Clinical Statistical Programmer Jobs Near Me

For immediate consideration, please connect with me on LinkedIn at ************************************** and then email your resume, work authorization status, current location, availability, and compensation expectations directly to ***************************** - make sure to include the exact job title and job location in your email message. To be considered for an interview, please make sure your application is full in line with the job specs as found below. Lead Data Scientist : - Lead various analytical projects for credit card decision science initiatives - Supervise junior analysts - Create data-driven presentations for product team collaboration - Develop and implement consumer lending strategies - Design and execute machine learning models for credit decisioning - Analyze large-scale credit card portfolio performance Required Qualifications (Skills, Experience, Education, Certifications) : - Master's degree in Statistics, Mathematics, Computer Science, or related quantitative field - Experience in consumer lending data analytics, preferably with a major financial institution - Experience with Python / PySpark for large-scale data analysis - Experience with data visualization tools, particularly Tableau - Experience with statistical analysis and machine learning model development - Knowledge of credit risk assessment and decision science methodologies For immediate consideration, please connect with me on LinkedIn at ************************************** and then email your resume, work authorization status, current location, availability, and compensation expectations directly to ***************************** - make sure to include the exact job title and job location in your email message. . Remote working/work at home options are available for this role.

Gaming & Gambling Industry Fully Remote - US (East Coast Hours) $140,000-$170,000 I am partnered with a global leader in online gaming innovation who is actively seeking a Data Scientist to join their growing Advanced Analytics team. If you thrive in a dynamic, fast-paced environment and are passionate about predictive modeling and customer behavior, this may be your role! The Role: Data Scientist As a Data Scientist, you will play a critical role in understanding player behavior across a vast user base of 35M+ players. You'll develop models to predict churn, optimize customer acquisition, and drive retention strategies that enhance loyalty and engagement. Your Skills & Experience: 2-3 years of experience in predictive analytics or data science. Hands-on expertise in churn prediction, LTV analysis, recommendation systems, and decision trees. Proficiency in Python (or R), with experience in Google Cloud Platform (Vertex AI preferred). Strong understanding of customer acquisition, retention, and loyalty analytics. Thrives in an agile, startup-like environment with a collaborative mindset. Bachelor's degree in math, statistics, or a related field. Benefits: Data Scientist Competitive base salary: $140K-$170K. Fully remote opportunity How to Apply? Please register your interest by sending your resume to Marina Mason. Keywords: Python, R, Churn Prediction, Recommendation Systems, Customer Acquisition, Customer Retention, Customer Loyalty, LTV, AB Testing, Predictive Modeling, Data Science, and Analytics.

Akkodis is recruiting for a Data Scientist for an aerospace manufacturer in the Evendale, OH area. This is an remote position with a pay range of $45 hour to $65 hour. Bachelor's degree on software, mechanical or mechatronics engineering. • 5+ years of experience including implementations and customer facing roles. • Data analysis tools such as R and Python. • Proficient knowledge of database applications such as SQL. • Excellent communication skills. • 5+ years of experience with Aerospace industry. • Fuel Efficiency knowledge is a Plus. Configuration of data visualization dashboards such as Tableau or PowerBI. If interested, forward resume to ***********************************

Before applying for this role, please read the following information about this opportunity found below. A/V Programmer Remote MUST: Experienced A/V Programmer 5+ years experience working in the AV/VTC industry in an applicable role. Must have experience as a programmer/Engineer Experience with Crestron program creation development, implementation of small to large-scale AV systems which include: video teleconferencing, audio teleconferencing, analog/digital video switching systems, sound systems, lighting, and displays. Experience design specifications, configuring and fine-tuning AV equipment Ability to work, think, determine, then establish priority of urgency quickly and accurately with little oversite to meet deadlines in an organized manner. Working knowledge of a wide range of audio, video, networking equipment and software including, but not limited to Biamp, Crestron, Extron, AMX, QSC, and Cisco. Ability to read and work from AV and general construction drawings. Competence in system configuration, software installation and hardware installation of common AV equipment in a production type environment. Understanding of low voltage electrical installation practices and concepts. Ability to pass background checks and work in secure government facilities. Must have a certification in one of the following: Biamp, Crestron, Extron, AMX Bachelors preferred DUTIES: Under the general direction, and supervision of the Director of Operations and Integration of the Unified Communications Solutions team or an assignee, the A/V Programmer will be the gate keeper of quality between the staging area and install site. Responsibilities will include interpreting design specifications, configuring and fine-tuning AV equipment such as projectors, displays, audio systems, and control interfaces. Proficiency in collaborating with project teams, including programmers and project managers, is essential. A keen attention to detail, you will meticulously document system configurations and provide timely solutions to challenges that may arise during the commissioning process. Will play an essential part in the success of every project. Properly checking equipment in and out of the warehouse. Un-boxing and re-boxing equipment for testing and configuration. Loading firmware, code, DSP files, and other hardware configurations. Documenting all required hardware information and settings. Fully setting up AV systems, testing, troubleshooting, updating, and re-testing systems until they operate at peak performance meeting the stated customer requirements. Trouble shooting issues and working with the proper vendor and/ or internal resources to determine root causes. Processing vendor related RMAs. Backing up final code versions and system documentation's. Communicate project status and lessons learned to internal stake holders. Assist with adding and documenting consumables to projects so installation teams have a complete, executable equipment package when they arrive onsite. The ability to act on supervisor instructions. Assist the Staging Area Rack Fabricator with maintaining the staging areas cleanliness, organization, and consumables stock. *Quadrant, Inc. is an equal opportunity and affirmative action employer. Quadrant is committed to administering all employment and personnel actions on the basis of merit and free of discrimination based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or status as an individual with a disability. Consistent with this commitment, we are dedicated to the employment and advancement of qualified minorities, women, individuals with disabilities, protected veterans, persons of all ethnic backgrounds and religions according to their abilities.

Role Overview & Key Functions: The Principal Statistical Programmer will play a critical role in advancing clinical trial research and regulatory submissions. This position offers the opportunity to lead statistical programming efforts, including developing and validating datasets, creating files for regulatory submissions, and collaborating with cross-functional teams to ensure compliance with CDISC data standards. If you're passionate about driving excellence in statistical programming and contributing to life-changing clinical development programs, this role provides the perfect platform to make a meaningful impact. Reporting to our Senior Director, Statistical Programming you will positively impact patients' when you: Reviews and understands study documents, including the Protocol, electronic case Report Forms (eCRFs) and Statistical Analysis Plans (SAPs). Reviews and understands raw eDTC database structure. Participates in Statistical Analysis Plan (SAP) development and review. Participates in TLF shells development and review. Driver of Statistical Programming projects. Major contributor to the development of Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM) dataset specifications. Leads projects in close partnership with Biostatisticians. Develops global standard macros to improve the efficiency of the Statistical Programming Group. Creates define.xml for regulatory submissions. Uses CDISC validation software to ensure SDTM and ADaM datasets comply with regulations. Oversees vendors for outsourced statistical programming work. Mentors less experienced programmers. Represents the Statistical Programming Group at cross functional team meetings. Candidate Profile & Requirements: BS in Mathematics, Biostats/Statistics, Computer Science/Data Science or related field Required. MS/PhD in Biostatistics/Statistics/CS/Data Science, Public Health or related field preferred. 8 - 12 years of Phase 1-Phase 3 clinical trials conducted in biotech/pharmaceutical/CRO environment experience required. Experience in Oncology therapeutic area a plus. Expertise in SAS required. R or other statistical software a plus. Experience in support of electronic submissions in electronic Common Technical Document (eCTD) format a plus. Experience with Clinical Data Standards Consortium (CDISC) data standards SDTM and ADaM preferred. Experience supporting an Integrated Summary of Safety (ISS) or Integrated Summary of Efficacy (ISE) a plus. Our Value Proposition: At Karyopharm, we live and demonstrate our ICARE values every day! If you want to do something that matters, this work matters. Patients drive our passion to pioneer novel cancer therapies. That's why we've built an environment centered around support, flexibility, and a shared mission. Creating and delivering medicine for cancer can only be done through focus, dedication, and heart. We hire exceptional people and trust each other to work in whatever way lets us, be us - whether that's onsite, from home, or anywhere in between. What do you get when you pair an extraordinary mission with a culture of flexibility and empowerment? We invite you to find out and join us on this incredible mission. Check out our Culture Video! What We Offer: In addition to our exciting, supportive, and intellectually challenging global workspaces(s), team members enjoy a comprehensive and generous benefits package (active on day one) that makes them more productive and contributes directly to the development of their professional skills. A culture of employee engagement, diversity, and inclusion Competitive salary, bonus, and generous equity offerings (RSU's at time of offer and annual awards) - we are partners in prosperity! Peace of mind through best in class medical (deducible paid by KPTI), dental, vision, disability, and life insurance, parental leave, a matching 401k program (immediate vesting), ESPP and tuition reimbursement. Wellness Program with a monthly stipend. Generous Flex Time Off program and Holidays - we encourage you to recharge and spend time with family and friends. Ample opportunities to learn and take on new responsibilities in a fast-paced, and patient focused company. (tuition reimbursement, management development & mentoring programs, and a variety of reward and recognition programs) Cell phone allowance In the U.S., the salary range for this position is $160,000 to $175,000 per year, which factors in various geographic regions. The base pay actually offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors

**Summary:** IQVIA is hiring a Principal Statistical Programmer to join a sponsor-dedicated, RWE biometrics team. Expect to work fully within the sponsor environment to progress with long-term study initiatives. Contribute to establishing processes and standards for RWE/RWD and establish yourself as a key resource in this area. Apply your skills in both SAS and R programming. **Job Expectations:** + Serves as statistical programming member and represents Biometrics on health outcomes and epidemiology studies. + Collaborates with the study statistician to design data structure and specifications for programming study deliverables including ADaM datasets, Tables, Listings and Figures. Contribute to leading the production and validation efforts for the outputs. + Ensure all programming activities comply with CDISC standards (SDTM and ADaM) and regulatory guidelines. + Leverages administrative claims, electronic medical records, or other real-world data to complete appropriate study tasks. + Identifies innovation opportunities for the use of real-world data (RWD). **Qualifications:** + Bachelors degree in Statistics, Mathematics, Computer Sciences, Pharmacology, Biology or similar. + Ideal candidates with have 7+ years of experience working within a pharmaceutical or clinical research setting. + Must have excellent knowledge of CDISC standards. + Strong SAS programming skills when applying to clinical trial data. + Moderate level skills in R programming with organizational and data analysis purposes. + Experienced with handling real-world data (RWD) with advanced content knowledge. + Experienced with clinical trial data and extremely hands-on in data manipulations, analysis, and reporting of analysis results. + Excellent organizational skills and proven ability to effectively lead multiple projects to successful completion. + Ability to effectively interpret and communicate research results to internal and external audiences. **Location:** Work-from-home. Candidates located in the U.S. or Canada can be considered. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at ********************** We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. **********************/eoe IQVIA's ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status. **********************/covid-19-vaccine-status The potential base pay range for this role, when annualized, is $106,200.00 - $177,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare - and human health - forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes. To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $96,000 - $162,800 At Lilly, we serve an extraordinary purpose. We make a difference for people around the global by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism. The Clinical Study Build Programmer is responsible for programming and testing clinical trial data collection databases, including the mapping, testing and normalization of data into a clinical data warehouse. This requires an in depth understanding of data technology, data flow, data standards, database programming, normalization and testing. This role will collaborate with Data and Analytics colleagues such as the Clinical Data Associate, Clinical Data Manager and other key partners to deliver standardized data collection methods and innovative validation solutions for use in global clinical trials. **Responsibilities:** This is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position. **Portfolio Delivery:** + Program and test data collection systems and associated data repository mappings for a trial or set of trials within a program using data standards library components + Ensure data collection systems and data warehouse mappings are delivered accurately, efficiently and in alignment with study objectives + Provide insights into study level deliverables (i.e. Data Management Plan, Project Plan, database, and observed datasets) + Support submission, inspection and regulatory response activities + Lead cross Business Unit/Therapeutic Area projects or programs with high complexity + Opportunity to develop and tests new ideas and/or applies innovative solutions that add new value to the portfolio **Project Management:** + Increase speed, accuracy, and consistency in the development of systems solutions + Enable metrics reporting of study development timelines and pre and postproduction changes to database + Partner to deliver study database per business need and before first patient visit + Follow and influence data standard decisions and strategies for a study and/or program + Apply therapeutic knowledge and possess a deep understanding of the technology used to collect clinical trial data + Effectively apply knowledge of applicable internal, external and regulatory requirements/expectations (MQA, CSQ, MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to study build deliverables + Integrates multi-functional and/or external information and applies technical knowledge to data-driven decision making **Enterprise Leadership:** + Continually seek and implement means of improving processes to reduce study build cycle time, decrease work effort and enable the normalization of various sources of data into a common data repository in a way that allows for improved integration, consumption and downstream analysis + Represent Data and Analytics processes in multi-functional initiatives + Actively engage in shared learning across the organization + Work to Increase re-usability of forms and edits by improving the initial design + Work to reduce postproduction changes change control process + Anticipate and resolve key technical, operational or business problems that impact the Data and Analytics organization + Interacts with regulators, business partners and outside stakeholders on business issues + Thinks with end to end in mind consistently managing risk to minimize impact on delivery + Builds a diverse multi-functional and internal/external network to understand how different disciplines and approaches contribute to research and development + Focuses on defining database solutions and timelines in support of advancing the portfolio **Basic Qualifications:** + Master's degree with 5 years of experience in database programming or system validation experience in the clinical, pharmaceutical, biotech, CRO or regulatory agency sectors(or Bachelor's degree with 7 or more years of experience) + Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position **Additional Preferences:** + Knowledge of regulatory guidelines such as GCP, 21 CFR Part 11 etc. + Knowledge of industry standard clinical technologies including CTMS, EDC (Veeva CDMS preferred, Rave, InForm), eCOA, IxRS, Clinical Data Repositories, etc. + Knowledge of CDISC and CDASH standards/standard terminology + Ability to work independently as well as in a team environment. + Minimum 4 years' oncology experience preferred. + Project and Vendor management experience + Excellent time management skills and a proven ability to work on multiple projects at any given time in a fast-paced environment. + Demonstrated ability to stay abreast of trends and new information in the profession. + Quick learner to new trends in technology + Excellent leadership, communication (written and oral) and interpersonal skills + Demonstrated teamwork and collaboration in a professional setting **Experience with the following:** + Articulating the flow of data (structure and format) from patient to analysis and apply this knowledge to data solutions + Deciding the technology platform (system/database) for data acquisition and aggregation + Utilization of clinical/drug development knowledge and an ability to liaise effectively with study team members (i.e. Data Sciences, Statistics, PK, Operations, Medical) + Strong therapeutic/scientific knowledge in the field of research + Society of Clinical Data Management certification + Project management experience + Familiarity with clinical data tools and technologies + Understanding and experience in using data standards + Ability to balance multiple activities, prioritize and manage ambiguity + Demonstrated exemplary teamwork/interpersonal skills + Proven problem solving, attention to detail and result oriented behaviors in a fast-paced environment. **Other Information:** + Domestic and International travel may be required _Lilly currently anticipates that the base salary for this position could range from between $96,000 to $162,800 and will depend, in part, on the successful candidate's qualifications for the role, including education and experience. Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Of course, the compensation described above is subject to change and could be higher or lower than the range described above. Further, Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees._ _*To perform this job successfully, an individual must be able to perform the role and responsibilities satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions._ Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( ******************************************************* ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women's Network, Working and Living with Disabilities. Learn more about all of our groups. Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. \#WeAreLilly

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

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 (Greater Toronto Area), Ontario, Canada with additional sites in Bridgewater, New Jersey, USA, Taipei, Taiwan, and Shanghai (Pudong Zhangjiang New District), China. 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 **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 **************** 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. **Qualifications** **Skills** **Behaviors** **:** **Motivations** **:** **Education** **Experience** **Licenses & Certifications** Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c)

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 (Greater Toronto Area), Ontario, Canada with additional sites in Bridgewater, New Jersey, USA, Taipei, Taiwan, and Shanghai (Pudong Zhangjiang New District), China. 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 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 **************** 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.

Ionis Pharmaceuticals, Inc., is headquartered in Carlsbad, California, with offices in Boston, Massachusetts, and Dublin, Ireland. For more than 30 years, Ionis has been the leader in RNA-targeted therapy, pioneering new markets and changing standards of care with our novel antisense technology. Ionis currently has three marketed medicines and a premier late-stage pipeline highlighted by industry-leading cardiovascular and neurological franchises. Our scientific innovation began and continues with the knowledge that sick people depend on us, which fuels our vision to become the undisputed leader in genetic medicine, utilizing a multi-platform approach to discover, develop and deliver life-transforming therapies. As the first company to fully harness the power of RNA technology for human therapeutics, Ionis' platform continues to revolutionize drug discovery and transform lives for patients with unmet needs. We are building upon our innovative research and drug development excellence to provide greater value to patients, and we are well positioned financially to deliver on our strategic goals. Ionis is a challenging, motivating and rewarding environment designed to foster innovation and scientific excellence. Our success is a direct result of our outstanding employees. We are interested in bringing together a diverse group of individuals with different skill sets and perspectives into this creative environment to be part of a productive and inclusive team. While acknowledging people are actively engaged in hybrid/remote work, we continue to invest time, money, and energy into making our workplace locations a place where our culture and employees can thrive. We believe engaging on a day-to-day basis, in person, builds solid and lasting relationships, and contributes positively to our culture and innovation. From the heart of our stunning Carlsbad campus, we aim to provide a central connection point for all our employees. These facilities give us the opportunity to connect cross-functionally, collaborate and to build on the success of our business as we continue to grow. Join us and experience our unique culture while you develop and expand your career. CLINICAL PROGRAMMER I - CLINICAL DATA SCIENCE SUMMARY: As a Clinical Data Science (CDS) Clinical Programmer I, you will be responsible for utilizing the R and/or Python programming language to create both textual and graphical data displays that facilitate data cleaning and data review. You will work under the direction of a more experienced programmer to expand your programming skill set as you program scripts to create data manager/analyst requested data displays. This role requires a detail-oriented person that enjoys problem solving, has some previous programming experience in any language, and enjoys learning new programming techniques. RESPONSIBILITIES: * Utilize R/Python to restructure and present raw clinical trial data in ways that streamline the data cleaning and data review processes * Work under the direction of an experienced programmer to learn/extend their R/Python skill set * Create data visualizations to present clinical data effectively * Write and maintain R/Python programs that include comments describing the steps performed throughout the R/Python program * Adhere to company and departmental policies and procedures COMPETENCIES IDENTIFIED FOR SUCCESS: * Solid analytical and proactive problem-solving skills * A team player with strong interpersonal skills * Effective written and verbal communication skills * Outstanding organizational skills with the ability to multitask and prioritize REQUIREMENTS: * Bachelor's or Master's degree * Some experience with a programming language Please visit our website, ******************* for more information about Ionis and to apply for this position; reference requisition # IONIS003436 Ionis offers an excellent benefits package! Follow this link for more details: Ionis Benefits Full Benefits Link: https://*******************/careers/working-at-ionis/#:~:text=our%20employee%20spotlight-,Benefits,-Employees%20are%20rewarded The pay scale for this position is $67,466 to $89,117 NO PHONE CALLS PLEASE. PRINCIPALS ONLY. Ionis Pharmaceuticals, Inc. and all its subsidiaries are proud to be EEO employers.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $96,000 - $162,800 At Lilly, we serve an extraordinary purpose. We make a difference for people around the global by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism. The Clinical Study Build Programmer is responsible for programming and testing clinical trial data collection databases, including the mapping, testing and normalization of data into a clinical data warehouse. This requires an in depth understanding of data technology, data flow, data standards, database programming, normalization and testing. This role will collaborate with Data and Analytics colleagues such as the Clinical Data Associate, Clinical Data Manager and other key partners to deliver standardized data collection methods and innovative validation solutions for use in global clinical trials. Responsibilities: This is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position. Portfolio Delivery: Program and test data collection systems and associated data repository mappings for a trial or set of trials within a program using data standards library components Ensure data collection systems and data warehouse mappings are delivered accurately, efficiently and in alignment with study objectives Provide insights into study level deliverables (i.e. Data Management Plan, Project Plan, database, and observed datasets) Support submission, inspection and regulatory response activities Lead cross Business Unit/Therapeutic Area projects or programs with high complexity Opportunity to develop and tests new ideas and/or applies innovative solutions that add new value to the portfolio Project Management: Increase speed, accuracy, and consistency in the development of systems solutions Enable metrics reporting of study development timelines and pre and postproduction changes to database Partner to deliver study database per business need and before first patient visit Follow and influence data standard decisions and strategies for a study and/or program Apply therapeutic knowledge and possess a deep understanding of the technology used to collect clinical trial data Effectively apply knowledge of applicable internal, external and regulatory requirements/expectations (MQA, CSQ, MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to study build deliverables Integrates multi-functional and/or external information and applies technical knowledge to data-driven decision making Enterprise Leadership: Continually seek and implement means of improving processes to reduce study build cycle time, decrease work effort and enable the normalization of various sources of data into a common data repository in a way that allows for improved integration, consumption and downstream analysis Represent Data and Analytics processes in multi-functional initiatives Actively engage in shared learning across the organization Work to Increase re-usability of forms and edits by improving the initial design Work to reduce postproduction changes change control process Anticipate and resolve key technical, operational or business problems that impact the Data and Analytics organization Interacts with regulators, business partners and outside stakeholders on business issues Thinks with end to end in mind consistently managing risk to minimize impact on delivery Builds a diverse multi-functional and internal/external network to understand how different disciplines and approaches contribute to research and development Focuses on defining database solutions and timelines in support of advancing the portfolio Basic Qualifications: Master's degree with 5 years of experience in database programming or system validation experience in the clinical, pharmaceutical, biotech, CRO or regulatory agency sectors(or Bachelor's degree with 7 or more years of experience) Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position Additional Preferences: Knowledge of regulatory guidelines such as GCP, 21 CFR Part 11 etc. Knowledge of industry standard clinical technologies including CTMS, EDC (Veeva CDMS preferred, Rave, InForm), eCOA, IxRS, Clinical Data Repositories, etc. Knowledge of CDISC and CDASH standards/standard terminology Ability to work independently as well as in a team environment. Minimum 4 years' oncology experience preferred. Project and Vendor management experience Excellent time management skills and a proven ability to work on multiple projects at any given time in a fast-paced environment. Demonstrated ability to stay abreast of trends and new information in the profession. Quick learner to new trends in technology Excellent leadership, communication (written and oral) and interpersonal skills Demonstrated teamwork and collaboration in a professional setting Experience with the following: Articulating the flow of data (structure and format) from patient to analysis and apply this knowledge to data solutions Deciding the technology platform (system/database) for data acquisition and aggregation Utilization of clinical/drug development knowledge and an ability to liaise effectively with study team members (i.e. Data Sciences, Statistics, PK, Operations, Medical) Strong therapeutic/scientific knowledge in the field of research Society of Clinical Data Management certification Project management experience Familiarity with clinical data tools and technologies Understanding and experience in using data standards Ability to balance multiple activities, prioritize and manage ambiguity Demonstrated exemplary teamwork/interpersonal skills Proven problem solving, attention to detail and result oriented behaviors in a fast-paced environment. Other Information: Domestic and International travel may be required Lilly currently anticipates that the base salary for this position could range from between $96,000 to $162,800 and will depend, in part, on the successful candidate's qualifications for the role, including education and experience. Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Of course, the compensation described above is subject to change and could be higher or lower than the range described above. Further, Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. *To perform this job successfully, an individual must be able to perform the role and responsibilities satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women's Network, Working and Living with Disabilities. Learn more about all of our groups. Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

- Job Description **Statistical Programmer** Contract: New Jersey, New Jersey, US Salary: $70.00 Per Hour Job Status: Expired **This Job is no longer accepting applications** **About the Role:** * We are seeking an Outcomes Research Stats Analyst/ Statistical Programmer to join our team. * The successful candidate will report to the Director of Data Analytics OR of Medical Affairs Outcomes Research. * The role will focus on Women's Health, Established Brands, Biosimilars, and in-licensing opportunities. * The primary responsibility will be to conduct internal analysis for all internal projects and research programs, delivering insights and research projects. **Responsibilities**: * Conduct internal data analysis for observational studies related to developmental products and commercialized projects. * Communicate data insights to internal stakeholders and provide support for research projects going to congress and manuscript submission. * Develop protocols and Statistical Analysis Plan (SAP) based on study concepts, ensuring appropriate study design, sample size, and statistical methodologies. * Implement rigorous QC processes and programming templates to maintain data and analysis quality. **Education Qualification:** * Minimum Masters degree in Health Economics, Biostatistics, Health Services Research, Public Health, Epidemiology, Pharmacy Administration, or related discipline. * Advanced degree (PhD, DrPH, PharmD) is a plus. * Must have publications on resumes. **Required Skills:** * Minimum 3 years of SAS programming experience and 2 years of hands-on work with real-world studies using large claims/EMR databases in HEOR. * Strong programming skills in SAS/R programming and data analysis. * Extensive experience with US insurance claims databases, electronic medical records, and registry databases for health outcomes research. * Familiarity with medical and billing coding systems such as ICD-10, SNOMED, LOINC, NDC, HCPCS, CPT. * Experience with Ex-US healthcare databases is a plus. * Previous work in the pharma industry and therapeutic area expertise preferred. * Knowledge of claims or EMR databases for research purposes. * Notes: - 100% Remote role, candidates on the east coast preferred. **Privacy Overview** CookieDurationDescription

Purpose: Join our FSP team today! In this role you will plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements. Job Details: Position: - Principal Statistical Programmer Home Based Min 4+ years of CRO/Pharma Industry Therapeutic Areas: Oncology // Immunology // IDV // EDCP Key Skills: Must have expertise of R programming as well as SAS Base, and good knowledge of SAS graph and SAS Macros. Capable of implementing more advanced statistical procedures as per specifications provided by biostatistician. Must have excellent knowledge of CDISC standards (SDTM and ADaM) Thorough understanding of relational database components and theory. Excellent application development skills. Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results. Good understanding of ICH E6, ICH E3, ICH E8, ICH E9 and clinical research processes. Minimum of 4+ years of experience in Statistical Programming in pharmaceutical or medical devices industry Good verbal and written communication skills. Ability to work on multiple projects, plan, organize and prioritize activities. Required Knowledge, Skills and Abilities: Experience as technical team lead directly engaging clients and coordinating tasks within a programming team In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Knowledge of statistics, programming and/or clinical drug development process Advanced knowledge of R programming Base SAS, SAS/STAT, SAS Graph and SAS Macro Language Should have experience with SDTM Implementation and ADaM implementation according to CDISC Standards. Must have expertise in SAS/BASE, SAS/MACRO, SAS/STAT, SAS/GRAPH, SAS/ACCESS, SAS/ODS, SAS/SQL. Good organizational, interpersonal, leadership and communication skills Ability to independently manage multiple tasks and projects Ability to delegate work to other members of the SP team Excellent accuracy and attention to detail Ability to delegate work to other members of the SP team [SPM] Exhibits routine and occasionally complex problem-solving skills Ability to lead teams and projects and capable of managing at a group level Recognizes when negotiating skills are needed and seeks assistance. Ability to establish and maintain effective working relationships with co-workers, managers and clients. Responsibilities: Perform, plan co-ordinate and implement the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing and (ii) the programming of analysis datasets (derived datasets) and transfer files for internal and external clients and (iii) the programming quality control checks for the source data and report the data issues periodically.. Ability to interpret project level requirements and develop programming specifications, as appropriate, for complex studies. Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams and Statistical Programming department, for complex studies. Fulfil project responsibilities at the level of technical team lead for single complex studies or group of studies. Directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines. Estimate programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables. Use and promote the use of established standards, SOP and best practices. Provide training and mentoring to SP team members and Statistical Programming department staff. MINIMUM REQUIRED EDUCATION AND EXPERIENCE: Bachelor's degree from reputable university preferably in science/ mathematics related fields IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at ********************** We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. **********************/eoe IQVIA's ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status. **********************/covid-19-vaccine-status The potential base pay range for this role, when annualized, is $117,400.00 - $218,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Principal Data Scientist Data Intelligence **Principal Data Scientist** * Irving, Texas * Alpharetta, Georgia * Boston, Massachusetts * US: Irving, Texas * Alpharetta, Georgia * Boston, Massachusetts * Ashburn, Virginia * Temple Terrace, Florida * Basking Ridge, New Jersey Job ID: R-1058906 **When you join Verizon** **What you'll be doing...** The Artificial Intelligence & Data (AI&D) Organization is an exciting center of excellence supporting all of Verizon. Our team is a catalyst to Verizon's future in creating networks that move the world forward through the power of Artificial Intelligence & Data. You will be a strategic thinker joining a high-profile, high-visibility team that powers data science and strategic thinking for Verizon. You will be part of a team that builds tools, analyses, and insights that informs, quantifies, and enables the visualization of data to drive business decisions for all of Verizon's Networks. With your analytical, big data and AI/ML expertise, you will deliver business value through business intelligence and data science by driving insights to actions. One way you will accomplish this is by developing analytical views of data utilizing various BI and data science such as Tableau, Qlik, Looker, Python and other analytical toolsets. You will also connect various databases to stage data. The business insights and recommendations you provide will help to improve Verizon's performance across multiple key business metrics. * Analyzing large-scale and complex datasets (including 3rd party benchmarking data) to identify how network metrics correlate with each other and correlate to customer experience. * Analyzing strategic implications of major competitive initiatives through automated data collection of competitive events and product launches using publicly available data sources and third-party data. * Leading the creation of new automated competitive data pipelines including automated insights that drive improved data-driven decisions through studying best-in-class industry practices and colloboration with Verizon GenAI practice. * Engaging directly with data providers to ensure the data is accurately collected, measured and reported. * Performing ad-hoc analysis and developing reproducible analytical approaches to meet business requirements. * Performing exploratory and targeted data analyses using descriptive statistics and other methods. * Performing geospatial analyses and creating geospatial visualizations to respond to business requests. * Preparing executive level presentations to clearly articulate results of complex mathematical analysis through strategic storytelling. * Designing, developing, implementing, and overseeing high-end analytical/technology processes and solutions with a focus on leveraging advanced machine learning and artificial intelligence methods. * Automating and using the latest technology, such as NLP (natural language processing), GenAI, to analyze market data about our competitors to keep a pulse on impactful new products and network design, as well as integrate major macroeconomic, social, and political indicators into strategic planning. * Collaborating across multiple teams within the business including Network, Verizon Consumer Group, Verizon Business, data engineering and ML engineering. **What we're looking for...** With an eye towards improving performance and predictability, you like the science of analytics. Developing resolutions to complex problems, using your sharp judgment to develop methods, techniques, and evaluation criteria allows you to deliver solutions that make a huge impact. You're able to communicate technical information to non-technical audiences, and you take pride in your ability to share your considerable knowledge with your peers. You'll need to have: * Bachelor's degree or four or more years of work experience * Six or more years of relevant experience required, demonstrated through one or a combination of work and/or military experience or specialized training * Experience applying statistical ideas and methods to data sets to answer business problems * Experience with developing insights, presenting, and influencing strategic decisions using data * Experience in programming languages such as SQL and Python and visualization tools like Tableau Even better if you have one or more of the following: * Degree in business intelligence and analytics, computer science, or mathematics * Master's degree * Knowledge of basic wireless network and performance KPIs. * Self-starter who can quickly learn new products from scratch and identify their key differentiators * Experience with Data Warehousing or Teradata SQL * Knowledge of distributive computing tools, like Hive or Spark * Experience with SiteCatalyst/Clickstream * Experience with programming languages, like Java, Python, or Scala If Verizon and this role sound like a fit for you, we encourage you to apply even if you don't meet every “even better” qualification listed above. **Where you'll be working** In this hybrid role, you'll have a defined work location that includes work from home and a minimum eight assigned office days per month that will be set by your manager.**Scheduled Weekly Hours** 40**Equal Employment Opportunity** We're proud to be an equal opportunity employer - and celebrate our employees' differences, including race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, and Veteran status. At Verizon, we know that diversity makes us stronger. We are committed to a collaborative, inclusive environment that encourages authenticity and fosters a sense of belonging. We strive for everyone to feel valued, connected, and empowered to reach their potential and contribute their best. Check out page to learn more. **Privacy Preference Center** ** Manage Consent Preferences** Always Active **Targeting Cookie**

Outlier helps the world's most innovative companies improve their AI models by providing human feedback. Are you an experienced Math Expert who would like to lend your expertise to train AI models? **Please note this job requires fluency in German** About the opportunity: Outlier is looking for talented Math Experts to help train generative artificial intelligence models This freelance opportunity is remote and hours are flexible, so you can work whenever is best for you You may contribute your expertise by… Assessing the factuality and relevance of domain-specific text produced by AI models Crafting and answering questions related to Math Evaluating and ranking domain-specific responses generated by AI models Examples of desirable expertise: A bachelor's or higher degree in Math or a related subject Experience working as a Math professional Ability to write clearly about concepts related to Math in fluent English and German Payment: Currently, pay rates for core project work by Math experts in Austria range from $30 to $50 USD per hour Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project. PLEASE NOTE: We collect, retain and use personal data for our professional business purposes, including notifying you of opportunities that may be of interest and sharing with our affiliates. We limit the personal data we collect to that which we believe is appropriate and necessary to manage applicants' needs, provide our services, and comply with applicable laws. Any information we collect in connection with your application will be treated in accordance with the Outlier Privacy Policy and our internal policies and programs designed to protect personal data. This is a 1099 contract opportunity on the Outlier.ai platform. Because this is a freelance opportunity, we do not offer internships, sponsorship, or employment. You must be authorized to work in your country of residence. If you are an international student, you may be able to sign up for Outlier if you are on a visa. You should contact your tax and/or immigration advisor with specific questions regarding your circumstances.

** King Show Games, Inc.** ** Mathematician** Minnetonka, MN 55305 King Show Games, Inc., a video game development company, is currently interviewing qualified applicants interested in pursuing a career in video game development. We are looking for people who are innovative, talented, creative, and passionate about the gaming industry. If you're a self-motivated team player who is able to multi-task and can handle the following responsibilities, we look forward to hearing from you! **Job Summary**Our Mathematicians are responsible for designing and proofing math models for gaming products and working closely with the game development artists, engineers, and sound designers. The Mathematician should be a dynamic contributor to ensuring a fun, consistent, and competitive product that enhances player enjoyment. ****Responsibilities**** * Working with the game designer to develop feasible math models with the players' needs in mind. * Providing formal analysis and proofs of gaming math models. * Creating and maintaining/enforcing a clear, clean directory structure for all math assets as well as maintaining all documents relating to the math. * Managing the ongoing development of the math documentation to ensure that it remains accurate and up-to-date. * Ensuring a fun, consistent, and competitive product within the scope of the project. * Maximizing the use of existing technology. * Is an active participant/contributor in the game design and invention process. * Working closely with the Game Development team of artists, sound designers and game designers to design, develop, modify, review, test and document software in a real-time environment. * Working with the game programmer to ensure proper implementation of the math model. * Playing the game frequently to review the math implementation and providing team with constructive feedback as necessary. * Contributing to daily game design, implementation, and tuning efforts. * Delivering quality work as scheduled in accordance with the game design and product requirements. * Conforming to the math standards. ****Qualifications Required**** * Bachelor's Degree in mathematics, statistics or related. * Keen knowledge of applied mathematics, probability and statistics. * Ability to create spreadsheets and software simulations to verify math models. * Ability to interface and communicate with other members of the game development staff. * Ability to bring projects to completion with minimal supervision. * Good written and verbal communication skills and a high level of interpersonal skills. * Must be a self-motivated team player with the ability to work in a customer-oriented, very fast-paced, demanding and deadline-oriented environment. * Must be able to meet or exceed set project milestones and deadlines (self-motivated), which will entail extra work time as needed (work hours beyond a normal work week). * Skills and ability to identify problems, analyze the situation and make appropriate recommendations and decisions to achieve team goals. * Strong Excel skills are required. * Additional Software: Word, Outlook, Visual Studio.net Professional and ability to learn new applications. * Game development experience a plus. * Data mining experience a plus. * Basic familiarity with VBA and/or C++ a plus. Please include a cover letter along with your resume when you apply. This job description should not be interpreted as all-inclusive; it is intended to identify major responsibilities and requirements of the job. The incumbent may be requested to perform other job-related tasks and responsibilities other than those stated above. **About King Show Games**Founded in 1998, King Show Games is a Minnesota based company providing entertaining video games that are played around the world. Our growing company consists of talented artists, engineers, mathematicians and producers that have created over 200 games. Our Company Beliefs consist of four principles: **THINK BIG** - Think outside the box; strive to be successful. **BE FRANK** - Be open and sincere in your dealings with others; be forthright. **FIGHT HARD** - Believe in your ideas; speak up for your convictions. After the call, **MOVE AS A TEAM**! King Show Games offers competitive salaries and remote work options as well as a full range of comprehensive benefits including a bonus plan, medical, dental, life and long-term disability insurance, as well as a matching 401k. King Show Games embraces diversity and inclusion as an equal opportunity employer. We pride ourselves on creating an environment that is built on integrity, openness, involvement, fairness, respect and courtesy. \_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_ Recruiters, please don't contact King Show Games. Applicants, no phone calls or direct messages about this job please! Please do not contact King Show Games about other services, products or commercial interests.

Our company is currently seeking a Quantitative Analytics Senior responsible for the creation, development, and execution of analytic models Qualifications •PhD in Economics, Statistics, or a directly related quantitative field or MS with at least three years of related post-graduate work experience. •Strong programming skills in statistical programming languages such SAS, R, and Matlab. •Experience in using complex statistical models such as Generalized Additive Models, transition models, and logistic regression. Preferred Skills •Exceptional quantitative, empirical analysis, and research skills. •Programming experience with SAS, R and Matlab. •Experience with competing-risk hazard models and transition-based models. •Good communication, interpersonal, and leadership skills. •Experience working with large data sets. •Good communication, interpersonal, and leadership skills. Closing Statement Today, our company makes home possible for one in four home borrowers and is one of the largest sources of financing for multifamily housing. Join our smart, creative and dedicated team and you'll do important work for the housing finance system and make a difference in the lives of others. Our company is an equal opportunity and top diversity employer. EOE, M/F/D/V. Division Enterprise Risk Mgmt 2+ to 5 years experience Minimum Education - Doctorate Degree Additional Information All your information will be kept confidential according to EEO guidelines.

Introduction At IBM, we're revolutionizing our approach to technology sales. Our Client Engineering teams are champions of co-creating solutions in real-time to solve complex business challenges. As an AI Engineer within our Client Engineering team, you'll harness your unique skills and perspectives to engage in the development and deployment of AI systems using our watsonx platform, creating 4-to-6-week pilots for clients, and contributing to IBM's story of growth and innovation. In this role, you'll partner with technical leaders across IBM and drive client engagements with a curiosity that sparks innovation and learning. Your contributions will form a cornerstone in our sales strategy, facilitating rapid client delivery and product innovation. At IBM the possibilities are endless. We offer extensive onboarding and ongoing development, fostering an environment where you can thrive and shape your own career trajectory. Surrounded by a supportive team, you'll be integral in creating user-centric, compelling pilots that lead clients to continually invest in IBM's people, products, and services. Your Role and Responsibilities WASHINGTON, DC METRO An AI Engineer at IBM is not just a job title - it's a mindset. You'll leverage the watsonx platform to co-create AI value with clients, focusing on technology patterns to enhance repeatability and delight clients. Success is our passion, and your accomplishments will reflect this, driving your career forward, propelling your team to success, and helping our clients to thrive. Your primary responsibilities will include: * Proof of Concept (POC) Development: Develop POCs to validate and highlight the feasibility and effectiveness of the proposed AI solutions. Collaborate with development teams to implement and iterate on POCs, ensuring alignment with customer requirements and expectations. * Collaboration and Project Management: Collaborate with cross-functional teams, including data scientists, software engineers, and project managers, to ensure smooth execution and successful delivery of AI solutions. Effectively communicate project progress, risks, and dependencies to stakeholders. * Solution Implementation and Deployment: Oversee the implementation and deployment of AI solutions, working closely with development teams to ensure adherence to best practices, quality standards, and performance requirements. Provide technical guidance and support during the implementation phase. * Solution Optimization and Performance: Continuously monitor and optimize the performance of AI solutions, including foundation models and large language models. Identify opportunities to enhance efficiency, accuracy, and speed through fine-tuning, algorithmic improvements, or infrastructure optimization. * Customer Engagement and Support: Act as a technical point of contact for customers, addressing their questions, concerns, and feedback. Provide technical support during the solution deployment phase and offer guidance on AI-related best practices and use cases. * Documentation and Knowledge Sharing: Document solution architectures, design decisions, implementation details, and lessons learned. Create technical documentation, white papers, and best practice guides. Contribute to internal knowledge sharing initiatives and mentor new team members. * Industry Trends and Innovation: Stay up to date with the latest trends and advancements in AI, foundation models, and large language models. Evaluate emerging technologies, tools, and frameworks to assess their potential impact on solution design and implementation. FedSales24 Required Technical and Professional Expertise * Technical Skills: Strong programming skills, with proficiency in Python and experience with AI frameworks such as TensorFlow, PyTorch, Keras or Hugging Face. Understanding in the usage of libraries such as SciKit Learn, Pandas, Matplotlib, etc. Familiarity with cloud platforms (e.g. Kubernetes, AWS, Azure, GCP) and related services is a plus. * Technical Eminence: Proven experience as a technology thought leader, both internally and with clients * Soft Skills: Excellent interpersonal and communication skills. Engage with stakeholders for analysis and implementation. Commitment to continuous learning and staying updated with advancements in the field of AI. * Growth mindset: Demonstrate a growth mindset to understand clients' business processes and challenges. Preferred Technical and Professional Expertise * Experience: Proven experience in designing and delivering AI solutions, with a focus on foundation models, large language models, exposure to open source, or similar technologies. Experience in natural language processing (NLP) and text analytics is highly desirable. Understanding of machine learning and deep learning algorithms. *