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SAG Aris GmbH in Spain seeks an Account Executive to drive revenue growth, acting as a strategic advisor to customers and prospects.The role involves generating qualified opportunities, winning new business, and expanding ARIS’ footprint with C-level executives.Required are 6+ years in SAS or cons

Las responsabilidades incluyen soporte y monitorización de procesos en SAS, así como el desarrollo de soluciones de datos en Azure utilizando tecnologías como Databricks, PySpark y Python. Cobser Consulting está en busca de un/a Especialista SAS con experiencia en Azure Databricks para unirse a

pSyneos Health, Inc. is looking for a Sr/Principal Statistician based in Madrid, Spain. This role involves providing statistical support across clinical projects, including the development of Statistical Analysis Plans and coordination of biostatistics activities. /ppThe ideal candidate should have a PhD/MS in statistics or a related field with at least 3 years of experience in the pharmaceutical industry, along with proficiency in SAS and R. This position may require minimal travel and offers the opportunity to mentor junior staff. /p #J-18808-Ljbffr

ph3Experteer Overview /h3 pIn this role, you help clients navigate risk through AI-driven approaches, shaping strategies and governance. You will work with cross-functional teams to embed AI into risk management, unlocking deeper insights and resilient operations. The position sits at the intersection of risk practice and advanced analytics, offering growth through structured learning and mentorship. You will contribute to client outcomes while advancing our capabilities in AI-enabled risk management. /p h3Compensaciones / Beneficios /h3 ul liCollaborate with clients to identify vulnerabilities and build long-term resilience using AI-powered tools /li liEquip clients to respond to disruptions and institutionalize enterprise risk management practices /li liLeverage AI code assistants, agentic workflows, and advanced analytics to enhance decision-making and risk mitigation /li liFor Risk Analytics: apply data-driven scenario planning, stress-testing, and advanced modeling to quantify risk exposures /li liDevelop and validate models integrating AI and Agentic technologies for deeper insights /li liFor Risk: strengthen governance and operational resilience by embedding AI into workflows and decision-making /li liGuide clients in navigating complex challenges while driving efficiency and innovation through AI adoption /li liJoin a team shaping the future of risk management with AI /li /ul h3Responsabilidades /h3 ul liMaster's degree required with a quantitative focus /li li2+ years of experience in risk management, risk analytics/modelling, or risk consultancy /li liExperience with AI agents or Agentic technologies /li liFamiliarity with machine learning/AI (NLP, deep learning, anomaly detection); GenAI/LLM a plus /li liStrong conceptual problem-solving and quantitative modeling skills /li liAbility to work collaboratively and drive independent workstreams within a team /li liExperience with risk model lifecycle (development, implementation, testing) and programming in Python, R, or similar /li liKnowledge of SQL, NoSQL, Matlab, or SAS is a strong advantage /li liExcellent communication skills in English and local language /li liWillingness to travel /li /ul pSenior Consultant - Risk Resilience Madrid, ES /p /p #J-18808-Ljbffr

ph3Die Position /h3 pAs the Lead System Architect (LSA) - Platform Architect, you will serve as the highest technical authority for the Pega Platform within the Workflow Automation team. In this strategic role, you define the enterprise class structure, lead the technical governance of the Digital Process Automation (DPA) ecosystem, and ensure all automation solutions are built for maximum reuse, scalability, and performance. You act as the primary technical consultant for the Product Owner and business stakeholders, transforming high-level business visions into robust, future-proof architectural blueprints. Define and enforce the Pega Enterprise Class Structure (ECS) and foundational architectural layers. /p pbYour Responsibilities /b /p ul liLead technical reviews for high-complexity initiatives and ensure strict adherence to development guardrails. /li liSolve complex technical challenges and architectural ambiguities, conducting feasibility studies and performance impact assessments for enterprise-wide integrations. /li liAct as the ultimate technical mentor for Senior System Architects (SSAs) and System Architects (SAs), fostering a culture of continuous learning and engineering excellence. /li liPartner closely with the Product Owner to influence the DPA roadmap from a technical feasibility and sustainability perspective. /li liOversee system health, security compliance, and performance tuning using diagnostic tools. /li liDrive the implementation of modern DevOps, CI/CD, and automated testing strategies for the platform. /li /ul pbWho You Are /b /p ul liYou are a visionary technical leader who balances immediate delivery needs with long-term platform stability. You possess a passion for challenging the status quo and driving continuous innovation in Digital Process Automation. /li liYou bring a minimum of 8–12 years in software engineering, with at least 5–7 years dedicated specifically to Pega platform architecture. /li liCertification: A valid Pega Lead System Architect (LSA) certification is a mandatory requirement for this role. /li liTrack Record: You have proven experience leading the technical architecture for large-scale, multi-stream Pega implementations in a global environment. /li liTechnical Mastery: Deep expertise in Pega Infinity (8.x/24.x) Case Management, DevOps (Deployment Manager), and Security models. /li liIntegration Performance: Expert knowledge of microservices, REST/SOAP, OAuth, and Kafka integrations, alongside advanced proficiency in diagnostic tools and database optimization. /li liInfrastructure: Strong understanding of cloud-native Pega deployments (AWS/Azure) and containerization. /li liCommunication: Excellent communication and stakeholder management skills, with a proven ability to influence senior technical leaders and navigate complex team dynamics. /li /ul pAt Roche, we aim high to deliver life-changing healthcare solutions. If you’re ready to make a meaningful impact on patients and healthcare systems worldwide, this is the place for you. /p pbRoche ist ein Arbeitgeber, der die Chancengleichheit fördert. /b /p /p #J-18808-Ljbffr

Experteer Overview As a Principal Biostatistician in a leading biopharmaceutical solutions organization, you will lead statistical activities across multiple studies and serve as the primary sponsor contact for biostatistics. You mentor and train Biostatistics staff, oversee project analytics, and ensure high-quality, compliant deliverables. You will contribute to study design, SAPs, randomization, and regulatory interactions, shaping analyses and decisions. This role offers impact across programs while aligning with Syneos Health’s mission to shorten the distance from lab to life. Compensaciones / Beneficios • Lead projects across multiple studies or programs and act as primary statistical contact for sponsors • Mentor biostatisticians, oversee training plans and sessions • Prepare and review Statistical Analysis Plans (SAPs) and mock-up displays • Oversee protocol statistics, randomization schedules, and CSRs input • Review SAS annotated CRFs, SAS databases, and data capture for quality • Create/Review programming specifications for analysis datasets, tables, listings, figures • Direct and review work of other biostatistics personnel to ensure timely, high-quality output • Ensure compliance with SOPs, WIs, and regulatory guidelines (ICH) • Participate in DSMB/DMC activities as needed; may act as independent/non-voting statistician • Lead integrated analyses and support regulatory meetings; respond to analyst questions • Maintain documentation and inspection readiness; support project deliverables timeline • Support business development with proposals, budgets, and sponsor bid defenses • Travel minimal; contribute to internal meetings and cross-functional collaboration • Maintain project quality control and verification of outputs • Provide statistical programming support where needed • Contribute to process improvements and operational solutions • Prepare for internal meetings with thoughtful contributions • Possibly engage in sponsor communications and protocol development • Ensure alignment with company objectives and quality standards • Monitor milestones and adapt to timeline changes • Escalate out-of-scope tasks to management Responsabilidades • Requisitos principales • career development • total rewards program • Total Self culture • supportive management • professional training • global collaboration

Syneos Health is seeking a Sr/Principal Statistician (Sponsor-dedicated) for the Madrid, Spain location. The role focuses on statistical leadership across drug development programs, from protocol through CSR, with a need for R/SAS expertise and strong collaboration with sponsors. The candidate should have a Ph D or MS in statistics, 3+ years of pharma experience, and proven ability to lead projects and mentor junior statisticians in a fast-paced environment. #J-18808-Ljbffr

ph3Job Overview /h3 pAs a Principal Statistical Programmer you will provide advanced technical expertise to develop process methodology for the department to meet internal and external clients’ needs across complex projects and studies. /p pThis involves planning and coordinating the development of integrated programming solutions, serving the full spectrum of statistical programming needs, and providing internal consulting services, including specifications and user needs analysis for complex project or client requirements. /p h3Key Responsibilities /h3 ul liPerform, plan, coordinate, and implement programming, testing, and documentation for complex studies. /li liDevelop and maintain statistical programs for creating tables, figures, and listings. /li liCreate derived datasets and transfer files for internal and external clients. /li liConduct quality control checks on source data and report issues periodically. /li liInterpret project requirements and develop programming specifications. /li liProvide advanced technical expertise and deliver solutions to SP teams. /li liAct as technical team lead for single or group complex studies. /li liCommunicate with statisticians and clinical team members to ensure understanding of requirements and timelines. /li liEstimate programming scope, manage resources, communicate status, and negotiate timelines. /li liUse and promote established standards, SOPs, and best practices. /li liProvide training and mentoring to SP team members. /li /ul h3Requirements /h3 ul liBachelor’s Degree in Maths, Computer Science, Statistics, or related field. /li li7+ years’ statistical programming experience within the life science industry. /li liStrong efficacy experience. /li liAdvanced knowledge of statistics, programming, and/or clinical drug development process. /li liAdvanced knowledge of Base SAS, SAS Graph, and SAS Macro. /li liAdvanced knowledge of relevant data standards such as CDISC/ADaM/SDTM. /li /ul h3Benefits /h3 ul liGlobal exposure. /li liVariety of therapeutic areas. /li liCollaborative and supportive team environment. /li liAccess to cutting‑edge in‑house technology. /li liExcellent career development and progression opportunities. /li liWork‑life balance with a focus on well‑being. /li /ul /p #J-18808-Ljbffr

ph3Sr/Principal Statistician (Sponsor-dedicated) Many possible locations (EMEA) - R Shiny experience /h3 pUpdated: Todaybr/Location: Madrid, Spainbr/Job ID: -OTHLOC-3529-2DMAD-2DR /p h3Description /h3 pSyneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. /p pOur Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. /p pWhether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. /p h3Job Responsibilities /h3 ul liProvides support across all assigned statistical tasks during the lifecycle of the project, from protocol to CSR. /li liPrepares Statistical Analysis Plans (SAPs), including development of well‑presented mock‑up displays for tables, listings, and figures. Collaborate with the sponsor, if required. /li liMay be responsible for the statistical aspects of the protocol, generation of randomization schedule, publications and input to the clinical study report. /li liCoordinates the activities of other biostatistics and statistical programming personnel on assigned projects to ensure timely completion of high quality work. Provides independent review of project work produced by other biostatisticians in the department. /li liCreates or reviews programming specifications for analysis datasets, tables, listings, and figures. /li liReviews SAS annotated case report forms (CRFs), database design, and other study documentation to ensure protocol criteria are met and all data is captured as required to support a high quality database and the planned analysis. /li liConducts and participates in verification and quality control of project deliverables, ensuring that output meets expectations and is consistent with analysis described in SAP and specifications. /li liImplements company objectives, and create alternative solutions to address business and operational challenges. /li liServes as biostatistics representative on project teams, interfacing as necessary with other departmental project team representatives. This would include preparing in advance for internal meetings, contributing ideas, and demonstrating respect for opinions of others. /li liManages scheduling and time constraints across multiple projects, sets goals based on priorities from management, adapts to timeline or priority changes by reorganizing daily workload, and proactively communicates to biostatistics management any difficulties with meeting these timelines. /li liMonitors progress on study activities against agreed upon milestones and ensures the study timelines for project deliverables are met. Identifies out of scope tasks and escalates to management. /li liProvides statistical programming support as needed. /li liMay participate in Data Safety Monitoring Board and/or Data Monitoring Committee activities, including charter development and serving as an independent non‑voting biostatistician. /li liMay lead projects involving integrated analyses, attend regulatory agency meetings or respond to questions, as needed, to support the statistical analysis results of clinical trials on behalf of the sponsor. /li liFollows applicable SOPs, WIs, and relevant regulatory guidelines (e.g. ICH). /li liMaintains well organized, complete, and up‑to‑date project documentation, and verification/quality control documents and programs; ensuring inspection readiness. /li liDisplays willingness to work with others and assists with projects and initiatives as necessary to meet the needs of the business. /li liSupports business development activities by contributing to proposals, budgets, and attending sponsor bid defense meetings. /li liCoaches and mentors other Biostatistics staff. /li liPerforms other work‑related duties as assigned. /li liMinimal travel may be required. /li /ul h3Qualifications /h3 pPhD/MS in statistics or related discipline with at least 3 years of pharmaceutical experience. Good knowledge and understanding of advanced statistical concepts and methods. Able to do advanced statistical analyses using SAS or R. Experience with meta‑analyses and late‑phase clinical trials strongly preferred. /p h3Additional Information /h3 pTasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. /p /p #J-18808-Ljbffr

TakeTalent joins PharmaMar in the search for a Clinical Pharmacology Scientist to support the development of innovative oncology therapies through cutting-edge clinical pharmacology and model-informed drug development strategies. Los candidatos deben tomarse el tiempo de leer atentamente todos los elementos de este anuncio de empleo. Por favor, envíen su solicitud sin demora. At PharmaMar, they are committed to advancing science and transforming patient outcomes through innovative oncology research. The Clinical Pharmacology team plays a critical role in early clinical development, generating the pharmacokinetic, pharmacodynamic and translational insights needed to optimize drug development and support regulatory decision-making. What will you do?- Support the implementation of Clinical Pharmacology and Early Clinical Development plans with scientific rigor and a high level of autonomy. - Provide guidance and scientific mentorship to Clinical Pharmacology Scientists and Associate Scientists within the team. - Coordinate and oversee bioanalytical activities, including sample shipment tracking, vendor management, review of validation plans, budgets and work orders. - Perform pharmacokinetic analyses, including Non-Compartmental Analysis (NCA), Population Pharmacokinetic (PopPK) analysis and Physiologically Based Pharmacokinetic (PBPK) modeling. - Conduct pharmacodynamic and PK/PD analyses to assess treatment efficacy, dose-limiting toxicities and exposure-response relationships. - Support first-in-human (FIH) studies, including ECG/Holter monitoring activities and c-QT/t-QT analyses. - Contribute to Model-Informed Drug Development (MIDD) initiatives through pharmacometric analyses, simulations and interpretation of results. - Develop and maintain high-quality analytical workflows and databases following Good Coding Practices. - Contribute to Clinical Pharmacology sections of study protocols, development plans, scientific publications and technical reports. - Provide scientific support to Regulatory Affairs activities and interactions with agencies such as the EMA and FDA. - Collaborate closely with cross-functional teams including Medical Oncology, Biostatistics, Data Management and other key stakeholders. - Participate in departmental initiatives that contribute to the overall success of Early Clinical Development programs. Position requirements - Bachelor's degree in Pharmacy, Medicine, Biology, Biotechnology or a related scientific discipline. - Master's degree and PhD in Pharmacology, Immunology, Computational Biology, Bioinformatics, Biostatistics or a related field. - Fluent English, both written and spoken. - More than 3 years of experience in clinical research, preferably within pharmacology, immunology or translational medicine. - Experience authoring scientific publications and technical reports. - Proven expertise in pharmacometric modeling tools such as NONMEM, Monolix, PK-Sim or similar platforms. - Strong programming skills in R and SAS for data analysis and process automation. - Knowledge of additional programming languages such as Python and Bash. - Experience in bioanalysis and biomarker evaluation. - Solid understanding of statistical methodologies, including descriptive, univariate and multivariate analyses. - Experience with Next-Generation Sequencing (NGS), pharmacogenetics, genotyping analyses and bioinformatics pipelines. - Excellent communication skills and the ability to work independently while contributing effectively within multidisciplinary teams. What do we offer?- Competitive annual salary and performance-based bonus. - Comprehensive benefits package, including private health insurance, employee share plan, company canteen, continuous training and development opportunities, among others. - Flexible start time (7:30h to 9:30h) and intensive working hours on Fridays. - Hybrid working model available after successfully completing the six-month probation period, combining on-site collaboration with remote work flexibility. - The opportunity to contribute to groundbreaking oncology research in an innovative and science-driven environment. xbhjioe - A strong commitment to diversity, equal opportunities and an inclusive work environment where all talent is valued and respected. If you are passionate about clinical pharmacology, translational science and innovative drug development, we would love to hear from you.

Senior Technical Architect – Managed Cloud Services- Hybrid OR Remote, France OR SpainWe’re a leader in data and AI. Through our software and services, we inspire customers around the world to transform data into intelligence – and questions into answers.About The JobWe’re a leader in data and AI. Through our software and services, we inspire customers around the world to transform data into intelligence—and questions into answers.As part of our continued growth and investment in SAS Managed Cloud Services (MCS), we are expanding our Global Enablement and Sales Support capability across EMEA and the Globe.You WillShape and influence complex opportunitiesDefine and govern architecture standards and patternsEnsure solutions are viable from pre‑sales through to delivery and operationsDrive enablement and capability uplift across global teamsYou will work closely with Customer Advisory, Professional Services, and Managed Cloud teams globally, helping to scale best practices, reduce delivery risk, and improve consistency across regions.This is a high‑visibility role with the opportunity to impact both customer success and internal capability at scale.Architecture Leadership & Solution DesignLead the design of scalable, secure, and cost‑effective SAS Managed Cloud architectures across complex opportunities.Translate business requirements into robust technical solutions aligned with customer and operational needs.Provide technical leadership within sales cycles, shaping solution strategy and deal positioning.Sales‑to‑Delivery Alignment & Risk MitigationEnsure proposed solutions are commercially viable and operationally deliverable.Act as a key bridge between sales and delivery teams to align expectations and reduce execution risk.Support successful transition from pre‑sales into implementation and managed operations.Architecture Governance & StandardsApply and promote structured architecture design processes (e.G. requirements capture, architecture artefacts, design reviews).Lead architecture validation and quality assurance activities across opportunities.Contribute to the evolution of architecture standards, patterns, and governance frameworks.Global Enablement & Capability DevelopmentLead and deliver enablement initiatives across global Sales, Customer Advisory, and Delivery teams.Develop and curate technical content within the MCS Enable platform (e.G. architecture blueprints, whitepapers, best practices).Drive adoption of new capabilities, services, and standards across regions.Reusable Assets & Thought LeadershipCreate and maintain reusable intellectual property, including:Solution blueprintsArchitecture patternsPre‑sales assets and enablement materialsContribute to internal and external thought leadership through presentations, workshops, and publicationsStakeholder Engagement & InfluenceBuild trusted relationships with Account Executives, technical stakeholders, and senior customer representativesProvide consulting‑level guidance on architecture, strategy, and best practicesInfluence deal strategy and customer direction through credible technical leadershipTeam Contribution & MentorshipMentor and support the development of less experienced architectsContribute to a culture of knowledge sharing, continuous improvement, and technical excellenceParticipate in global collaboration across regions and functional teamsRequired QualificationsBachelor’s degree in Computer Science, Engineering, or a related discipline (or equivalent experience)Significant experience in technical architecture, pre‑sales, or solution engineering rolesDeep knowledge of SAS platforms and enterprise architecture within managed cloud environmentsProven experience supporting complex, enterprise‑scale sales cyclesStrong commercial awareness and ability to align technical solutions to business outcomesExcellent communication, presentation, and stakeholder engagement skillsAbility to operate effectively in a global, matrixed environmentEquivalent combination of related education, training and experience may be considered in place of the above qualifications.Additional Competencies, Knowledge And SkillsAdaptability – Maintaining effectiveness when experiencing major changes in work responsibilities or environment (e.G., people, processes, structure, or culture); adjusting effectively to change by exploring the benefits, trying new approaches, and collaborating with others to make the change successful.Communication – Conveying information and ideas clearly and concisely to individuals or groups in an engaging manner that helps them understand and retain the message; listening actively to others.Decision Making – Identifying and understanding problems and opportunities by gathering, analyzing, and interpreting quantitative and qualitative information; choosing the bestcourse of action by establishing clear decision criteria, generating and evaluating alternatives, and making timely decisions; taking action that is consistent with available facts and constraints and optimizes probable consequenceYou are welcome here.At SAS, it’s not about fitting into our culture – it’s about adding to it. We believe our people make the difference. Our inclusive workforce brings together unique talents and inspires teams to create amazing software that reflects the diversity of our users and customers.#J-18808-Ljbffr

Experteer Overview In this role, you help clients navigate risk through AI-driven approaches, shaping strategies and governance. You will work with cross-functional teams to embed AI into risk management, unlocking deeper insights and resilient operations. The position sits at the intersection of risk practice and advanced analytics, offering growth through structured learning and mentorship. You will contribute to client outcomes while advancing our capabilities in AI-enabled risk management. Compensaciones / Beneficios • Collaborate with clients to identify vulnerabilities and build long-term resilience using AI-powered tools • Equip clients to respond to disruptions and institutionalize enterprise risk management practices • Leverage AI code assistants, agentic workflows, and advanced analytics to enhance decision-making and risk mitigation • For Risk Analytics: apply data-driven scenario planning, stress-testing, and advanced modeling to quantify risk exposures • Develop and validate models integrating AI and Agentic technologies for deeper insights • For Risk: strengthen governance and operational resilience by embedding AI into workflows and decision-making • Guide clients in navigating complex challenges while driving efficiency and innovation through AI adoption • Join a team shaping the future of risk management with AI Responsabilidades • Master's degree required with a quantitative focus • 2+ years of experience in risk management, risk analytics/modelling, or risk consultancy • Experience with AI agents or Agentic technologies • Familiarity with machine learning/AI (NLP, deep learning, anomaly detection); GenAI/LLM a plus • Strong conceptual problem-solving and quantitative modeling skills • Ability to work collaboratively and drive independent workstreams within a team • Experience with risk model lifecycle (development, implementation, testing) and programming in Python, R, or similar • Knowledge of SQL, NoSQL, Matlab, or SAS is a strong advantage • Excellent communication skills in English and local language • Willingness to travel Requisitos principales •

pSAS in Madrid is seeking an Account Executive – Customer Intelligence to drive growth across Financial Services, Retail, Communications and Energy. You will own end-to-end sales cycles for a portfolio of customers and prospects, collaborating with internal teams to craft value-led proposals and close complex deals. /ppThe role blends startup agility with enterprise scale, offering hybrid work and opportunities to influence strategy across industries. /p #J-18808-Ljbffr

Experteer Overview In this role you drive statistical and psychometric work to develop scoring rules, validate COA instruments, and support new endpoints. You will collaborate across the PACT and ILS u0026amp; PASS teams to ensure rigorous methods and robust data interpretation. You’ll work with real-world and digital health data, contribute to the COA Accelerator, and engage in thought leadership and publications. This position offers a chance to shape patient-centered measures and advance COA science within IQVIA. Compensaciones / Beneficios • Empirically develop scoring rules and algorithms for existing COA measures; generate scoring documentation for new instruments and simulate datasets • Provide statistical support for development of new COA measures and endpoints, including classical and modern psychometrics and time-series analysis on high-frequency data • Support the COA Accelerator tool as a statistics/psychometrics SME and review content for client subscriptions • Contribute to thought leadership through research and publications, and present findings at conferences Responsabilidades • Statistical and psychometric research skills • Strong computer skills including SAS and R • Excellent written and oral communication; attention to detail; initiative and quality focus • Ability to work in a team, communicate with internal and external teams, and manage multiple tasks in a fast-paced environment • Extensive familiarity with AI tools and their application to COA/DHT topics Requisitos principales •

Applications EngineerWe are seeking a highly motivated Applications Engineer to join our team in Spain. This is a permanent position offering the opportunity to work at the leading edge of technical solution delivery and system integration.The successful candidate will play a key role in the development, testing, and optimisation of engineering applications, with a focus on enhancing functionality and performance for demanding engineering applications. You will be part of a multidisciplinary team bridging the gap between concept and production-ready solutions. This role offers long-term career growth and the opportunity to shape the implementation of innovative vehicle platforms.All applicants must be eligible to work in Spain.Responsibilities / What you will do- Lead and support the deployment of new software and hardware applications, with emphasis on integration and advanced alloy manufacturing workflows.- Characterise and optimise application performance (e.G., reliability, user efficiency, thermal performance, and system compatibility).- Conduct experimental testing and analysis of application feedstocks and integrated systems.- Collaborate with process engineers and design teams to ensure application performance aligns with end‑use applications.- Develop and maintain technical databases, test standards, and qualification processes for new applications.- Support R&D projects, contributing to technical reports, publications, and presentations for clients.- Stay current with emerging applications, technologies, and industry standards in related manufacturing methods.Experience / Who you are- Bachelor’s degree (or higher) in Engineering, Computer Science, or a related technical field.- Proven experience in technical applications development or systems engineering within a manufacturing context.- Strong background in physical and functional characterisation (mechanical, thermal, or system analysis).- Hands‑on experience with testing techniques and validation tools for complex engineering systems.- Ability to design and execute experiments, interpret data, and draw actionable conclusions for stakeholders.- Proficiency in technical reporting and the ability to communicate results to both technical and non‑technical stakeholders.- Knowledge of how applications interact with design (DfAM) and material‑process behaviors.- Familiarity with simulation tools (FEA) or engineering software for testing application behavior.- Experience with quality systems and qualification frameworks, such as aerospace or automotive standards.#J-18808-Ljbffr

pSAS is seeking a Senior Technical Architect for its Managed Cloud Services. You will drive architecture leadership across global opportunities, translating requirements into robust SAS solutions and aligning sales with delivery to reduce risk. /ppThe role spans hybrid or remote work across France or Spain, with emphasis on scalable, secure cloud architectures. In this high‑visibility position, you’ll enable global teams, develop reusable assets, and influence deal strategy through technical /p #J-18808-Ljbffr

pRTX is seeking a skilled airport services professional to act as the on-site escalation point for Managed Services at MAD Airports. You will assess and resolve customer issues, coordinate equipment servicing and configurations, and engage with Collins Aerospace and airport operators to ensure strict adherence to customer specs. /ppThe role requires strong English and Spanish communication, problem-solving ability, and willingness to travel. /p #J-18808-Ljbffr

TakeTalent joins PharmaMar in the search for a Clinical Pharmacology Scientist to support the development of innovative oncology therapies through cutting-edge clinical pharmacology and model-informed drug development strategies. Los candidatos deben tomarse el tiempo de leer atentamente todos los elementos de este anuncio de empleo. Por favor, envíen su solicitud sin demora. At PharmaMar, they are committed to advancing science and transforming patient outcomes through innovative oncology research. The Clinical Pharmacology team plays a critical role in early clinical development, generating the pharmacokinetic, pharmacodynamic and translational insights needed to optimize drug development and support regulatory decision-making. What will you do? • Support the implementation of Clinical Pharmacology and Early Clinical Development plans with scientific rigor and a high level of autonomy., • Provide guidance and scientific mentorship to Clinical Pharmacology Scientists and Associate Scientists within the team., • Coordinate and oversee bioanalytical activities, including sample shipment tracking, vendor management, review of validation plans, budgets and work orders., • Perform pharmacokinetic analyses, including Non-Compartmental Analysis (NCA), Population Pharmacokinetic (PopPK) analysis and Physiologically Based Pharmacokinetic (PBPK) modeling., • Conduct pharmacodynamic and PK/PD analyses to assess treatment efficacy, dose-limiting toxicities and exposure-response relationships., • Support first-in-human (FIH) studies, including ECG/Holter monitoring activities and c-QT/t-QT analyses., • Contribute to Model-Informed Drug Development (MIDD) initiatives through pharmacometric analyses, simulations and interpretation of results., • Develop and maintain high-quality analytical workflows and databases following Good Coding Practices., • Contribute to Clinical Pharmacology sections of study protocols, development plans, scientific publications and technical reports., • Provide scientific support to Regulatory Affairs activities and interactions with agencies such as the EMA and FDA., • Collaborate closely with cross-functional teams including Medical Oncology, Biostatistics, Data Management and other key stakeholders., • Participate in departmental initiatives that contribute to the overall success of Early Clinical Development programs. Position requirements • Bachelor's degree in Pharmacy, Medicine, Biology, Biotechnology or a related scientific discipline., • Master's degree and PhD in Pharmacology, Immunology, Computational Biology, Bioinformatics, Biostatistics or a related field., • Fluent English, both written and spoken., • More than 3 years of experience in clinical research, preferably within pharmacology, immunology or translational medicine., • Experience authoring scientific publications and technical reports., • Proven expertise in pharmacometric modeling tools such as NONMEM, Monolix, PK-Sim or similar platforms., • Strong programming skills in R and SAS for data analysis and process automation., • Knowledge of additional programming languages such as Python and Bash., • Experience in bioanalysis and biomarker evaluation., • Solid understanding of statistical methodologies, including descriptive, univariate and multivariate analyses., • Experience with Next-Generation Sequencing (NGS), pharmacogenetics, genotyping analyses and bioinformatics pipelines., • Excellent communication skills and the ability to work independently while contributing effectively within multidisciplinary teams. What do we offer? • Competitive annual salary and performance-based bonus., • Comprehensive benefits package, including private health insurance, employee share plan, company canteen, continuous training and development opportunities, among others., • Flexible start time (7:30h to 9:30h) and intensive working hours on Fridays., • Hybrid working model available after successfully completing the six-month probation period, combining on-site collaboration with remote work flexibility., • The opportunity to contribute to groundbreaking oncology research in an innovative and science-driven environment. xkdbapo, • A strong commitment to diversity, equal opportunities and an inclusive work environment where all talent is valued and respected. If you are passionate about clinical pharmacology, translational science and innovative drug development, we would love to hear from you.

Die Position As the Lead System Architect (LSA) - Platform Architect, you will serve as the highest technical authority for the Pega Platform within the Workflow Automation team. In this strategic role, you define the enterprise class structure, lead the technical governance of the Digital Process Automation (DPA) ecosystem, and ensure all automation solutions are built for maximum reuse, scalability, and performance. You act as the primary technical consultant for the Product Owner and business stakeholders, transforming high-level business visions into robust, future-proof architectural blueprints. Define and enforce the Pega Enterprise Class Structure (ECS) and foundational architectural layers. Your Responsibilities Lead technical reviews for high-complexity initiatives and ensure strict adherence to development guardrails. Solve complex technical challenges and architectural ambiguities, conducting feasibility studies and performance impact assessments for enterprise-wide integrations. Act as the ultimate technical mentor for Senior System Architects (SSAs) and System Architects (SAs), fostering a culture of continuous learning and engineering excellence. Partner closely with the Product Owner to influence the DPA roadmap from a technical feasibility and sustainability perspective. Oversee system health, security compliance, and performance tuning using diagnostic tools. Drive the implementation of modern Dev Ops, CI/CD, and automated testing strategies for the platform. Who You Are You are a visionary technical leader who balances immediate delivery needs with long-term platform stability. You possess a passion for challenging the status quo and driving continuous innovation in Digital Process Automation. You bring a minimum of 8–12 years in software engineering, with at least 5–7 years dedicated specifically to Pega platform architecture. Certification: A valid Pega Lead System Architect (LSA) certification is a mandatory requirement for this role. Track Record: You have proven experience leading the technical architecture for large-scale, multi-stream Pega implementations in a global environment. Technical Mastery: Deep expertise in Pega Infinity (8.X/24.X) Case Management, Dev Ops (Deployment Manager), and Security models. Integration & Performance: Expert knowledge of microservices, REST/SOAP, OAuth, and Kafka integrations, alongside advanced proficiency in diagnostic tools and database optimization. Infrastructure: Strong understanding of cloud-native Pega deployments (AWS/Azure) and containerization. Communication: Excellent communication and stakeholder management skills, with a proven ability to influence senior technical leaders and navigate complex team dynamics. At Roche, we aim high to deliver life-changing healthcare solutions. If you’re ready to make a meaningful impact on patients and healthcare systems worldwide, this is the place for you. Roche ist ein Arbeitgeber, der die Chancengleichheit fördert. #J-18808-Ljbffr

Job ResponsibilitiesServes as a statistical department resource, mentors biostatisticians on job skills, oversees or develops training plans or materials for Biostatistics associates. Conducts training sessions, or otherwise trains new hires and enhances the skills of existing personnel.Prepares Statistical Analysis Plans (SAPs), including development of well‑presented mock‑up displays for tables, listings, and figures. Collaborates with sponsor, if required.Responsible for the statistical aspects of the protocol, generation of randomization schedule, and input to the clinical study report.Reviews SAS annotated case report forms (CRFs), SAS database design, and other study documentation to ensure protocol criteria are met and all data is captured as required to support a high‑quality database and the planned analysis.Creates or reviews programming specifications for analysis datasets, tables, listings, and figures.Directs the activities of other biostatistics personnel on assigned projects to ensure timely completion of high‑quality work. Provides independent review of project work produced by other statisticians in the department.Implements company objectives, and creates alternative solutions to address business and operational challenges.Serves as biostatistics representative on project teams, interfacing as necessary with other departmental project team representatives. Includes preparing in advance for internal meetings, contributing ideas, and demonstrating respect for opinions of nducts and participates in verification and quality control of project deliverables, ensuring that output meets the expected results and is consistent with analysis described in SAP and specifications.Manages scheduling and time constraints across multiple projects, sets goals based on priorities from management, discusses time estimates for completion of study‑related activities with biostatistics management, adapts to timeline or priority changes by reorganizing daily workload, and proactively communicates to biostatistics management any difficulties with meeting these timelines. Monitors progress on study activities against agreed‑upon milestones and ensures the study timelines for project deliverables are met. Identifies out‑of‑scope tasks and escalates to management.Provides statistical programming support as needed.May participate in Data Safety Monitoring Board (DSMB) and/or Data Monitoring Committee (DMC) activities, including charter development and serving as an independent non‑voting biostatistician. May serve as a voting statistician on DSMBs and/or DMCs.Leads projects involving integrated analyses, attends regulatory agency meetings or responds to questions, as needed, to support the statistical analysis results of clinical trials on behalf of the sponsor.Provides input, reviews, and subsequently follows applicable Standard Operating Procedures (SOPs), Work Instructions (WIs), and relevant regulatory guidelines (e.G., International Conference on Harmonization (ICH)).Maintains well‑organized, complete, and up‑to‑date project documentation, and verification/quality control documents and programs; ensuring inspection readiness.Displays willingness to work with others and assists with projects and initiatives as necessary to meet the needs of the business.Prepares in advance for internal meetings, contributes ideas, and demonstrates respect for opinions of others.Supports business development activities by contributing to proposals, budgets, and attending sponsor bid defense meetings.Performs other work‑related duties as assigned.Minimal travel may be required.SummaryThis position is responsible for leading projects across multiple studies or programs. A Principal Biostatistician acts as the primary contact with the sponsor for all biostatistics related activities on assigned projects. Provides external statistical consultancy for sponsor companies, and serves as a departmental resource for complex statistical questions, study design considerations, and protocol development. Core Responsibilities.Additional InformationTasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Full-time Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. Job Description You will contribute to statistical activities related to global clinical trials and work closely with international teams of statisticians, programmers and data managers, including the role of biostatistics project lead. In this role, you will: Act as a communication line for project teams, clients, vendors and internal team on statistical questions Conduct statistical analysis for clinical trials including, interim analysis, final analysis, analysis for DSMBs/DMCs and PK analysis Develop and review study protocols, statistical analysis plans, analysis dataset specifications according to CDISC ADa M standard and other project-specific documents Review statistical deliverables such as tables, figures, listings and analysis datasets Conduct departmental induction course and project-specific training for statisticians and SAS programmers Prepare for and attend internal and external study audits pertinent to Statistics Participate in preparation of internal/external audits follow up Provide input to standard operating procedures and other Quality Systems Documents (QSDs) pertinent to activities of Biostatistics Liaise with DM on statistical questions related to data issues Participate in bid defense and in kick-off meetings Lead teams of SAS programmers and/or statisticians on the project level Qualifications MSc in Statistics or equivalent Full working proficiency in English Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research Expert knowledge and understanding of the SAS programming Expert knowledge and understanding of CDISC ADa M standard Expert knowledge and understanding of pharmacokinetics principles, concepts, methods and standards used in clinical research, including the conduct NCL and population PK analysis Expert knowledge and understanding of Phoenix Win Nonlin and NLME #J-18808-Ljbffr

IQVIA is seeking a motivated HTA Analyst-Programmer in Madrid to contribute to health technology assessments and market access activities in Germany. The ideal candidate will have a Master’s degree or Ph D in biostatistics or related fields and at least 2 years of experience in advanced SAS programming.The role requires strong analytical skills and fluency in German and English, as the candidate will collaborate with cross-functional teams to ensure quality in outcomes and programming of statistical analyses.

pIQVIA is seeking a skilled statistician/psychometric researcher to advance COA instruments and real‑world evidence projects in Madrid. You will develop scoring rules, run simulations, and provide statistical support across teams. /ppIdeal candidates hold an advanced degree in statistics or psychometrics, have experience with SAS and R, and can communicate clearly with multidisciplinary groups in a fast-paced consulting environment. /p #J-18808-Ljbffr

Una compañía de tecnología financiera busca incorporar 3 perfiles Mid-Level para cubrir roles especializados en áreas regulatorias dentro del sector bancario. Se requiere un mínimo de 4 años de experiencia, habilidades analíticas avanzadas y conocimiento en SQL y SAS. La modalidad de trabajo es híbrida, y el candidato debe demostrar autonomía y capacidad de trabajo en entornos complejos. Se valorará conocimiento en tecnologías Cloud y participación en programas de transformación. La ubicación preferida es Madrid.br#J-18808-Ljbffr

Experteer Overview As Sr/Principal Statistician, you will lead statistical activities across drug development programs for sponsor-dedicated projects. You collaborate with cross-functional teams within the Clinical Solutions group to shape SAPs, study design, and analysis plans, while ensuring regulatory compliance and quality. You drive analyses, mentoring, and timely delivery of high-quality statistical outputs that support pivotal clinical decisions and regulatory submissions. This role offers impact across late-stage trials and potential DMC/DSMB activities in a globally connected environment. Compensaciones / Beneficios • Support statistical tasks across the project lifecycle from protocol to CSR • Prepare SAPs with mock-ups for tables, listings, and figures; collaborate with sponsor when required • Lead statistical aspects of protocols, randomization, publications, and input to CSR • Coordinate biostatistics and statistical programming teams for timely, high-quality work • Create/review programming specs for analysis datasets, tables, listings, and figures • Review CRFs, database design, and study docs to ensure data capture aligns with SAP • QC of deliverables to ensure alignment with SAP and specs • Represent biostatistics on project teams; prepare for internal meetings and contribute ideas • Manage scheduling and timelines across multiple projects; escalate issues to management • Monitor study progress against milestones and adjust as needed • Provide statistical programming support; participate in DMC/DSMB activities when applicable • Lead integrated analyses and participate in regulatory meetings as needed • Follow SOPs, WIs, and regulatory guidelines (ICH) and maintain ready documentation • Support business development through proposals and sponsor bid defense meetings • Coach and mentor Biostatistics staff; perform other duties as assigned • Occasional travel as required Responsabilidades • PhD or MS in statistics or related discipline with at least 3 years of pharmaceutical experience • Strong knowledge of advanced statistical concepts and methods • Proficiency in SAS or R for advanced analyses • Experience with meta-analyses and late-phase clinical trials preferred • Ability to lead projects and coordinate cross-functional teams • Familiarity with regulatory standards (ICH) and study documentation requirements • Effective communication and collaboration with sponsors and internal teams Requisitos principales • career development • supportive line management • technical and therapeutic training • peer recognition • total rewards program

Pennylane SAS is seeking an Engineering Manager in Madrid for a full-time on-site position. You will lead and mentor a squad of 5–8 Software Engineers, while collaborating closely with product managers to ensure high standards of quality and efficiency. Ideal candidates will have a minimum of 5 years in software development, preferably with Ruby on Rails or React.js, and proven management experience. Pennylane offers a competitive compensation package, remote work from anywhere in Europe, and various employee benefits. #J-18808-Ljbffr

A leading pharmaceutical company is seeking a skilled professional to oversee clinical trials and data analysis in a hybrid role based in Madrid. With a PhD in a relevant field and over 10 years of experience, you will set strategic directions and design trials, contributing significantly to innovative treatment options. Fluency in English and experience with statistical software like SAS and R are essential for this impactful position. Join a multicultural team committed to advancing health solutions.br#J-18808-Ljbffr

Data Engineer AWS (m/f/d)### Resumen del puestoBARCELONA### Modelo de trabajoHíbrido · 3 días en casahace 2 díasDescripción del puestoAbout the JobAre you interested in contributing to the development and maintenance of complex Datamarts? Are you agile, innovative, dynamic, and ready to implement challenging projects in a cloud-based environment? Are you motivated to work in an experienced team and collaborate across the community with other units of the company?Do you enjoy working in a team as well as handling independent tasks and, if necessary, following up with your interfaces to ensure progress? If you answer these questions with "Yes", then we have an interesting task for you.Our team is responsible for development and maintenance of the Datamarts for Allianz P&C insurance company. The legacy systems are based on SAS (on Linux) and Oracle DBMS and are currently in migration to AWS cloud (based on Snowflake/DBT).What you do Collaboration in all phases of projects, possibly also leading subprojects. Professional consulting of clients regarding current production and future solution possibilities, and the development of new solution concepts. Implementation of migration use cases (partially by support of AI tool assistants). Participation in the transformation of datamarts towards a cloud-based technology.What you bring A degree in Mathematics or (Business) Computer Science or a comparable qualification. Strong knowledge of agile methodologies, techniques, and processes coupled with conceptual thinking for targeted, results-oriented work. Willingness and ability to participate in complex IT projects. Structured and analytical approach, confident and assertive demeanor, strong communication and teamwork skills, strong service and customer orientation. Good English language skills, both spoken and written (CEF Level B) with the ability to clearly articulate and visually present complex issues both verbally and in writing. Good knowledge and experience with: Jenkins, DBT, Snowflake, Github as well as a good knowledge of cloud-based technologies, applications in the AWS environment. And AWS Marketplace. Experience and good knowledge in cloud development environments; proven multi-year, successful participation in (cloud) projects.* We welcome candidates with an interest in machine learning.What we offer We offer a hybrid work model which recognizes the value of striking a balance between in-person collaboration and remote working incl. up to 25 days per year working from abroad. We believe in rewarding performance and our compensation and benefits package includes a company bonus scheme, pension, employee shares program and multiple employee discounts (details vary by location). From career development and digital learning programs to international career mobility, we offer lifelong learning for our employees worldwide and an environment where innovation, delivery and empowerment are fostered. Flexible working, health and wellbeing offers (including healthcare and parental leave benefits) support to balance family and career and help our people return from career breaks with experience that nothing else can teach.About Allianz TechnologyWith its headquarters in Munich, Germany, Allianz Technology is Allianz's global IT service provider and delivers IT solutions that drive the group's digitalization. With more than 11,000 employees in over 20 countries around the world, Allianz Technology is tasked to run, optimize, transform and innovate the infrastructure, applications and services together with Allianz companies to co-create the best customer experience.We service the entire spectrum of digitalization -- from one of the industry's largest IT infrastructure projects that spans data centres, networks and security, to application platforms ranging from workplace services to digital interaction.In short: We deliver comprehensive end-to-end IT solutions for Allianz in the digital age. We are the backbone of Allianz.Find us at: www.Linkedin.Com/company/allianz-technology.Commitment to Integrity, Fairness & InclusionAllianz Group is one of the most trusted insurance and asset management companies in the world. Caring for our employees, their ambitions, dreams and challenges, is what makes us a unique employer. Together we can build an environment where everyone feels empowered and has the confidence to explore, to grow and to shape a better future for our customers and the world around us.We at Allianz believe in a strong inclusive culture that encourages people to speak their minds, get involved and question the status quo. We are proud to be an equal opportunity employer and encourage you to bring your whole self to work, no matter where you are from, what you look like, who you love, or what you believe in. We therefore welcome applications regardless of race, ethnicity or cultural background, age, gender, nationality, religion, social class, disability, sexual orientation, or any other characteristics protected under applicable local laws and regulations.To Recruitment AgenciesAllianz Technology has an in-house recruitment team that sources great candidates directly. Therefore, Allianz Technology does not accept unsolicited resumes from agencies or search firm recruiters.When we do work with recruitment agencies, that engagement is formalized by a contract. Fees will only be paid when there is a contract in place. Without a contract in place, we will not accept invoices on unsolicited resumes, even if the candidate was ultimately employed by Allianz.99149 | Data & AI | Professional | Non-Executive | Allianz Technology | Full-Time | Permanent#J-18808-Ljbffr

Amaris Consulting is seeking a Consultant in Health Economics and HTA to join our dynamic team in Barcelona. You will act as a lead analyst on health economics projects, including ITC, NMA, and Real World Evidence studies, interfacing with clients and coordinating a delivery team.The role requires an advanced degree in statistics or related field, 3+ years of experience in statistics or RWE, and strong programming skills in R or SAS.#J-18808-Ljbffr

Sr/Principal Statistician (Sponsor-dedicated) Many possible locations (EMEA) - R Shiny experience Updated: TodayLocation: Madrid, SpainJob ID: 25109875-OTHLOC-3529-2 DMAD-2 DR Description Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. Job Responsibilities Provides support across all assigned statistical tasks during the lifecycle of the project, from protocol to CSR. Prepares Statistical Analysis Plans (SAPs), including development of well‑presented mock‑up displays for tables, listings, and figures. Collaborate with the sponsor, if required. May be responsible for the statistical aspects of the protocol, generation of randomization schedule, publications and input to the clinical study report. Coordinates the activities of other biostatistics and statistical programming personnel on assigned projects to ensure timely completion of high quality work. Provides independent review of project work produced by other biostatisticians in the department. Creates or reviews programming specifications for analysis datasets, tables, listings, and figures. Reviews SAS annotated case report forms (CRFs), database design, and other study documentation to ensure protocol criteria are met and all data is captured as required to support a high quality database and the planned analysis. Conducts and participates in verification and quality control of project deliverables, ensuring that output meets expectations and is consistent with analysis described in SAP and specifications. Implements company objectives, and create alternative solutions to address business and operational challenges. Serves as biostatistics representative on project teams, interfacing as necessary with other departmental project team representatives. This would include preparing in advance for internal meetings, contributing ideas, and demonstrating respect for opinions of others. Manages scheduling and time constraints across multiple projects, sets goals based on priorities from management, adapts to timeline or priority changes by reorganizing daily workload, and proactively communicates to biostatistics management any difficulties with meeting these timelines. Monitors progress on study activities against agreed upon milestones and ensures the study timelines for project deliverables are met. Identifies out of scope tasks and escalates to management. Provides statistical programming support as needed. May participate in Data Safety Monitoring Board and/or Data Monitoring Committee activities, including charter development and serving as an independent non‑voting biostatistician. May lead projects involving integrated analyses, attend regulatory agency meetings or respond to questions, as needed, to support the statistical analysis results of clinical trials on behalf of the sponsor. Follows applicable SOPs, WIs, and relevant regulatory guidelines (e.G. ICH). Maintains well organized, complete, and up‑to‑date project documentation, and verification/quality control documents and programs; ensuring inspection readiness. Displays willingness to work with others and assists with projects and initiatives as necessary to meet the needs of the business. Supports business development activities by contributing to proposals, budgets, and attending sponsor bid defense meetings. Coaches and mentors other Biostatistics staff. Performs other work‑related duties as assigned. Minimal travel may be required. Qualifications Ph D/MS in statistics or related discipline with at least 3 years of pharmaceutical experience. Good knowledge and understanding of advanced statistical concepts and methods. Able to do advanced statistical analyses using SAS or R. Experience with meta‑analyses and late‑phase clinical trials strongly preferred. Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. #J-18808-Ljbffr

AI Enablement Localization Specialist- Hybrid, based Madrid or BarcelonaWe’re a leader in data and AI. Through our software and services, we inspire customers around the world to transform data into intelligence – and questions into answers.If you’re looking for a dynamic, fulfilling career with flexibility and a world-class employee experience, you’ll find it here. We are recognized worldwide for our inclusive, meaningful culture and innovative technologies by organizations such as Fast Company, Forbes, and Newsweek.About the jobThe Global Experience team is seeking an AI Enablement Localization Specialist to own and evolve multilingual AI and MT solutions, including terminology governance, multilingual AI enablement, and MT/LLM quality across global products. This role focuses on guiding the multilingual aspects of AI‑enabled solutions, owning translation solutions and workflows, evolving linguistic knowledge assets, and ensuring consistent, high‑quality multilingual output at scale through data‑driven evaluation and continuous improvement. The role acts as a primary owner of the multilingual aspects of AI‑enabled solutions, working closely with Product, Documentation, Engineering, and vendor teams so that multilingual AI capabilities are designed, implemented, and integrated into products and customer‑facing experiences.As a AI Enablement Localization Specialist, you will:Terminology & Knowledge Assets- Create, manage and evolve glossaries, style guides, and other linguistic and cultural assets- Design and own the terminology extraction process for products- Drive a cross‑functional effort to maintain a central terminology database (Publications team, Marketing, Products)- Govern multilingual term bases as a single source of truth for AI and MT, ensuring consistency between glossary and TM translations- Collaborate with multilingual vendors and in‑house teams to optimize workflows, translation memory, and terminology managementMachine Translation/AI and Model Evaluations- Maintain and prepare glossary assets for MT trainings and LLM RAG- Own MT and LLM engine strategy, including selection, training approach, benchmarking methodology, and evaluation- Own the design, selection, and evolution of translation solutions, including MT, LLM‑based translation, and hybrid workflows used across products and translation pipelines- Determine when shared translation solutions can be reused across product and workflow contexts, and when differentiated approaches are required- Measure MT or LLM output quality on a regular basis per locale for 20+ languages; create and execute improvement plans when scores fall beyond a threshold- Design and test various localization workflow improvements by using AI (such as APE, LQE and LQA)Quality Evaluation- Collect feedback from various stakeholders to establish end quality requirements- Define evaluation frameworks to assess both raw MT/AI and post‑edited translation quality- Implement evaluation framework and monitor performance per locale- Develop and execute improvement plans when quality standards are not metMultilingual AI Cross‑functional Enablement- Partner with Product, Docs, and Engineering teams to define and guide the multilingual aspects of AI‑enabled features, ensuring language quality, consistency and scalability requirements are met as solutions are implemented into products and customer‑facing experiences- Lead multilingual AI capabilities testing and ensure it adheres to company standards, terminology, and tone of voice; provide recommendationsfor model improvements if needed- Ensure all applicable security policies and processes are followed to support the organization’s secure software development goals- Embrace curiosity, passion, authenticity and accountability. These are our values and influence everything we doRequired qualifications- Minimum of 5 years of experience in a localization terminologist, machine translation and/or multilingual AI focused role, ideally in a stakeholder or client‑facing environment- Bachelor’s degree required, preferably in Linguistics, Computer Science or related fields; master’s a plus- Expertise in Machine Learning, LLMs, NLP, process automation and technology, with data‑analytical skills to drive great customer experience- Experience with building and maintaining terminology databases- Experience evaluating machine translation quality using automated metrics such as edit distance, BLEU and COMET, interpreting results to guide MT and LLM quality decisions- Experience setting up and using linguistic quality frameworks, managing quality control processes for linguistic outputs, ensuring adherence to high‑quality standards- Experience using localization technology (TMS/CAT tools, machine translation, LLMs) and processes, particularly for CICD software deployment model- Proficiency in additional language(s)- Proven ability to solve complex linguistic and technical challenges, with attention to detail- Ability to measure, analyze and present data to stakeholders- Ability to adjust working hours to accommodate a variety of time zones- Equivalent combination of related education, training and experience may be considered in place of the above qualificationsAdditional competencies, knowledge and skills- Quality orientation: Accomplishing tasks by considering all areas involved, showing concern for all aspects of the job and accurately checking processes and tasks over time- Communication: Conveying information and ideas clearly and concisely to individuals or groups in an engaging manner that helps them understand and retain the message; listening actively to others- Collaboration: Working cooperatively with others to help a team or work group achieve its goals- Experience using project management tools (e.G. Jira) and source management systems (e.G. Git Hub)- Programming skills are a plus (Python, SQL, My SQL)Benefits highlights- Our Recreation and Fitness Center offers recorded fitness classes to help you fit movement into your day- SAS supports your well‑being with programs that reduce stress and distractions to help you stay healthy and productive

Pennylane SAS is seeking an Engineering Manager to lead a team of software engineers remotely across Europe. The ideal candidate will possess over 5 years of software development experience, preferably in Ruby on Rails or React.Js, along with solid management skills. The mission includes managing team dynamics while collaborating closely with product managers to ensure a quality engineering process. Pennylane offers a supportive remote-first culture, competitive compensation, and numerous employee benefits aimed at enhancing work-life balance. #J-18808-Ljbffr

ph3Responsibilities /h3 ul liMonitor the credit risk quality, pricing and profitability of the credit risk portfolios of Digital Banks /li liContribute to define the new risk policies and changes in these /li liDrive the strategic management and profitability of retail portfolios /li liArchitect and refine credit risk admission policies /li liSpearhead the development of pricing strategies /li liOversee risk models and data quality /li liPrepare and refine data to ensure high quality and robustness for analysis /li /ul h3Qualifications /h3 ul liDegree in Economics, Mathematics, Physics, or Statistics /li liMaster’s level knowledge of Data Science /li liAt least 4 years of experience in Risk Management, with a focus on credit risk and retail portfolios /li liKnowledge of Credit risk management in terms of admission, recoveries, credit scoring, income estimators, and limit allocation /li liDeep understanding of credit risk models /li liBasic programming knowledge in at least one of the following: Python (PySpark, pandas, scikit-learn, Keras), R, SAS, or SQL /li liStrong analytical mindset, willingness to learn, and motivation to develop expertise in credit risk management and new markets for BBVA /li liEnglish required /li /ul /p #J-18808-Ljbffr

ppMetyis is growing! We are looking for a Data Science Associate with +4 years of experience to join our international Data and Analytics team, based in Barcelona. /pbr/h3Who we are: /h3pMetyis is a global and forward-thinking firm operating across a wide range of industries, developing and delivering Big Data, Digital Commerce, Marketing Design solutions and Advisory services. At Metyis, our long-term partnership model brings long-lasting impact and growth to our business partners and clients through extensive execution capabilities. /ppWith our team, you can experience a collaborative environment with highly skilled multidisciplinary experts, where everyone has room to build bigger and bolder ideas. Being part of Metyis means you can speak your mind and be creative with your knowledge. Imagine the things you can achieve with a team that encourages you to be the best version of yourself. /ppWe are Metyis. Partners for Impact. /ph3What we offer /h3ullipInteract with senior stakeholders at our clients on regular basis to drive their business towards impactful change /p /lilipBecome the go-to person for end-to-end data handling, management, and analytics processes. /p /lilipLead your team in creating the pipeline for Data management, data visualization, and analytics products, including automated services, and APIs. /p /lilipWorking with Data Scientists to take data throughout its lifecycle - acquisition, exploration, data cleaning, integration, analysis, interpretation, and visualization. /p /lilipBecome part of a fast-growing international and diverse team /p /li /ulh3What you will do /h3ullipPerform data analysis in the field of Growth Revenue Management, Marketing Analytics, CLM/CRM Analytics and/or Risk Analytics. /p /lilipConduct analyses in typical analytical tools ranging from SAS, SPSS, Eviews, R, Python, SQL, Teradata, Hadoop, Access, Excel, etc. /p /lilipCommunicate analyses via compelling presentations. /p /lilipSolve problems, disaggregate issues, develop hypotheses and develop actionable recommendations from data and analysis /p /lilipPrepare and facilitating workshops /p /lilipManage stakeholders and communicating with executives /p /lilipCoach and mentor team members /p /li /ulh3What you’ll bring /h3ullip3–5 years of professional experience in the analytics domain. /p /lilipAdvanced degree in a quantitative discipline (e.g., Mathematics, Computer Science, Programming, or related field). /p /lilipStrong analytical mindset with the ability to break down complex problems, formulate hypotheses, and derive actionable recommendations from data analysis. /p /lilipStrong technical expertise in data analysis, statistics, and programming, with proficiency in Python, Hadoop, SQL, and/or R. /p /lilipHands-on experience with Python data libraries and tools such as Jupyter, Pandas, Scikit-Learn, and Matplotlib. /p /lilipAbility to communicate effectively using the language of statistics, finance, and economics is a plus. /p /lilipFluent in English and Spanish (written and spoken). /p /li /ulpAt Metyis, we are driven by curiosity and collaboration. We value diversity, equity, inclusion, and belonging (DEIB) in all its forms as it makes us stronger as an organisation and promotes creativity and innovation. We welcome all talents and are committed to creating a workplace where every employee can make a meaningful impact and grow. /p /p #J-18808-Ljbffr

ppDesde AMA, la Mutua de los Profesionales Sanitarios, estamos buscando un Actuario de Vida y Solvencia II, para incorporar a nuestro equipo. ¿Tiene su CV preparado? Si es así y confía en que este es el puesto ideal para usted, asegúrese de enviar su solicitud lo antes posible. Los requisitos para el puesto : Licenciatura o Máster en Ciencias Actuariales y Financieras. Experiencia de al menos 2/3 años en Compañía Aseguradora y/o Consultoría. Conocimientos de productos de Vida Riesgo y Solvencia. Valorable conocimiento de herramientas como Prophet o RAFM. Buen manejo de hojas de cálculo, herramientas de bases de datos y estadísticas. Valorable conocimiento de SAS. Perfil multidisciplinar. Capacidad analítica. Capacidad de trabajo en equipo. Funciones: Cálculo de la Mejor Estimación de las Provisiones Técnicas bajo Solvencia II. Tarificación de productos de vida. Elaboración de informes de siniestralidad. Cálculo de provisiones contables y análisis de suficiencia. Análisis de nuevo negocio. Cálculo de la participación en beneficios. Te ofrecemos : Incorporación con contrato indefinido a empresa de referencia del sector. salario competitivo. grandes beneficios sociales. Formación continua. xbhjioe Flexibilidad horaria. Si eres esa persona, te estamos esperando para incorporarte a este Equipo!! /p /p #J-18808-Ljbffr

ppPivotal is excited to expand our team and we are looking for an experienced, highly motivated Clinical Data Scientist — AI Automation who shares our vision of providing clinical research excellence through the intelligent use of technology. /ppJoining Pivotal means becoming a member of one of the leading full‑service contract research organizations in Europe, with a very solid reputation. This role promises direct client experience, career growth, and professional development within a scientific and data‑driven company. You'll have the opportunity to work across a wide variety of therapeutic areas while actively shaping how AI transforms clinical research from the inside. /ph3Why Pivotal: /h3ulliWe are passionate and fully committed to medical science while leveraging cutting‑edge technology, including AI, to make a positive impact /liliWe provide an exceptional experience. We take care of our employees, ensuring everyone receives permanent mentoring, training, and a push to always take one step further, as well as international experience that will accompany you throughout your career /liliWe are continuously building our company, bringing together diversity of thoughts, backgrounds, cultures, and perspectives to create a place where everyone feels like they belong /li /ulh3Your responsibilities will include: /h3pYou will operate at the crossroads of clinical data science and AI engineering, applying advanced analytical and automation skills to accelerate and improve clinical research, including: /pulliAnalysing and interpreting complex clinical trial datasets to generate meaningful insights, identify trends, and support evidence‑based decision‑making across therapeutic areas /liliBuilding, testing, and deploying AI agents that autonomously handle repetitive clinical research workflows — including data monitoring, anomaly flagging, automated Python‑based report generation, and stakeholder notifications /liliLeveraging AI‑assisted development tools and publicly available LLMs to design, build, and iterate on analytical pipelines and automation solutions with speed and precision /liliDesigning and implementing predictive models and machine learning algorithms using frameworks such as scikit‑learn and TensorFlow to anticipate study risks and detect data quality issues proactively /liliDeveloping interactive visualizations, dashboards, and automated Python‑based reports to communicate findings clearly and consistently to both scientific and non‑technical stakeholders /liliEnsuring all AI‑powered solutions comply with applicable regulatory frameworks including GCP, 21 CFR Part 11, and GDPR /liliApplying ethical AI principles in a regulated clinical context, maintaining data governance, auditability, and patient data integrity at every stage /liliCollaborating with data architects, software engineers, biostatisticians, and product development teams to integrate AI solutions into existing clinical research infrastructure /liliSupporting study committee activities by providing timely, rigorous analytical outputs /liliStaying current with advances in AI, agentic systems, and data science methodologies and actively driving their adoption within Pivotal /liliPerforming other assigned duties as needed /li /ulh3Required profile: /h3ulliUniversity degree in Math, Physics, Data Science, Statistics, or a related field /lili4+ years of experience in clinical data science or related roles at a CRO or pharmaceutical company /liliUnderstanding of ICH/GCP guidelines, 21 CFR Part 11, and applicable data privacy regulations. /liliDemonstrated hands‑on experience building AI‑powered workflows, automation pipelines, or agentic systems in a clinical or scientific context /liliFamiliarity with publicly available LLMs, AI agent and orchestration frameworks (e.g., LangGraph), LLM observability and evaluation tools (e.g., LangSmith, LangFuse), and version control practices (Git) /li /ulh3Skills: /h3ulliStrong analytical thinking and ability to translate complex clinical data into actionable insights and scalable automated solutions /liliProficiency in Python for data analysis, automated reporting, and AI agent development; working knowledge of R, SQL, SAS, and data visualization tools /liliSolid understanding of ML frameworks (scikit‑learn, TensorFlow, or similar) for predictive modeling in regulated environments /liliHands‑on experience with modern LLM application stacks — including agent frameworks like LangGraph and observability/evaluation platforms such as LangSmith and LangFuse — to build, monitor, and iteratively improve production‑grade AI workflows /liliDeep commitment to ethical AI, data governance, and regulatory compliance in clinical research /liliGenuine drive to build and innovate, not just adopt existing tools /liliFluency in English (spoken and written) /liliEffective communication, collaborative mindset, and ability to work across multidisciplinary teams /li /ulh3What You Can Expect: /h3ulliA first‑of‑its‑kind role with real ownership — you won't be maintaining legacy processes, you'll be building new ones /liliCareer growth resources and flexible work schedules /liliTraining to enhance both therapeutic knowledge and cutting‑edge AI and data science tool proficiency /liliA forward‑thinking environment where your work directly shapes the future of clinical research at Pivotal /liliExposure to dynamic, international work environments and a wide variety of therapeutic areas /li /ulh3Commitment to Equal Opportunity: /h3pAt Pivotal, we believe that diversity and inclusion are essential to the success of our team. We are committed to providing equal employment opportunities to all candidates, regardless of race, gender, sexual orientation, disability, or any other characteristic. /p /p #J-18808-Ljbffr

pPsi-Cro is seeking a Biostatistics Project Lead to contribute to statistical activities in global clinical trials and to work with international teams of statisticians, SAS programmers and data managers. /ppYou will develop and review study protocols, SAPs and ADaM datasets, conduct analyses (interim, final, PK) and lead teams on project level, ensuring quality and regulatory compliance. MSc in Statistics and fluent English are required. /p #J-18808-Ljbffr

Experteer Overview In this role you will guide clients through uncertainty, helping them strengthen resilience and grow. You’ll work with global clients across diverse industries in Core Risk or Risk Analytical functions, using data-driven methods to quantify risk and inform strategy. You operate in a high-performance culture with strong mentorship and learning, shaping practical solutions and enterprise risk capabilities. This is an opportunity to develop leadership through challenging engagements and impactful client work. Compensaciones / Beneficios • Guide clients through uncertainty to strengthen governance, processes, and resilience. • Identify and address immediate risks and gaps across risk management dimensions. • Develop and embed enterprise risk management capabilities for sustainable growth. • Leverage data-driven scenario planning, stress-testing, and advanced modeling to quantify risk exposures. • Translate insights into actionable strategies and institutionalize resilience for clients. • Collaborate with cross-functional teams to deliver risk solutions in Core Risk or Risk Analytical functions. Responsabilidades • Master's degree • 1+ years of experience in risk management and/or risk quantitative analysis/modelling • Experience in consultancy with risk focus or related banking/regulatory domains • Exceptional conceptual problem-solving and quantitative modeling skills • Programming experience in Python, R, or similar; knowledge of SQL/NoSQL/ Matlab/SAS is advantageous • Familiarity with ML/AI (NLP, deep learning, anomaly detection) and GenAI/LLM is a plus • Willingness to travel • Fluency in English and local office language(s) to communicate complex ideas Requisitos principales • competitive salary • comprehensive benefits package • global client exposure • mentorship and structured learning • development-focused culture • apprenticeship and coaching

Psi-Cro is seeking a Biostatistics Project Lead to contribute to statistical activities in global clinical trials and to work with international teams of statisticians, SAS programmers and data managers. You will develop and review study protocols, SAPs and ADa M datasets, conduct analyses (interim, final, PK) and lead teams on project level, ensuring quality and regulatory compliance. MSc in Statistics and fluent English are required. #J-18808-Ljbffr

ppProfessional | Permanent | Full-time | Hybrid If you’re passionate about changing lives for the better, this is the opportunity you’ve been waiting for. In bResearch Development /b, we’re continuously exploring innovative new treatment options to make a stronger, more positive impact on the lives of the patients we serve. You’ll work with talented colleagues in a state‑of‑the‑art Research Development environment, developing innovative medicines that change the life of patients for the better and help us make progress towards our vision of a world free of pain. Join us today, and discover the difference you can make. /p h3What The Job Looks Like /h3 ul liSet the strategic direction to build the statistical and clinical unbiased evidence for all clinical phases (I‑III), regulatory submissions, market access and life cycle management. /li liContribute in collaboration with all scientists in DEV to design the trials for Phase I‑III (PoC, late development and life cycle management), including the definition of Go/No Go criteria ensuring best possible decision /li liOversee and support creation of the statistical analysis plans defining the most‑advanced and appropriate statistics for the analyses of the trial data, integrated data, Real World Data and omics data /li liInterpret the results of the analyses and communicate them clearly with the most advanced and accurate visualization tools. /li liReach out to the highest quality outsourcing providers and academia partners, communicate clearly and keep oversight according to regulations standards /li liBuild strong relationships with commercial partners to support clinical development activities as needed in a fully outsourced and virtual working model /li /ul h3What You'll Bring To The Table /h3 ul liPhD in biostatistics, statistics, mathematics or MSc from high‑ranked university, data scientist or equivalent /li liAt least 10 years of experience in the pharmaceutical industry /li liHands on experience in programming the analyses of data and data mining in SAS and R and other software /li liProfound knowledge of most advanced statistics, probability and mathematics /li liExperience in designing, reviewing and providing input into SOW for external service providers in collaboration with other functions /li liBe able to communicate high complex biostatistical concepts to non‑statisticians in an understandable way /li liFluent business English language skills in speaking and writing, additional language skills beneficial /li /ul pb"Become part of our multicultural and interdisciplinary team and join us on an exciting journey towards a World Free of Pain" /b /p pHeiko Hagedorn, the Hiring Manager /p /p #J-18808-Ljbffr

Roche is seeking a Lead System Architect (LSA) for the Platform Architect role to define the enterprise ECS, govern the DPA ecosystem, and ensure reusable, scalable automation solutions. You will serve as the primary technical consultant to the Product Owner and stakeholders, shaping blueprints and architecture across complex Pega implementations. You will mentor SSAs and SAs, drive Dev Ops adoption, and partner with the business to align the DPA roadmap with technical feasibility and #J-18808-Ljbffr

Syneos Health, Inc. is looking for a Sr/Principal Statistician based in Madrid, Spain. This role involves providing statistical support across clinical projects, including the development of Statistical Analysis Plans and coordination of biostatistics activities. The ideal candidate should have a Ph D/MS in statistics or a related field with at least 3 years of experience in the pharmaceutical industry, along with proficiency in SAS and R. This position may require minimal travel and offers the opportunity to mentor junior staff. #J-18808-Ljbffr

ppAt Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. /p h3The Position /h3 pbData Scientist Submission Data and Content Generation Reuse (AIDCG) - Pharma RD /b /p pAre you passionate about leveraging cutting‑edge artificial intelligence and data science to transform patient care? As a Data Scientist, you will play a pivotal role in leading, developing, and deploying innovative, data‑driven solutions to solve complex business problems. You will balance hands‑on technical execution with strategic content leadership, building state‑of‑the‑art AI capabilities that directly accelerate healthcare innovation. /p pAt Roche, we offer a bhybrid work model /b that combines flexibility with in‑person collaboration. For now, we require our employees to be in our offices on average two days per week. The specific office days may vary depending on business needs, such as workshops, conferences, town halls, team meetings, and other collaborative events. /p h3Description Of The Area /h3 pThe Clinical Submission Data and Content Generation Reuse function focuses on modernizing the creation and management of clinical data and regulatory submission assets (data and content). It develops and deploys platforms for structured content management, enabling the reuse of approved components across documents. This group also pioneers the use of agentic AI to assist in generating, reviewing, and assembling complex submission assets (data and content), aiming to improve quality and reduce authoring timelines. /p h3The Opportunity /h3 ul liEnd-to-End Solution Ownership: Lead, develop, and deploy data-driven solutions and predictive models from inception to deployment to tackle complex business challenges /li liAgentic AI Development: Build specialized AI agents and bespoke multi-agent workflows in a highly regulated GxP environment to support Analytical Data Scientists across the clinical data lifecycle /li liIndependent Problem Solving: Identify analytical opportunities independently and solve complex data problems, ensuring model accuracy and validation with minimal supervision /li liCross-Functional Collaboration: Engage directly with business units to understand their data requirements and translate analytical findings into actionable insights for both technical and non-technical stakeholders /li liStrategic Project Leadership: Drive medium-sized data science projects that directly influence key business decisions and align with broader organizational strategies /li liData Modeling Optimization: Work with large, complex datasets to build new predictive models from scratch and optimize existing algorithms for maximum performance /li liTechnical Roadmap Guidance: Frequently contribute to the team’s technical roadmap, balancing hands-on AI/ML development with strategic technical leadership /li liProcess Automation: Develop innovative tools, such as proactive coding debuggers that parse verbose logs and automatically propose code/configuration fixes for complex clinical programming /li /ul h3Who You Are /h3 ul liEducation Experience: Master’s or Bachelor’s degree in Data Science, Computer Science, Statistics, or a related quantitative field, paired with a minimum of 5+ years of professional experience in data science, predictive modeling, and end-to-end deployment /li liProject Delivery Ownership: Proven track record of independently identifying analytical opportunities, leading medium-sized data science projects, and delivering solutions that drive business outcomes /li liProgramming Proficiency: Advanced proficiency in Python (for AI/ML backends and agent logic) and R (focused on clinical statistical programming and NextGen toolkits like Admiral); familiarity with SAS is preferred /li liGenerative AI Agent Frameworks: Hands‑on experience building multi‑agent architectures using LangChain, LangGraph, AWS AgentCore, and Model Context Protocol (MCP) servers /li liAdvanced RAG Expertise: In‑depth knowledge of LLMOps and advanced Retrieval‑Augmented Generation (RAG) methodologies, including chunking strategies, embeddings, and GraphRAG /li liStatistical Modeling Visualization: Strong foundational expertise in advanced statistical methods, machine learning algorithms, and data visualization techniques to support complex data exploration /li liCommunication Collaboration: Exceptional communication and interpersonal skills, with a demonstrated ability to convey complex technical concepts clearly to non-technical partners /li /ul h3Compensation Benefits /h3 pThe expected salary range for this position, based on the primary location of Warsaw Grafit is 170,100.00 PLN - 315,900.00 PLN. Final compensation will be determined by a number of factors, including your skills, experience, qualifications, and location. In addition to base pay, this role may be eligible for a discretionary annual bonus with a target of 15% subject to both individual and company performance. /p pThis position also offers an attractive benefits package. /p pLearn more about how we reward our employees at Roche. /p pThis job is posted in multiple locations. If you're applying for the role in an alternative location where pay transparency regulations apply, the Talent Acquisition Partner will share the local pay information with you ahead of any business interview. /p bRoche is an Equal Opportunity Employer. /b /p #J-18808-Ljbffr

Sr/Principal Statistician (Sponsor-dedicated) Many possible locations (EMEA) Updated: TodayLocation: Madrid, SpainJob ID: 25109875-OTHLOC-3529-2 DMAD-2 DR Sr/Principal Statistician (Sponsor-dedicated) Many possible locations (EMEA) As a biostatistician with Syneos Health, you will provide support across all assigned statistical tasks throughout the lifecycle of clinical projects. Your responsibilities include developing and reviewing Statistical Analysis Plans (SAPs), coordinating activities of the biostatistics and statistical programming team, creating programming specifications, and ensuring compliance with SOPs and regulatory guidelines. You may also provide statistical programming support, participate in data safety monitoring and regulatory meetings, and mentor junior staff. Supports scientific design of the clinical studies and prepares Statistical Analysis Plans (SAPs) including mock-up displays for tables, listings, and figures. Coordinates activities of other biostatistics and statistical programming personnel to ensure timely, high-quality output and provides independent review of project work. Creates or reviews programming specifications for analysis datasets, tables, listings, and figures. Reviews SAS annotated case report forms (CRFs), database design, and other study documentation to ensure protocol criteria are met. Conducts verification and quality control of project deliverables, ensuring outputs align with SAP and specifications. Serves as biostatistics representative on project teams and interfaces with other departmental representatives. Manages scheduling and time constraints across multiple projects, sets priorities, adapts to timeline changes, and communicates challenges to biostatistics management. Monitors progress on study activities against milestones and ensures deliverables are met, escalating out-of-scope tasks to management. Provides statistical programming support as required. Participates in Data Safety Monitoring Board and/or Data Monitoring Committee activities, as needed. Leads integrated analyses, attends regulatory agency meetings, and responds to questions regarding statistical analysis results on behalf of the sponsor. Follows applicable SOPs, WI, and regulatory guidelines such as ICH. Maintains comprehensive, up-to-date project documentation and verification/quality control records, ensuring inspection readiness. Displays teamwork, assists with projects, and supports business development activities such as proposals, budgets, and sponsor bid defense meetings. Coaches and mentors other biostatistics staff. Performs additional related duties as assigned. Travel may be required minimally. Summary Ph D/MS in statistics or a related discipline with at least 3 years of pharmaceutical experience. Strong knowledge of advanced statistical concepts and methods. Proficiency in SAS or R, and experience with meta-analyses and late-phase clinical trials is highly preferred. Equal Opportunity Employer The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. #J-18808-Ljbffr

pGrant Thornton España busca un/a profesional para colaborar en proyectos de consultoría en España e internacionalmente, especialmente en seguros de vida y no vida. Participará en desafíos regulatorios, cálculos de valor y desarrollo de modelos actuariales, con enfoque en Solvencia II e IFRS17. /ppSe valorará experiencia de 2 a 4 años, dominio de Office y conocimientos de herramientas de modelización actuarial, además de habilidades de programación (Visual Basic, SAS, C++). /p #J-18808-Ljbffr

pIQVIA is seeking a motivated HTA Analyst-Programmer in Madrid to contribute to health technology assessments and market access activities in Germany. The ideal candidate will have a Master’s degree or PhD in biostatistics or related fields and at least 2 years of experience in advanced SAS programming. /ppThe role requires strong analytical skills and fluency in German and English, as the candidate will collaborate with cross-functional teams to ensure quality in outcomes and programming of statistical analyses. /p #J-18808-Ljbffr

ph3Sr/Principal Statistician (Sponsor-dedicated) Many possible locations (EMEA) /h3 pbUpdated: /b Todaybr/bLocation: /b Madrid, Spainbr/bJob ID: /b -OTHLOC-3529-2DMAD-2DR /p pSr/Principal Statistician (Sponsor-dedicated) Many possible locations (EMEA) /p pAs a biostatistician with Syneos Health, you will provide support across all assigned statistical tasks throughout the lifecycle of clinical projects. Your responsibilities include developing and reviewing Statistical Analysis Plans (SAPs), coordinating activities of the biostatistics and statistical programming team, creating programming specifications, and ensuring compliance with SOPs and regulatory guidelines. You may also provide statistical programming support, participate in data safety monitoring and regulatory meetings, and mentor junior staff. /p ul liSupports scientific design of the clinical studies and prepares Statistical Analysis Plans (SAPs) including mock-up displays for tables, listings, and figures. /li liCoordinates activities of other biostatistics and statistical programming personnel to ensure timely, high-quality output and provides independent review of project work. /li liCreates or reviews programming specifications for analysis datasets, tables, listings, and figures. /li liReviews SAS annotated case report forms (CRFs), database design, and other study documentation to ensure protocol criteria are met. /li liConducts verification and quality control of project deliverables, ensuring outputs align with SAP and specifications. /li liServes as biostatistics representative on project teams and interfaces with other departmental representatives. /li liManages scheduling and time constraints across multiple projects, sets priorities, adapts to timeline changes, and communicates challenges to biostatistics management. /li liMonitors progress on study activities against milestones and ensures deliverables are met, escalating out-of-scope tasks to management. /li liProvides statistical programming support as required. /li liParticipates in Data Safety Monitoring Board and/or Data Monitoring Committee activities, as needed. /li liLeads integrated analyses, attends regulatory agency meetings, and responds to questions regarding statistical analysis results on behalf of the sponsor. /li liFollows applicable SOPs, WI, and regulatory guidelines such as ICH. /li liMaintains comprehensive, up-to-date project documentation and verification/quality control records, ensuring inspection readiness. /li liDisplays teamwork, assists with projects, and supports business development activities such as proposals, budgets, and sponsor bid defense meetings. /li liCoaches and mentors other biostatistics staff. /li liPerforms additional related duties as assigned. /li liTravel may be required minimally. /li /ul pbSummary /b /p pPhD/MS in statistics or a related discipline with at least 3 years of pharmaceutical experience. Strong knowledge of advanced statistical concepts and methods. Proficiency in SAS or R, and experience with meta-analyses and late-phase clinical trials is highly preferred. /p pbEqual Opportunity Employer /b /p pThe Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. /p /p #J-18808-Ljbffr

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position As the Lead System Architect (LSA) - Platform Architect, you will serve as the highest technical authority for the Pega Platform within the Workflow Automation team. In this strategic role, you define the enterprise class structure, lead the technical governance of the Digital Process Automation (DPA) ecosystem, and ensure all automation solutions are built for maximum reuse, scalability, and performance. You act as the primary technical consultant for the Product Owner and business stakeholders, transforming high-level business visions into robust, future-proof architectural blueprints. Define and enforce the Pega Enterprise Class Structure (ECS) and foundational architectural layers. Your Responsibilities Lead technical reviews for high-complexity initiatives and ensure strict adherence to development guardrails Solve complex technical challenges and architectural ambiguities, conducting feasibility studies and performance impact assessments for enterprise-wide integrations Act as the ultimate technical mentor for Senior System Architects (SSAs) and System Architects (SAs), fostering a culture of continuous learning and engineering excellence Partner closely with the Product Owner to influence the DPA roadmap from a technical feasibility and sustainability perspective Oversee system health, security compliance, and performance tuning using diagnostic tools Drive the implementation of modern Dev Ops, CI/CD, and automated testing strategies for the platform Who You Are You are a visionary technical leader who balances immediate delivery needs with long-term platform stability. You possess a passion for challenging the status quo and driving continuous innovation in Digital Process Automation You bring a minimum of 8–12 years in software engineering, with at least 5–7 years dedicated specifically to Pega platform architecture Certification: A valid Pega Lead System Architect (LSA) certification is a mandatory requirement for this role Track Record: You have proven experience leading the technical architecture for large-scale, multi-stream Pega implementations in a global environment Technical Mastery: Deep expertise in Pega Infinity (8.X/24.X) Case Management, Dev Ops (Deployment Manager), and Security models Integration & Performance: Expert knowledge of microservices, REST/SOAP, OAuth, and Kafka integrations, alongside advanced proficiency in diagnostic tools and database optimization Infrastructure: Strong understanding of cloud-native Pega deployments (AWS/Azure) and containerization Communication: Excellent communication and stakeholder management skills, with a proven ability to influence senior technical leaders and navigate complex team dynamics At Roche, we aim high to deliver life-changing healthcare solutions. If you’re ready to make a meaningful impact on patients and healthcare systems worldwide, this is the place for you. Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer. #J-18808-Ljbffr