for the initial portion of the contract, but can work remotely thereafter assuming rapport and communication model is established. • Communication is very important, if communication is not very good they won't get the job. Top Three Skills: (1) 5+ years experience with SAS reporting platform (2) 5+ years experience with SAS/BASE programming (3) 5+ years experience with SQL and Excel SAS Programmer/Data Analyst needed to automate processes to allow for quicker turn-time on recurring analyses and reports. Skillset and experience should include SAS/Base with experience in developing Macros using SAS procedures, ODS for tables and graphs/charts, and custom technology for advanced import/exports from a variety of locations and file types. SAS data management skills and experience is more important that statistical training. • Design and build of a Custom Report/Dashboard that presents metrics and possibly unique visualizations to leverage sourced data and computations. • Design and build of a custom technology component that can be re-used to perform a targeted type of statistical analysis with defined parameters. Job Description: Design and build of a custom technology component that can be re-used to perform a targeted type of statistical analysis with defined parameters. Design and build of a Custom Report/Dashboard that presented metrics and possibly unique visualizations to leveraged sourced data and computations to show. Additional Information If you are interested in the below position please forward your profile to preethib@usmsystems(dot)com or call me on ************.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Candidate to provide statistical programming support and validation and help set specifications of analysis datasets, pooled datasets, statistical tables, summaries, figures and listing for Phase II-IV clinical trials. Employ standardized programs where applicable. Provide input into planning documents such as protocol, validation plan, and report analysis plan. Provide outputs for clinical study reports, integrated summaries and electronic submissions. Help respond to health authority inquiries for submitted dossiers. Establish and maintain sound working relationship and effective communications within biostatistics and statistical reporting and clinical research. Skills: Min 2-3 years of programming experience in HARP, the GSK programming environment is required. At least 8 years work experience in a Statistical (SAS) programming role preferably supporting clinical trials or in the pharmaceutical industry (5 years for Masters in Mathematics, Statistics/Computer Science or health science graduates). Advanced knowledge of / experience with SAS and other relevant programming software. Proven experience in development of advanced MACROs with high programming efficiency; strong programming and problem-solving skills. Proven experience in leading programmer support for multiple clinical trials and submission activities (or equivalent). Expertise in programming according to specifications of analysis datasets, pooled datasets, listings, tables and figures for clinical trials and submission activities. Working knowledge of database design/structures and basic statistics. Working experience in pooling analysis datasets across multiple clinical studies (or equivalent). Good understanding of global clinical trial/project practices, procedures, methodologies. Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH). Oncology experience preferred Strong expertise in CDISC on the submission bucket including CRT programming will be a definite plus. Intermediate knowledge of office tools Fluent English (oral and written) Excellent in people interaction and be a collaborative team player. Qualifications Must have a BA/BS or equivalent experience in computer science, mathematics, statistics, life sciences, or related field(s). Additional Information Regards, Akriti Gupta Associate Recruiter(Scientific & Clinical Division) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter

You will contribute by: Providing support to the Epidemiology team by preparing Real World data, advising on data analytic strategies, and supporting stakeholders in various epidemiology analytic activities Programming and conducting statistical analysis under the direction and supervision of epidemiologists/statisticians including data coding, creation of algorithms, linkage of datasets, and use of statistical packages or platforms Supporting statistical programming to generate innovative means of data standardization, visualization, and reporting of observational data Supporting Medical Affairs (e.g. observational studies leveraging RWD); Global Patient Safety and Risk Management (e.g., analysis to obtain background rates) for the development of regulatory/safety documents, and Clinical Development (e.g.; assessment of patient populations/ protocol feasibility) The position will partner with Epidemiologists to manage relationships with internal and external stakeholders Being able to prioritize and manage work across multiple projects and stakeholders Providing strong communication to ensure successful and timely project delivery Solving technical problems with experience and expertise What we're looking for: Master's degree or PhD in related field (epidemiology, biostatistics, statistics, bioinformatics, economics) and 5+ years of experience conducting RWE analytics for pharma industry, CRO, or academic institution Intermediate to expert level proficiency in SQL is a must. In addition, SAS or R proficiency is required Deep expertise analyzing RWE data sources such as Optum (Clinformatics Datamart and Market Clarity), Truveta and UK Biobank. Experience analyzing clinical trial and/or registry data is desirable Familiarity with relational databases and proficient understanding of claims and ancillary file layouts Experience with applied statistics including regression analysis (OLS, longitudinal, logistic, Cox, GLM/GEE), survival analyses (Kaplan-Meier, cumulative incidence, accelerated failure time models), and propensity weighting Excellent project management skills; can prioritize multiple tasks and goals to ensure timely completion Confident and competent when interacting with internal and external stakeholders Strong written/verbal communication skills. Highly effective at summarizing and presenting key considerations and evidence Summary of Key Responsibilities: Assist in development of study protocols and analysis plans leveraging large RWD sources (Claims and/or EHR) Liaise with data vendors to obtain relevant data extracts for research studies consistent with study protocols Create analytical databases from data extracts to facilitate conduct of data analyses Conduct analyses consistent with methods set forth in study protocols and analysis plans Produce tables and figures for discussions with other investigators, clients, and for study reports Present results internally and to clients Assist in the preparation of study reports and other deliverables May have supervisory responsibilities in the future

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today. Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest's headquarters are located in Markham Ontario, Canada with additional locations in: Bridgewater, New Jersey; Shanghai, China; Taipei, Taiwan; and multiple offices in Europe. Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients' needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success. Quality is our backbone, customer-focus is our tradition, flexibility is our strength…that's us…that's Everest. To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as FSP Principal Statistical Programmer for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy. Key Accountabilities: Lead projects with higher level of complexity/challenges/difficulties. Lead efforts to resolve complex statistical programming issues or problems. Perform a leadership role in statistical programming projects by coordinating study team(s), overseeing timelines, assigning and following up on programming tasks, interacting with clients, and ensuring quality of programming deliverables. Assist statistical programming management in properly planning and allocating resources based on timelines, statistical programmers' skills and expertise, as well as availability. Participate in developing and maintaining clinical trial data and statistical programming standards to ensure the company standards are up to date and in line with pharmaceutical industry standards, conventions, and regulatory requirements. Perform hands on primary statistical programming and validation programming on assigned projects including but not limited to phase I - IV clinical trials, integrated clinical summaries, responses to requests from regulatory agencies, publication support, data explorations, data monitoring committee meetings, etc. Create SDTM mapping specifications and ADaM data specifications. Perform quality control (QC) review of these documents prepared by others. Create SDTM and ADaM define.xml files. Perform QC review of these files prepared by others. Perform 3rd level QC review on programming deliverables before their release to the clients. Perform QC review/assessment on regulatory submission programming documents, datasets, tables/listings/graphs (TLGs), and computer programs, etc. May lead programming efforts for drug development programs or for assigned client clusters. Provide training, mentorship, and technical guidance to less experienced Statistical Programmers or Biostatisticians who perform statistical programming. Monitor the compliance and adherence to the established data and programming standards, and statistical programming governing documents. May represent the company in interactions with clinical trial sponsors with regard to statistical programming projects and relevant businesses. Participate in the development of statistical programming policies, SOPs, guidelines, and good working practices. Participate in statistical programming project bidding or bid defense meetings. Work with document management specialists/archivists to plan and perform archival of the statistical programming datasets, outputs, documents, and final programs upon the completion of the assigned projects. Perform transfer of the archived files to the clinical trial sponsors. Qualifications and Experience: M.Sc., M.A. or higher degree in Statistics, Biostatistics, Computer Science, or relevant fields. 10 (M.Sc., M.A.)/9 (Ph.D.) years' related experience. An in-depth knowledge of clinical trial data processing and manipulation, hands on statistical programming and analysis, requirements for assembling and presenting trial results to regulatory agencies. Knowledge of industry standards on how clinical trial data are structured, stored, analyzed, and presented. Knowledge of clinical trial regulatory and ICH requirements. Must demonstrate ability to effectively plan, control, and carry on tasks in SAS programming, statistical analysis, and submission of trial data and results to regulatory agencies. Must possess in-depth level understanding of the concept of standardization in data, programming, and statistical reporting of trial results, and its implication to the relevant functions and operations. Must have sound technical judgment and experience in process design and implementation in relevant areas. Strong leadership and drive to achieve goals will be required. To find out more about Everest Clinical Research and to review other opportunities, please visit our website at **************** Estimated Salary Range: $125,000 - $155,000. We thank all interested applicants, however, only those selected for an interview will be contacted. Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process. #INDHP

Remote Principal Statistical Programmer needs 10 years Pharmaceutical/Biotech programming experience including macro/tools development experience. Remote Principal Statistical Programmer requires: Minimum 10 years Pharmaceutical/Biotech programming experience including macro/tools development experience. FDA submission experience is highly desirable. Strong SAS programming and Statistical background with strong skills in SAS Base, SAS/Macros, SAS/Graph and SAS/Stat. Ability to use professional concepts to achieve objectives in creative and effective ways. Experienced in managing multiple projects. Solid knowledge of SAS Programming language, Software Development Life Cycle and CDISC standards (SDTM & ADaM). Solid knowledge of other software such as SpotFire, R Shiny etc. is a plus. BS/MS in Statistics, Math or Scientific Discipline. Remote Principal Statistical Programmer duties: Lead on clinical studies and integrated analyses and provide guidance and training to other lower level personnel. Develop or evaluate software tools, SAS macros, utilities to automate programming activities and support Biometrics team collaboration. Contribute and implement to statistical analysis plans; provide additional expertise in the analysis of clinical trial when it relates to protocol development, case report form design and data collection. Review Data Management Plan, Data Transfer Plan, Data Validation Plan and Edit Check Specifications and provide comments. Work closely with Biostatistics to create analysis specifications following the instructions provided in Statistical Analysis Plan (SAP). Create CDISC SDTM and ADaM files, SAS export files, Define.xml and Reviewer's Guide for Electronic Submission.

This opportunity is only for candidates currently residing in the specified country. Your location may affect eligibility and rates. Please submit your resume in English and indicate your level of English. At Mindrift, innovation meets opportunity. We believe in using the power of collective intelligence to ethically shape the future of AI. What we do The Mindrift platform connects specialists with AI projects from major tech innovators. Our mission is to unlock the potential of Generative AI by tapping into real-world expertise from across the globe. About the Role GenAI models are improving very quickly, and one of our goals is to make them capable of addressing specialized questions and achieving complex reasoning skills. If you join the platform as an AI Tutor in Statistics, you'll have the opportunity to collaborate on these projects. Although every project is unique, you might typically: Generate prompts that challenge AI. Define comprehensive scoring criteria to evaluate the accuracy of the AI's answers. Correct the model's responses based on your domain-specific knowledge. How to get started Simply apply to this post, qualify, and get the chance to contribute to projects aligned with your skills, on your own schedule. From creating training prompts to refining model responses, you'll help shape the future of AI while ensuring technology benefits everyone. Effort estimate Tasks for this project are estimated to take 6-10 hours to complete, depending on complexity. This is an estimate and not a schedule requirement; you choose when and how to work. Tasks must be submitted by the deadline and meet the listed acceptance criteria to be accepted. Requirements You hold a Bachelor's, Master's or PhD Degree in Statistics, Biostatistics, Econometrics and/or in a relevant area. You have professional experience in one of the following fields: Applied Statistics, Bayesian Statistics, Biostatistics, Econometrics, Economic Statistics, Experimental Design (DOE) & A/B Testing, Generalized Linear Models (GLMs), Hypothesis Testing, Machine Learning (e.g., Classification, Regression, Clustering), Probability Theory, Statistical Modeling, Time Series Analysis. Your level of English is advanced (C1) or above. Expertise in statistical modeling and data analysis, including areas such as descriptive and inferential statistics, regression analysis, experimental design, and machine learning. Proficiency in Python, with experience using libraries such as Pandas, NumPy, SciPy, Statsmodels, and Scikit-learn. Strong ability to design creative and diverse problems, particularly those that are computationally intensive and go beyond simple parameter modifications. You are ready to learn new methods, able to switch between tasks and topics quickly and sometimes work with challenging, complex guidelines. Our freelance role is fully remote so, you just need a laptop, internet connection, time available and enthusiasm to take on a challenge. Benefits Why this freelance opportunity might be a great fit for you? Get paid for your expertise, with rates that can go up to $73/hour depending on your skills, experience, and project needs. Take part in a part-time, remote, freelance project that fits around your primary professional or academic commitments. Work on advanced AI projects and gain valuable experience that enhances your portfolio. Influence how future AI models understand and communicate in your field of expertise.

Handshake is recruiting Statistician Professionals to contribute to an hourly, temporary AI research project-but there's no AI experience needed. In this program, you'll leverage your professional experience to evaluate what AI models produce in your field, assess content related to your field of work, and deliver clear, structured feedback that strengthens the model's understanding of your workplace tasks and language. The Handshake AI opportunity runs year-round, with project opportunities opening periodically across different areas of expertise. Details The position is remote and asynchronous; work independently from wherever you are. The hours are flexible, with no minimum commitment, but most average 5-20 hrs The work includes developing prompts for AI models that reflect your field, and then evaluating responses. You'll learn new skills and contribute to how AI is used in your field Your placement into a project will be dependent on project availability-if you apply now and can't work on this project, more will be available soon. Qualifications You have at least 4 years of professional experience in one or more of the following types of work. The examples below reflect the types of real-world responsibilities that you might have had in your role that will give you the context needed to evaluate and train high-quality AI models Analyzing and interpreting statistical data to identify significant differences and relationships among sources of information. Evaluating statistical methods and procedures used to obtain data to ensure validity, efficiency, and accuracy. Reporting results of statistical analyses, including information presented as graphs, charts, and tables. Determining whether statistical methods are appropriate based on user needs or research objectives. Preparing data for processing by organizing, cleaning, and weighting raw datasets. Developing and testing experimental designs, sampling techniques, and analytical methods. Identifying relationships and trends in data, as well as factors influencing research outcomes. Presenting statistical and nonstatistical results using visual aids such as charts and graphs for diverse audiences. Designing research projects that apply valid scientific techniques using baseline or historical data to structure efficient analyses. Adapting statistical methods to solve domain-specific problems in areas such as economics, biology, healthcare, or engineering. Evaluating data sources to determine limitations regarding reliability and usability. Processing large datasets for statistical modeling and graphic analysis using specialized software or programming languages. Developing custom software applications or scripts for statistical modeling and visualization. Reporting research findings in peer-reviewed papers, technical documentation, or internal reports. Planning data collection methods and determining appropriate sample types and sizes for specific projects. Applying sampling techniques or using complete enumeration bases to define survey groups. Examining theoretical foundations such as probability and inference to develop or refine methods for obtaining and evaluating data. Supervising and training workers responsible for collecting and tabulating data. Preparing and structuring data warehouses for efficient data storage and retrieval. You're able to participate in asynchronous work in partnership with leading AI labs. Application Process Create a Handshake account Upload your resume and verify your identity Get matched and onboarded into relevant projects Start working and earning Work authorization information F-1 students who are eligible for CPT or OPT may be eligible for projects on Handshake AI. Work with your Designated School Official to determine your eligibility. If your school requires a CPT course, Handshake AI may not meet your school's requirements. STEM OPT is not supported. See our Help Center article for more information on what types of work authorizations are supported on Handshake AI. #indhp

9th Way Insignia is a service-disabled, veteran-owned small business bringing transformative technology to our government customers so they can achieve their missions. Our specialties include cybersecurity, cloud modernization, software development, data analytics, enterprise architecture, enterprise IT, analytics, process automation, and artificial intelligence. Learn more about 9th Way Insignia at **************************** Application password: Niner 9 th Way Insignia provides business intelligence and analytics solutions to meet a range of needs from basic data integration, business analytics, and intuitive graphical analyses, to AI and machine learning tools that develop advanced statistical models on both structured and unstructured data. Our software and business intelligence designs include identifying and developing opportunities to eliminate the need to perform repetitive, simple activities through use of bots, or to enhance and improve user experience with chatbots or intuitive, data-driven prompts that improve quality and reduce user stress. Data science Data platform design Big data architecture Data visualization Machine learning (ML) Robotic process automation (RPA) Natural language processing (NLP) Latent semantic indexing (LSI) Statistical modeling and algorithm development 9th Way Insignia's range for this job level is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law. Clearance/Background Investigation Applicants selected will be subject to a security investigation and may need to meet eligibility requirements for access to classified information. Benefits Eligible employees will have access to our comprehensive benefits package which includes Medical, Dental, Vision, Voluntary Life Insurance, 401(k), Basic Life A&D, STD, LTD, PTO, Telehealth, paid holidays, FSA, HSA. Additional resources include our Employee Assistance Program (EAP) and Traveling Assistance. Legal We're an equal employment opportunity employer that empowers our people to fearlessly drive change - no matter their race, color, religion, sex (including pregnancy, childbirth, lactation, or related medical conditions), national origin, age, marital status, sexual orientation, gender identity, disability, veteran status, military or uniformed service member status, genetic information, or any other status protected by applicable federal, state, or local law.

All JerseySTEM roles are pro-bono (unpaid) positions. JerseySTEM is a mission-driven professional network of pro-bono contributors dedicated to improving access to STEM education and career pathways for underserved middle school girls in New Jersey. Members contribute their professional skills and leverage their networks in service of the organization's gender-equity agenda. Membership is a minimum six-month commitment of approximately six flexible hours per week and includes a $100 refundable deposit, returned after six months of active membership. K-12 educators, retirees, veterans, interns, and students are exempt from the deposit. Overview This is a pro-bono volunteer position. JerseySTEM is looking for talented professionals across our departments to commit time and energy as long-term engagement for our mission to provide STEM education to underrepresented middle school girls. The Staff Analytics Team Lead will lead and manage the team, analyze data, and generate insights to optimize staff performance and workforce planning and enhance organizational efficiency through data-driven decision-making. Responsibilities Lead and manage the Staff Analytics team, providing direction, guidance, and support in data analysis and reporting. Collaborate with HR and other departments to identify key metrics and data requirements for workforce planning and decision-making. Design and implement data collection processes and systems to ensure accurate and reliable data. Analyze and interpret data to generate insights and recommendations for improving staff performance and organizational efficiency. Prepare and present reports and dashboards to senior management and stakeholders. Stay up-to-date with industry trends and best practices in data analytics and workforce management. Qualifications Bachelor's or Master's degree in Data Science, Statistics, Business Analytics, or a related field. Proven experience in data analytics and reporting, preferably in a leadership role. Strong analytical and problem-solving skills, with the ability to interpret complex data sets. Proficiency in data analysis tools and software such as Excel, SQL, Python, or R. Excellent communication and presentation skills. Leadership and team management abilities. Detail-oriented and able to handle multiple projects simultaneously. Data-driven mindset with a focus on delivering actionable insights.

Job Description: Work Time Zone: Eastern Time Zone (EST) Employment Type: 12-month contract (renewable) Please NOTE: This role requires over 8 years of hands-on SAS programming experience and expertise in Tableau within the pharmaceutical and biotech industry. Key Qualifications: - Tableau Expertise: At least 4+ years of experience in creating, managing, and optimizing dashboards, reports, and visualizations in clinical trial data contexts. - SAS Programming: Over 8 years of industry experience working with clinical trial data as a SAS/Statistical Programmer. - Oncology Experience: 4-5 years of experience in oncology-focused clinical trials and overseeing CRO activities. - Data Visualization: Recent experience in producing data visualizations using Tableau, such as real-time data review dashboards. - Study Setup and Analysis: Experience in setting up studies and generating visualizations using Tableau, preprocessing clinical data using SAS, assessing the quality of analysis data, and performing cross-study analyses. - Collaboration: Strong collaboration skills with staff in Biostatistics, Clinical Data Management, Clinical Research, and Global Drug Safety. - Programming Support: Ability to provide programming support for generating tables, listings, and figures for assigned projects. - CDISC Standards: Knowledge and application of CDISC standards (SDTM, ADaM) to submission activities. - Validation: Experience in creating and validating safety tables, efficacy tables, and lab shift tables in line with SAP and mock layouts and validating datasets and outputs through double programming. - Process Improvement: Participation in process improvement initiatives, internal programming tasks, and presentations to internal committees and boards. Required Skills, Experience, and Education: - A master's or bachelor's degree (or equivalent qualification) in a relevant field or 10 years of industry experience. - 4+ years of expertise in Tableau (mandatory). - 8+ years of experience in statistical programming with clinical trial data, particularly using SAS software. - Strong communication and collaboration skills, with a proven ability to thrive in a multidisciplinary team environment. - Prior experience in oncology-focused clinical trials is preferred. - Exceptional time management and organizational abilities to meet deadlines and deliver high-quality results. Required Skills: Tableau

Diné Development Corporation (DDC) is a Navajo Nation owned family of companies that delivers IT, professional, and environmental solutions to advance the missions of federal, state, and tribal government agencies. As thought leaders and innovators, our team of specialists build client-centric solutions that solve critical challenges faced by defense, civilian, and healthcare organizations. Employing a mission-focused approach, we deliver value that not only enhances current operations, but also drives future change. Closely aligned with this approach is our commitment to advancing the Navajo Nation and its People. Through economic development and community empowerment, we elevate the Navajo Nation to provide lasting impact and sustainable growth for future generations. DDC's ability to unite legacy-inspired technologies, industry best practices, and proven methodologies has contributed to our success for twenty years. Job Duties and Responsibilities: Provide planning, which includes development of implementation and installa-tion plans for IBM Mainframe projects. The implementation plan should in-clude: detailed steps and requirements to successfully implement OS's, software or hardware upgrades, or installations to IBM System z/OS mainframe platform. Develop timelines and milestones related to the required steps for implementa-tion or upgrade of IBM mainframe platform to meet government established project deadlines. Use required software tools, including IBM SMP/e, IBM system utilities (including IEBGENER (generalized copy utility), IEBCOPY (utility to copy, compress, merge partitioned data sets), IDCAMS (access method services)), to create, populate, update and configure required datasets and parameter libraries and members to successfully implement software installations and upgrades on the IBM mainframe platform. Create and deliver detailed installation/upgrade documentation, using government specified software and processes and formats. This documentation will include detailed dataset names, configuration parameters, and installation/upgrade procedures used to install/upgrade the IBM mainframe OS, software or hardware. Use IBM SMP/e to successfully receive and apply z/OS communications or networking software and other related software on an IBM Mainframe. This includes interpreting SMP/e output messages to resolve software installation issues and requirements, use SMP/e panels to manage software installation packages, define SMP/e required parameters to successfully install and maintain OS and associated software products. Create, define and manage parameters required for communications products on the IBM Mainframe platform. This includes VTAM, VPS (Virtual Print Services), NDM, TCP/IP, FTP, SFTP, and other government approved communications, printer, or networking software or hardware. Diagnose and resolve IBM z/OS system communications software or hardware abends and abnormal operating environment problems using system logs, and other available logs and documents. This includes creating and interpreting system traces and dumps, job output, and monitoring tools. Create, populate, secure and troubleshoot IBM z/OS USS file systems and mount points. Manage the USS environment on an IBM z/OS mainframe platform. Create/update and debug z/OS parameters using government processes and procedures and requirements (aka PARMLIB). Plan and create accurate, detailed documentation for IBM z/OS mainframe platform communications and networking software/hardware installation/upgrades. Use IBM z/OS mainframe communications products, including VTAM, TCP/IP, and FTP. Create, update, and debug JES2 parameters and statements that relate to IBM mainframe networking or communications. (NJE, RJE, NODES statements) Job Requirements (Education/Skills/Experience): Must possess an Active Secret Clearance or be eligible to obtain Must currently possess one of the IAT Level 1 certification: A+CE CCNA-Security Network+ CE SSCP This contractor and subcontractor shall abide by the requirements of 41 CFR 60-1.4(a), 60-300.5(a) and 60-741.5(a). These regulations prohibit discrimination against qualified individuals based on their status as protected veterans or individuals with disabilities, and prohibit discrimination against all individuals based on their race, color, religion, sex, sexual orientation, gender identity, national origin, or for inquiring about, discussing, or disclosing information about compensation, or any other basis prohibited by law. We participate in E-Verify.

What You'll Do: The Senior Statistical Programmer generates tables, listings and graphs to support statistical analyses of data for clinical studies, regulatory submissions and publications. This position requires a good understanding and ability to provide datasets using current industry standards including Clinical Data Interchange Standards Consortium (CDISC) Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM). Review key study documents produced by other functions (protocols, statistical analysis plans [SAPs], TFL shells, case report forms) and interact with Statisticians and other clinical team members to ensure programming requirements are understood. Follow SAPs, develop specifications and execute derivation algorithms for analysis dataset production. Follow the SDTM and ADaM Implementation Guide to develop specifications, create programs to produce CDISC-compliant SDTM and ADaM datasets and define.xml files. Generate tables, figures, and listings, (TFLs) in accordance with the SAP and TFL shells to support analyses using Base SAS, SAS Macro, SAS/STAT, SAS/GRAPH, or other statistical graphics technology. Create and maintain integrated analysis datasets including closed and ongoing studies. Validate SAS programs, macros, datasets, and TFL output generated by other Programmers. Develop or assist in the development of departmental processes and procedures. Other duties as assigned. How You'll Get There: Experience working in Pharmaceutical/ Biotechnology/CRO industry as a Statistical Programmer is required (>= 3 years with MS degree; >=5 years with BS degree). High proficiency in SAS programming and Macro development Experience working with CDISC SDTM and ADaM compliant data sets Experience with regulatory submissions and creating Define.XML. Knowledge of statistics and the drug development process In-depth knowledge of FDA/ICH guidelines and industry/technology standard practices Knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs Capable of critical thinking and independently identifying issues in existing programs Solid verbal and written communication skills Bachelor's /Master's Degree in Statistics, Mathematics, Computer Science, or other related discipline is required; Master's degree is preferred

What You'll Do: The Senior Statistical Programmer generates tables, listings and graphs to support statistical analyses of data for clinical studies, regulatory submissions and publications. This position requires a good understanding and ability to provide datasets using current industry standards including Clinical Data Interchange Standards Consortium (CDISC) Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM). Review key study documents produced by other functions (protocols, statistical analysis plans [SAPs], TFL shells, case report forms) and interact with Statisticians and other clinical team members to ensure programming requirements are understood. Follow SAPs, develop specifications and execute derivation algorithms for analysis dataset production. Follow the SDTM and ADaM Implementation Guide to develop specifications, create programs to produce CDISC-compliant SDTM and ADaM datasets and define.xml files. Generate tables, figures, and listings, (TFLs) in accordance with the SAP and TFL shells to support analyses using Base SAS, SAS Macro, SAS/STAT, SAS/GRAPH, or other statistical graphics technology. Create and maintain integrated analysis datasets including closed and ongoing studies. Validate SAS programs, macros, datasets, and TFL output generated by other Programmers. Develop or assist in the development of departmental processes and procedures. Other duties as assigned. How You'll Get There: Experience working in Pharmaceutical/ Biotechnology/CRO industry as a Statistical Programmer is required (>= 3 years with MS degree; >=5 years with BS degree). High proficiency in SAS programming and Macro development Experience working with CDISC SDTM and ADaM compliant data sets Experience with regulatory submissions and creating Define.XML. Knowledge of statistics and the drug development process In-depth knowledge of FDA/ICH guidelines and industry/technology standard practices Knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs Capable of critical thinking and independently identifying issues in existing programs Solid verbal and written communication skills Bachelor's /Master's Degree in Statistics, Mathematics, Computer Science, or other related discipline is required; Master's degree is preferred

Contact: Neisha Camacho/Terra Parsons - ************************* No 3rd party candidates Senior Statistical Programmer to support programming activities within CNS in support of clinical trials and regulatory submissions. In this role, you will transform raw clinical data into analysis ready datasets, generate high-quality TLFs, and contribute to the continuous improvement of analysis workflows and programming processes. Key Responsibilities: Provide statistical programming support to generate SDTM and ADaM data sets, tables, listings, and figures for individual studies as well as ISS/ISE analyses. Provide programming support to internal teams including identifying, reporting, and resolving raw data issues Participate in the review of statistical analysis plans, table specification, develop specification for SDTM and ADaM data sets. Participate in study team meetings and address issues that may affect statistical programming. Support and participate in the preparation of clinical study reports, regulatory submissions, and annual DSUR and safety reports. Perform ad hoc analyses and data validation. Develop and maintain necessary programming macros or tools to effectively support all programming needs Develop and contribute to internal teams SOPs and working documents related to EDC studies, FDA requests, independent validation, and general statistical programming processes. Qualifications Bachelor's or Master's degree in biostatistics, computer science, or related fields 8 years in statistical programming within the pharmaceutical, biotechnology, or CRO industry, including regulatory submissions within CNS is preferred. Advanced SAS programming; CDISC standards expertise; knowledge of additional programming languages (R, Python) is a plus. Strong Macro and tool development and validation Experience in BLA, NDA/sNDA submissions. Proficiency in additional programming languages such as R or Python, along with experience using SAS/Graph and statistical packages, is preferred. Strong communication skills and the ability to collaborate within cross-functional teams to manage priorities and meet deadlines are essential.

Job DescriptionWe need following information when you apply to Ecclesiastes requirements. 1) Resume 2) Passport 3) Work Authorization As a Senior IT Applications Programmer, you will play a key role in designing, developing, and maintaining BizTalk integrations, ensuring seamless application support across multiple platforms. You will collaborate with various teams, including application programmers, QA analysts, and business partners, to deliver high-impact software solutions using methodologies such as Waterfall, Scrum, DevOps, and continuous delivery. Key Responsibilities: Design and develop BizTalk integrations supporting multiple applications. Analyze and resolve technical issues while proactively identifying improvements for resiliency and cost reduction. Support multiple Scrum delivery and waterfall project teams throughout the application lifecycle. Collaborate daily with application programmers, system analysts, QA teams, and business stakeholders. Required Skills & Qualifications: Proficiency in MS SQL Server, XML, XSLT, Visual Studio, and C# .NET. Experience developing and maintaining automated applications, primarily in BizTalk. Strong understanding of BizTalk architecture, core components, pub/sub architecture, and content-based routing. Familiarity with the Microsoft technology stack (Windows Server, Visual Studio, TFS, ADO pipelines). Excellent communication, organizational, and leadership skills. Ability to manage multiple projects in a fast-paced environment with tight deadlines. Proven ability to work effectively in a team-oriented and collaborative environment. Preferred Skills: Experience in Property & Casualty Insurance and/or Duck Creek. Familiarity with SoapUI, Postman, and API testing. Knowledge of Agile/SCRUM and DevOps methodologies. Once the profile has been shortlisted, we will set up the interview. This is a remote position.