Principal Statistical Programmer, Biometrics - Remote Agios PharmaceuticalsPrincipal Statistical Programmer, Biometrics - RemoteBoston, MARemote$131,035–$196,553 / yearThe current base salary range for this Senior Manager position is expected to be between $131,035 and $196,553 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators. Our team’s proven track record of executional excellence, combined with our depth of expertise and dedication, enables us to develop innovative medicines that reflect the priorities of rare disease communities.
SAS Programmer ClinPharma Clinical Research LLCSAS ProgrammerBoston, MA$80,000–$100,000 / yearInternFull timeThis role collaborates closely with researchers across the health system, providing comprehensive support throughout all stages of the research process—from proposal development to data analysis and interpretation. Core members offer expertise in: • Refining research questions and hypotheses.
Principal Statistical Programmer, Biometrics Agios Pharmaceuticals IncPrincipal Statistical Programmer, BiometricsCambridge, MA$131,035–$196,553 / yearThe current base salary range for this Senior Manager position is expected to be between $131,035 and $196,553 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators. Our team's proven track record of executional excellence, combined with our depth of expertise and dedication, enables us to develop innovative medicines that reflect the priorities of rare disease communities.
Lead Statistical Programmer Katalyst Healthcares & Life SciencesLead Statistical ProgrammerBoston, MAProvide leadership, project specific training, stakeholder management, external sponsor support, resource management, and project management for the required programming tasks supporting clinical trial activities. Create statistical analysis outputs to be used in support of final reports, abstracts, posters, Manu scripts, and other clinical publications; support systems to produce electronic regulatory submissions.
Lead statistical Programmer Katalyst Healthcares & Life SciencesLead statistical ProgrammerBoston, MAThe position involves hands-on technical leadership and requires comprehensive and detailed knowledge of statistical programming languages and software, filing support, clinical trial databases, and the drug development process. The role oversees external CRO partners to ensure high-quality, timely, and compliant delivery of analysis datasets, tables, listings, and figures that support clinical development and regulatory submissions.
Lead Statistical Programmer Karwell TechnologiesLead Statistical ProgrammerBoston, MAProvide leadership, project specific training, stakeholder management, external sponsor support, resource management, and project management for the required programming tasks supporting clinical trial activities. Create statistical analysis outputs to be used in support of final reports, abstracts, posters, Manu scripts, and other clinical publications; support systems to produce electronic regulatory submissions.
Lead statistical Programmer Karwell TechnologiesLead statistical ProgrammerBoston, MAThe position involves hands-on technical leadership and requires comprehensive and detailed knowledge of statistical programming languages and software, filing support, clinical trial databases, and the drug development process. The role oversees external CRO partners to ensure high-quality, timely, and compliant delivery of analysis datasets, tables, listings, and figures that support clinical development and regulatory submissions.
Statistical Programmer II LivaNova PlcStatistical Programmer IIBoston, MA$90,000–$100,000 / yearThe statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and therapies, as well as to generate evidence for marketed devices. Accountable for clinical statistical programming deliverables and for ensuring excellence in programming activities in terms of quality and timelines for clinical trials under the responsibility of Statistics & Data Management.
Associate Director, Statistical Programming Amylyx Pharmaceuticals IncAssociate Director, Statistical ProgrammingCambridge, MARemote$188,000–$211,000 / yearDevelop and execute statistical analysis and reporting deliverables (tables, figures and listings (TFLs)) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements. Ability to work on a multidisciplinary team that may include Biostatistics, Medical Directors, Data Management, Medical Writing, Pharmacovigilance, Clinical Operations, Medical Affairs, etc.
Associate Director, Statistical Programming Verastem IncAssociate Director, Statistical ProgrammingNeedham, MA$165,000–$190,000 / yearRequirements: Requirements include a Bachelor's or equivalent in Regulatory Affairs, Statistics, Computer Science or related field plus nine years of work experience in the job offered or related fields of clinical data and statistical programming in pharmaceutical or biotech industries; or in the alternative, a Master's degree or equivalent in Regulatory Affairs, Statistics, Computer Science or related field plus seven years of work experience in the job offered or related fields of clinical data and statistical programming in pharmaceutical or biotech industries. Applicants must have unrestricted authorization to work in the United States.
Director, Statistical Programming Seaport TherapeuticsDirector, Statistical ProgrammingBoston, MassachusettsLonger term, this leader will establish processes and SOPs, recruit and develop a high-performing team, and serve as a key member of the Biometrics leadership team driving continuous improvement. Lead the Statistical Programming function for Seaport Therapeutics; serve as programming representative on study and program teams and within the Biometrics leadership group.
Intern Statistical Programming Alnylam Pharmaceuticals IncIntern Statistical ProgrammingCambridge, MA$25–$35 / hour3. Tool Development and Workflow Optimization Build skills in developing proof-of-concept tools, automating routine tasks, and enhancing workflow efficiency, while documenting processes, testing solutions, and supporting adoption within a professional statistical programming environment. Overview The AI & Automation Intern will support the Statistical Programming department in exploring and implementing innovative artificial intelligence (AI) and machine learning (ML) solutions to enhance workflow efficiency, reduce manual effort, and streamline programming processes.
NewSenior Programmer (Clinical Study - 3) CSL PlasmaSenior Programmer (Clinical Study - 3)Waltham, MassachusettsWe use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas.
NewDirector, Statistical Programming Kura OncologyDirector, Statistical ProgrammingBoston, MA$234,644–$263,000 / yearMS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field with a minimum of 10-12 years of programming experience in the pharmaceutical industry, or BS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field with 12+ years of programming experience in the pharmaceutical industry. Kura developed and is commercializing KOMZIFTI® (ziftomenib), the FDA-approved once-daily, oral menin inhibitor for the treatment of adults with relapsed or refractory NPM1-mutated acute myeloid leukemia, and continues to pioneer advancements in menin inhibition and farnesyl transferase inhibition.
Director, Statistical Programming AstraZeneca PlcDirector, Statistical ProgrammingWaltham, MA$168,830.40–$253,245.60 / yearYou will also be part of the larger programming leadership team within oncology programming, and responsible for various activities beyond clinical trials, such as proving strategic or SME contributions on cross-functional teams to deliver continuous improvement, innovation, and automation solutions. We are now offering an exciting opportunity for a dedicated and highly motivated individual to join us in the role as Statistical Programming Director, providing strategic programming leadership and line management within Onc Biometrics and collaborating with global product development teams.
Statistical Programming Associate Director Sumitomo Pharma America Holdings Inc (Inactive)Statistical Programming Associate DirectorMarlborough, MA$168,000–$210,000 / yearResponsible for planning and tracking statistical programming activities such as designing, developing, validating, updating, and documenting SAS programs to generate analysis datasets, data listings, summary tables, and statistical graphs supporting safety and efficacy analyses. Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS.
Manager Statistical Programming Regeneron Pharmaceuticals IncManager Statistical ProgrammingCambridge, MA$128,600–$210,000 / yearAlso acceptable - 5+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry, including some project and people management experience with a Master's Degree in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline. The incumbent will be responsible for leading the programming aspect of a project, both internally or CROs, for all programming deliverables from the single study through to regulatory approval, product launch, data monitoring boards and annual reports.
Associate Director, Statistical Programming Kailera TherapeuticsAssociate Director, Statistical ProgrammingWaltham, MassachusettsProven hands-on experience in programming for clinical development, preferably in a leadership role, with a strong preference for late-phase clinical trial support. Rooted in an entrepreneurial spirit and a team-oriented culture, we are working together to advance Kailera’s mission to advance novel therapies for obesity and related conditions.
Associate Director, Statistical Programming Alkermes PlcAssociate Director, Statistical ProgrammingWaltham, MAIn 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts' Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine. The Associate Director will combine technical and project management skills to lead programmers to develop and validate SAS programs to produce high quality deliverables for in-house and outsourced projects in CDISC compliance to meet regulatory requirements.
Director, Statistical Programming CSL PlasmaDirector, Statistical ProgrammingWaltham, MassachusettsWe use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas.
ADS Programmer (Boston, On-Site) Genentech IncADS Programmer (Boston, On-Site)Boston, MA$97,100–$180,300 / yearIn addition to supporting regulatory submissions, the ADS Programmer plays a critical role in generating data insights through platforms such as the Insight Engine, enabling real-time exploration and interpretation of diverse clinical and exploratory data. We identify, influence, and adopt industry-leading digital and automation solutions, develop analytical approaches to support exploratory analyses, and align statistical programming practices across both early- and late-stage clinical development.
Biostatistical Data Programmer CorronaBiostatistical Data ProgrammerWaltham, MassachusettsSummary of Position: The Biostatistical Data Programmer will work under the guidance of a Biostatistician/Data Scientist in database management and data sciences to support the development, programming and maintenance of data, tools and processes for the Corrona data lifecycle and business integrity. Education/Experience: Required: • Bachelor’s Degree with a least 3 years’ experience or Master’s Degree plus 1 year experience in Biostatistics, Statistics, Mathematics, Applied Mathematics or Computer science with a concentration in Statistics or Mathematics.
NewManager/Senior Manager, Statistical Programming Beam Therapeutics IncManager/Senior Manager, Statistical ProgrammingCambridge, MA$130,000–$190,000 / yearManages the activities of data summary, statistical analysis, patient profile, safety and efficacy tables, listings and figures using Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL, SAS/ODS and R. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.
Associate Director, Statistical Programming Dyne Therapeutics IncAssociate Director, Statistical ProgrammingWaltham, MA$175,000–$204,000 / yearIn collaboration with cross-functional stakeholders, this role provides technical consultation to study teams and supports alignment of statistical programming resources and capabilities to meet organizational priorities. Primary Responsibilities Include: Lead and oversee statistical programming activities across multiple clinical trials and studies, ensuring high-quality deliverables, operational consistency, and adherence to timelines.
Principal Programmer ( Data Oversight & Standards) CSL Behring LLCPrincipal Programmer ( Data Oversight & Standards)MA$170,000–$201,000 / yearWe use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. Focused on serving patients' needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas.
NewManager/Senior Manager, Statistical Programming Beam TherapeuticsManager/Senior Manager, Statistical ProgrammingCambridge, MA$130,000–$190,000 / yearManages the activities of data summary, statistical analysis, patient profile, safety and efficacy tables, listings and figures using Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL, SAS/ODS and R. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.
Senior Programmer (Clinical Study) CSL Behring LLCSenior Programmer (Clinical Study)MAWe use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. Focused on serving patients' needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas.
CMM Programmer Pace IndustriesCMM ProgrammerCambridge, MA$36–$44 / hourAdditionally, the CMM Programmer supports quality improvement efforts, internal auditing, and continuous improvement initiatives, participating in project kick-off teams to enhance product introduction quality. Quality Documentation: Conduct detailed First Article Inspections (FAI) and capability studies; compile and present clear, concise data packages to support customer PPAP requirements.
NewGENETICS & GENOMICS PROGRAMMER AND DATA ANALYST School of Medicine Genetics Molecular Medicine Boston UniversityGENETICS & GENOMICS PROGRAMMER AND DATA ANALYST School of Medicine Genetics Molecular MedicineBoston, MAIn a highly collaborative environment, the successful applicant will: Implement various computational frameworks/analysis strategies for multiple ongoing and emerging genetics and genomics projects in Alzheimer disease, substance use disorders, and age-related macular degeneration involving high-throughput, next generation sequencing (NGS) datasets (e.g. The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to departmental budgets, qualifications, experience, education, licenses, specialty, training and internal pay comparison.
Metrology OGP Programmer The Procter & Gamble CoMetrology OGP ProgrammerBOSTON, MA$32–$52 / hourThe Metrology OGP Programmer will be responsible for the following tasks with minimal direction: Read and interpret prints to understand OGP program requirements, including GD&T, tolerances and datums. Procter & Gamble does not sponsor candidates for permanent residency except in some areas that in Procter & Gamble's sole discretion require highly specialized backgrounds.
Senior CNC Programmer & Machinist, 5-Axis Rennscot MFGSenior CNC Programmer & Machinist, 5-AxisWoburn, MassachusettsWorks in an active manufacturing environment subject to noise, vibration, metal chips, cutting fluids, and industrial equipment; required to wear personal protective equipment (PPE) at all times on the shop floor, including safety glasses, hearing protection, and steel-toed footwear. You have a deep, demonstrated commitment to continuous learning and technical mastery — actively monitoring industry trends, emerging technologies, and external best practices and translating findings into organizational capability advances and thought leadership.
Hiring for Sr Manufacturing Engineer / CMM Programmer at Andover, MA 01810 LanceSoft IncHiring for Sr Manufacturing Engineer / CMM Programmer at Andover, MA 01810Andover, MA$80 / hourSelf-manage workload to support existing production, perform non-recurring engineering work for new products, and drive improvement projects to completion. Support process improvements using data analysis, application of best practices, engaging with production personnel, and implementing innovative solutions to improve process capability and decrease cost.
NewGENETICS & GENOMICS PROGRAMMER AND DATA ANALYST, School of Medicine, Genetics, Molecular Medicine Boston UniversityGENETICS & GENOMICS PROGRAMMER AND DATA ANALYST, School of Medicine, Genetics, Molecular MedicineBoston, MA$62,525–$81,175Full timeImplement various computational frameworks/analysis strategies for multiple ongoing and emerging genetics and genomics projects in Alzheimer disease, substance use disorders, and age-related macular degeneration involving high-throughput, next generation sequencing (NGS) datasets (e.g. Strong programming and analytic skills in R and Python or Perl, strong scientific writing skills, and three years relevant work or graduate education experience.
Associate Director, Biostatistics Clinical Dynamix, Inc.Associate Director, BiostatisticsBurlington, MAspecific responsibilities while upholding our core working behaviors of Trust and Respect, Communication and Feedback, Accountability and Reliability, Objectivity, and Team Balance and. •Provide high-quality statistical support across clinical programs, ensuring scientific.
NewSenior Manager/Associate Director, Biostatistics Beam TherapeuticsSenior Manager/Associate Director, BiostatisticsCambridge, MA$155,000–$225,000 / yearThe ideal candidate will work closely with cross-functional study teams to provide statistical input, contribute to study-level strategy, and oversee CRO biometrics deliverables to support timely and high-quality trial execution. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.
Associate Director Biostatistics Alnylam Pharmaceuticals IncAssociate Director BiostatisticsCambridge, MA$185,300–$250,700 / yearThe Associate Director, Biostatistics is responsible for statistical activities in support of clinical trials, including contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical trial data. Our deep pipeline, late-stage programs, and bold vision reflect our core values: fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people.
Director, Biostatistics Tempus AI IncDirector, BiostatisticsMA$180,000–$240,000 / yearSalary Range: CHI: $180,000-$240,000 USD NYC/SF: $190,000-$260,000 The expected salary range above is applicable if the role is performed from California and may vary for other locations (Colorado, Illinois, New York). We are seeking a highly motivated and capable Director of Biostatistics to lead a team of biostatisticians involved in multiple aspects of clinical research at Tempus.
Director Biostatistics Alnylam Pharmaceuticals IncDirector BiostatisticsCambridge, MA$212,500–$287,500 / yearHe/she is responsible for statistical activities including: designing innovative clinical trials, authoring statistical sections of protocols, preparing statistical analysis plans, ensuring quality in implementation of statistical analysis, interpreting and communicating the results of statistical analysis of clinical trial data in support of regulatory submissions as well as manuscripts, and leading biostatistics support for worldwide regulatory submissions. Our deep pipeline, late-stage programs, and bold vision reflect our core values: fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people.
Director, Biostatistics Kymera Therapeutics IncDirector, BiostatisticsWatertown, MA$195,000–$275,000 / yearHaving advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. How you'll make an impact: As the Lead Statistician, you will spearhead the statistical efforts of a clinical program, playing a key role in the clinical development plan, regulatory submissions, and overall data strategy.
Associate Director, Clinical Trial Reporting TakedaAssociate Director, Clinical Trial ReportingMassachusettsThis Associate Director, Clinical Trial Reporting role will work on Clinical Trial Reporting activities to deliver data listings and visualizations to facilitate the delivery of high-quality data in a timely manner, leading to statistical analysis and submission to regulatory authorities. This role partners with Clinical Data Management and works with Takeda study teams to develop listings and visualizations specifications, build and/or oversee implementation of data review objectives/artifacts for clinical trials to support the overall data review plan.
NewSenior Manager/Associate Director, Biostatistics Beam Therapeutics IncSenior Manager/Associate Director, BiostatisticsCambridge, MA$155,000–$225,000 / yearThe ideal candidate will work closely with cross-functional study teams to provide statistical input, contribute to study-level strategy, and oversee CRO biometrics deliverables to support timely and high-quality trial execution. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.
Senior Statistician II - Biostatistics AstraZeneca PlcSenior Statistician II - BiostatisticsBoston, MAThe Senior Statistician II has sufficient experience working as a statistician in the pharmaceutical industry to be working independently on activities relating to design, delivery and interpretation, regulatory submissions and/or commercialisation. The accountabilities for supporting projects directly are: Provide statistical expertise for complex design and interpretation for clinical programmes, high level internal governance committees, regulatory submissions and/or commercialisation.
Director or Senior Director of Biostatistics Kymera TherapeuticsDirector or Senior Director of BiostatisticsWatertown, MA$195,000–$275,000 / yearHaving advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. As the Lead Statistician, you will spearhead the statistical efforts of one or more clinical programs, playing a key role in the clinical development plan, regulatory submissions, and overall data strategy.
Director, Biostatistics Monte Rosa Therapeutics, IncDirector, BiostatisticsBoston, MassachusettsFull timeThe Director will work closely with Clinical Development and external partners to drive trial design, analysis strategies, and regulatory‑ready outputs while remaining directly involved in study‑level statistical activities. Overview: The Director of Biostatistics is a hands‑on statistical leader responsible for the design, analysis, and interpretation of Phase 1–Phase 3 clinical trials with a primary focus on inflammation and oncology indications.
Senior Director, Biostatistics Sarepta Therapeutics IncSenior Director, BiostatisticsCambridge, MAFoster a culture where biostatisticians are hands-on analysts and scientific architects, not solely oversight managers, personally engaging with data exploration using modern tools (R, Python, interactive visualization) alongside traditional SAS workflows. The role requires a leader who can operate across both confirmatory and exploratory analytics - driving rigorous regulatory-grade deliverables while fostering a culture of rapid, hands-on data exploration in close partnership with clinical development.
Contract Clinical Trial Associate StratAcuity Staffing Partners IncContract Clinical Trial AssociateWaltham, MA$47–$52 / hourIn terms of professional development, Everforth Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA. Everforth Apex also offers a HSA (Health Savings Account on the HDHP plan), a SupportLinc Employee Assistance Program (EAP) with up to 8 free counseling sessions, a corporate discount savings program and other discounts.
Director, Biostatistics Monte Rosa Therapeutics IncDirector, BiostatisticsBoston, MAThe Director will work closely with Clinical Development and external partners to drive trial design, analysis strategies, and regulatory-ready outputs while remaining directly involved in study-level statistical activities. The Director of Biostatistics is a hands-on statistical leader responsible for the design, analysis, and interpretation of Phase 1-Phase 3 clinical trials with a primary focus on inflammation and oncology indications.
NewStudy Design Statistician (US) MMSStudy Design Statistician (US)Boston, MAFull timeWorking alongside innovative statisticians you will be responsible for leading the full life-cycle of KerusCloud support and statistical services, from: Assisting customers with their study design with a particular focus on simulation with KerusCloud to ensure they are aligned with the study objectives. As part of our Strategic Statistical Services Arm, this is a full-time role with emphasis on being an internal and external SME for clinical trial design, together with providing consultation to advise clients on a range of broader statistical issues, and will have an internal job title of Strategic Statistician .
Senior Biostatistician - Remote (US) MMSSenior Biostatistician - Remote (US)Boston, MARemoteFull timeLeads projects (all phases and even a program of studies) and smaller submissions, manages client meetings, CRMs, collaborates well with regulatory, PMs and sponsor. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive.
Principal Developer, Data Visualization and Application Development Biogen IncPrincipal Developer, Data Visualization and Application DevelopmentCambridge, MAPosition also requires 4 years of experience in the following: Developing and optimizing R programs using packages including dplyr, data.table, and tidyr to efficiently extract, transform, and analyze large datasets, integrating results for advanced statistical modeling and visualization. Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.