IQVIA

Territory Business Manager Location: North Yorkshire, North East, North Cumbria Do you want to join a company that nurtures its employees and advocates for an employee work-life balance? Do you have excellent sales experience and wish to join a company that has led the way in the development, manufacture, and marketing of innovative dermatology products for many years? We are delighted to announce we have an excellent new Medical Sales Representative role with a client dedicated to driving skin care forward! Our client is seeking an experienced sales representative who will be responsible increasing sales and market share for its innovative and already-loved product. They are looking for someone with: Experience selling to the NHS, Dermatologists, Primary and Secondary Care, Tissue Viability NursesExperience in GP sales, specifically relationship building and excellent local customer networksExperience working to KPIsExcellent analyticalUniversity degree is preferred but not essentialEnterprising and enthusiastic self-starter, adaptable to changeYou will be responsible for: Winning and retaining business on the local health formularies in the territory.Gaining agreement to prescribe or recommend our products by influencing prescribing habits of relevant HCPsGrowing market share in all relevant heath economiesDeveloping Key Opinion Leaders and leveraging their support to gain new advocates (for example via local evening and speaker meetingsWorking in partnership with your territory Pharmacy Sales RepresentativeAttending trade shows and conferences.If you are looking for an exciting new challenge with a company that genuinely believes in nurturing and supporting its employees to make a difference in the health care industry, this IS the job for you! In return, your contributions will be rewarded with: Excellent salary and Bonus Competitive pension scheme, Group Life Cover, Group Income Protection27 Day’s annual leave + bank holidaysGenerous Car allowancePrivate healthcare for you AND your familyOnline wellbeing support available 24 hours a day, 7 days a week, 365 days a year Please note: Sponsorship is not available for this opportunity. #LI-DNI #LI-CES #LI-WB1 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Title: Medical Data Review Manager - RheumatologyLocation: Argentina Job Overview:As a Medical Data Review Manager specializing in Rheumatology you will oversee the review and management of clinical data to ensure accuracy consistency and compliance with regulatory standards. Your role will involve collaborating with cross-functional teams to support the development and execution of clinical trials in the field of rheumatology. You will be responsible for ensuring high-quality data deliverables and providing expert guidance on data management processes. IQVIA Overview:IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. Our work accelerates the development and commercialization of medical treatments that improve patient outcomes and population health worldwide. With a multidisciplinary team of 88000+ experts spanning data science commercialization regulatory and technology IQVIA empowers its consultants to translate the world’s most pressing healthcare challenges into actionable strategies that speed new therapies to market. Responsibilities: Oversee the review and management of clinical data for rheumatology studies.Ensure data accuracy consistency and compliance with regulatory standards.Collaborate with cross-functional teams to support clinical trial development and execution.Provide expert guidance on data management processes and best practices.Develop and implement data review plans and strategies.Monitor data quality and address any discrepancies or issues.Participate in audits and inspections to ensure compliance with quality standards.Qualifications: Bachelor's Degree in a healthcare or scientific discipline.Proven experience in clinical data management preferably in rheumatology.Strong understanding of regulatory and quality standards in clinical data management.Excellent leadership communication and interpersonal skills.Ability to manage multiple tasks and projects simultaneously.Strong analytical and problem-solving skills.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Location: Field based, UK An exciting opportunity for a commercially driven Key Account Manager to lead and grow pharmacy accounts within the FMCG Health and Beauty sector. You will deliver profitable growth, build strong customer relationships and coach Pharmacy Business Managers to strengthen account performance across the division. Key responsibilitiesDeliver sales growth in line with budgets and forecastsCreate and execute strategic account plansBuild multi level relationships with key stakeholdersCoach Pharmacy Business Managers to drive performanceNegotiate pricing, promotions and budgets to maximise ROIAnalyse sales data and provide accurate forecastsIdentify new business opportunities within pharmacy channelsMaintain CRM records and ensure regulatory complianceAbout youProven Key Account Management experience in FMCG, ideally Health and Beauty or pharmacyStrong track record of delivering profitable growth in B2B environmentsCommercially minded with excellent analytical and negotiation skillsConfident communicator, comfortable engaging senior stakeholdersProficient in Excel, PowerPoint and CRM systemsPassion for developing others and driving resultsWhy joinHigh impact, autonomous role in a growing sectorCareer development and progression opportunitiesCollaborative and inclusive team culturePlease note this role does not sponsor visa's.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Position Title: Mass Market RepresentativeLocation: BotswanaIndustry: Pharmaceutical / FMCG / HealthcareEmployment Type: Contractor A leading Consumer Healthcare company is seeking a results-driven Mass Market Representative with proven experience in the retail pharmacy space. This role is ideal for a candidate with strong field execution skills, a passion for consumer health, and the ability to drive visibility and availability of products across mass market channels. Key Responsibilities: Visit channel-specific outlets regularly to ensure product availability in collaboration with distributor teams.Deploy company Point-of-Sale Materials (POSM) across assigned outlets.Oversee and support the execution of company activations within the designated channel.Submit weekly, monthly, and quarterly reports on sales, stock levels, and market activities.Gather and report market insights and competitor activities to inform strategy.Qualifications & Requirements: Minimum of a diploma in Sales, Marketing, or a related field; a degree is an advantage.At least 3 years’ experience in the Pharmacy FMCG environment.Previous experience working in retail pharmacy is essential.Valid driver’s license and access to a reliable vehicle.Must be a resident of the country in scope and legally able to work there.This is a great opportunity to be part of a dynamic team focused on delivering impactful consumer healthcare solutions. You’ll play a key role in driving brand visibility, market execution, and retail excellence. #LI-DNP #LI-CES  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

Buscamos un/a Desarrollador/a Full Stack apasionado/a por la tecnología y el desarrollo de soluciones escalables para unirse a nuestro equipo. Esta posición será responsable de diseñar, desarrollar e implementar aplicaciones web modernas de extremo a extremo, trabajando tanto en el desarrollo backend como frontend y participando en la arquitectura, despliegue y evolución de soluciones en la nube. La persona ideal cuenta con experiencia construyendo APIs robustas con Python y FastAPI, desarrollando interfaces dinámicas con React o Next.js y desplegando aplicaciones en entornos AWS. Responsabilidades PrincipalesDiseñar, desarrollar y mantener aplicaciones web full stack escalables y de alto rendimiento.Desarrollar y consumir APIs REST utilizando Python y FastAPI.Crear interfaces de usuario modernas, intuitivas y responsivas utilizando React.js y/o Next.js.Diseñar, optimizar y administrar bases de datos relacionales y NoSQL, incluyendo PostgreSQL y MongoDB.Integrar servicios de terceros y desarrollar soluciones orientadas a escalabilidad y mantenibilidad.Implementar, monitorear y administrar aplicaciones en AWS.Desarrollar pruebas unitarias e integraciones para asegurar la calidad del software.Garantizar el rendimiento, la seguridad y la disponibilidad de las aplicaciones.Colaborar con equipos multidisciplinarios de Producto, Diseño, QA y DevOps bajo metodologías ágiles.Participar en revisiones de código, documentación técnica y definición de mejores prácticas de desarrollo.RequisitosExperiencia y Conocimientos TécnicosMás de 3 años de experiencia como Desarrollador/a Full Stack.Dominio de Python y experiencia desarrollando APIs con FastAPI.Experiencia sólida en React.js y/o Next.js.Conocimientos avanzados de JavaScript/TypeScript, HTML5 y CSS3.Experiencia trabajando con PostgreSQL y MongoDB.Experiencia desplegando y administrando soluciones en AWS, incluyendo servicios como:EC2LambdaS3RDSECSECRCloudWatchIAMAPI GatewayExperiencia con Docker y tecnologías de contenerización.Manejo de Git y flujos de trabajo colaborativos en equipos de desarrollo.Conocimientos de autenticación y seguridad de aplicaciones (JWT, OAuth2).Experiencia trabajando bajo metodologías ágiles como Scrum o Kanban.Requisitos DeseablesExperiencia implementando procesos de CI/CD con GitHub Actions, GitLab CI o AWS CodePipeline.Conocimientos de Terraform o CloudFormation para infraestructura como código.Experiencia con Redis, Celery o arquitecturas de procesamiento asíncrono.Familiaridad con Kubernetes o Amazon EKS.Conocimientos de GraphQL.Experiencia desarrollando pruebas automatizadas con Pytest, Jest o Playwright.Competencias BlandasPensamiento analítico y orientación a la resolución de problemas.Capacidad para trabajar de manera autónoma y colaborativa.Comunicación efectiva con equipos técnicos y no técnicos.Proactividad y mentalidad de mejora continua.Atención al detalle y compromiso con la calidad del código.Capacidad para adaptarse a entornos dinámicos y proyectos de alta complejidad.Stack TecnológicoBackend: Python, FastAPIFrontend: React.js, Next.js, TypeScriptBases de Datos: PostgreSQL, MongoDBCloud: AWS (EC2, Lambda, S3, RDS, ECS, ECR, CloudWatch, IAM, API Gateway)DevOps: Docker, Git, CI/CD, GitHub ActionsMetodologías: Scrum, Kanban ¿Qué Buscamos?Buscamos una persona con pasión por construir productos de calidad, que disfrute resolver problemas complejos y trabajar con tecnologías modernas. Valoramos perfiles con iniciativa, orientación a resultados y capacidad para colaborar con equipos multidisciplinarios en el desarrollo de soluciones innovadoras y escalables. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

En IQVIA buscamos un Data Analyst apasionado por los datos y la analítica para transformar información en insights accionables que apoyen la toma de decisiones del negocio. La persona seleccionada trabajará con grandes volúmenes de datos, construirá reportes e indicadores clave, y contribuirá a mejorar la calidad y eficiencia de nuestros procesos analíticos. Responsabilidades PrincipalesExtraer, transformar y analizar datos provenientes de múltiples fuentes utilizando SQL. Desarrollar dashboards, reportes y visualizaciones en herramientas de Business Intelligence como Power BI o Tableau. Automatizar consultas y procesos de análisis para optimizar la eficiencia operativa. Identificar patrones, tendencias y oportunidades a partir de los datos. Participar en procesos de integración y transformación de datos (ETL). Garantizar la calidad, consistencia e integridad de los datos dentro de los procesos analíticos. Documentar metodologías, consultas y procesos para asegurar la trazabilidad y escalabilidad de las soluciones desarrolladas. Colaborar con equipos multidisciplinarios para traducir necesidades de negocio en soluciones basadas en datos. RequisitosExperiencia y Conocimientos Técnicos2 años de experiencia en análisis de datos, inteligencia de negocios o roles similares. Dominio avanzado de SQL para extracción, transformación y análisis de datos. Experiencia práctica utilizando Python para análisis y automatización de procesos. Experiencia creando dashboards y reportes en al menos una herramienta de BI (Power BI, Tableau o similar). Manejo avanzado de Microsoft Excel (tablas dinámicas, fórmulas avanzadas, análisis de datos). Conocimiento de procesos ETL o herramientas de integración de datos. Capacidad para trabajar con grandes volúmenes de información y múltiples fuentes de datos. Competencias BlandasPensamiento analítico y orientación a la resolución de problemas. Alta atención al detalle y enfoque en la calidad. Capacidad para trabajar de manera colaborativa en equipos multidisciplinarios. Proactividad, curiosidad y aprendizaje continuo. Habilidades de comunicación para presentar hallazgos de manera clara a diferentes audiencias. ¿Qué buscamos?Una persona apasionada por los datos, con mentalidad analítica y capacidad para convertir información compleja en recomendaciones de valor para el negocio. Buscamos alguien con iniciativa, orientación a resultados y un fuerte interés en mantenerse actualizado sobre las últimas tendencias y mejores prácticas en analítica de datos. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewWorks in the Canada Custom Data Extracts (CDE) to deliver the work requests in time without any errors. Assists with the design/development of software solutions requiring general domain knowledge and limited business expertise.Troubleshoots code issues and continuously evolves IQVIA's platforms to meet user requirements/needs. Essential Functions• Assists with the design/development of software solutions requiring general domain knowledge and limited business expertise.• Works at all layers of the application stack including front-end user interface and backend development.• Troubleshoots code issues and continuously evolves IQVIA's platforms to meet user requirements/needs.• Reviews functional specifications and other validation deliverables as assigned.• Develops a basic understanding of industry and IQVIA-specific quality standards.• Supports development projects based on specific instructions and with limited discretion.• Typically requires 1 year of prior relevant experience. Qualifications• Bachelor's Degree Computer Science, a related field, or equivalent experience Good skills in Oracle PL/SQLPreferred: Knowledge in Python and any BI tool (e.g. Power BI) IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewProvide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager. Essential Functions• Serve as a Data Operations Coordinator (DOC) for one protocol with less then 5 operations staff (excludes DE) or 15+ easy to moderately complex central laboratory studies, or serve in a leadership role in a specific data management task (e.g., coder, tester or database designer for technologies that don't require extensive programming expertise) with guidance.• May serve in the role of back-up to a DOC or DTL.• May conduct data review.• May write and resolve data clarifications.• May lead database audit team.• May develop and test databases and edit specifications.• May perform testing of programming.• May perform clinical data coding. Understand and comply with core operating procedures and working instructions. Meet objectives as assigned. Develop and maintain good communications and working relationships with CDM team." Qualifications• Bachelor's Degree Clinical, biological or mathematical sciences, or related field Req• Equivalent combination of education, training and experience in lieu of degree.• Medical terminology exposure. Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Medical terminology exposure. Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Essential Functions• Develops and delivers technology services through managed services project activities requiring general knowledge of IQVIA's products and technical expertise.• Responsible for identifying additional product/services opportunities for clients makes decisions within limited parameters under regular supervision.• Has broad understanding of quality standards and work requires minimal revision.• Assists in problem identification, system architecture definition, hardware/software specification and/or design, implementation, testing, client training and solution deployment.• Provides support on Service Requests using the incident management tool, CSM.• Coordinates the routing and handling of Requests For Change to the next level of support under regular supervision.• Escalates issues relating to product support or product operations to the next level of support.• Project management activities include interaction with company and client managers and cost/schedule monitoring. Qualifications• Bachelor's Degree Computer Science, a related field, or equivalent experience Req IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewResponsible for study build & design, edit specifications, system configurations and is accountable for associated study design components. This role will collaborate with various stakeholders- DTL, Programmer, Validation Team, vendors, statisticians, and client representatives. In addition to project deliveries, the role also would be responsible for the project financials from programming shared services perspective. Essential Functions• Interprets the study protocol.• Design and update the eCRF using third party or in house CDMS tools in alignment with industry standards like SDTM, CDASH as applicable.• Create and update Edit Specification Document.• Generate specifications for EDC build components (e.g., Rights and Roles, System Settings and Home Page)• Complete the Study Authorization Form and Trial Capacity Request Form (InForm)• Attend the Pre-Design Meeting, Online Screen Review Meeting, Unblinded Data review meeting.  Attend and present comments at the Internal Design Review Meeting.  May lead Online Screen Review Meeting.• Facilitate the internal Edit Specification Review Meeting and leads the discussions regarding the Edit Specification Document.• Design the database to collect LLRR data within the InForm database and ensure Rights and Roles document has appropriate access for Entry and Updates.• Communicate any project risks to the Data Team Lead, including the potential for missing a timeline in the Data Management Project Plan.• Escalate potential quality issues.• Ensure the completion and documentation of all project-specific training, as well as staying current with required Standard Operating Procedures.• Reviews build timelines and provide input as applicable.• Reviews QIP for own projects, identify out of scope activities if any and inform relevant parties.• Responsible for multiple study design projects at the same time.• Might be working on projects across multiple platforms.• Identify areas for process improvements on an ongoing basis. Actively take part and contribute towards process improvement initiatives as assigned besides providing suggestions for continuous improvement of processes.• All responsibilities are essential job functions unless noted as nonessential (N). Qualifications• Bachelor's Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology  Req• 2-4 years of relevant core Technical designer experience and total exp being 7+ yrs.   Req IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Required skills and experience:• 1/2+ years of experience working with Azure or AWS or any other major cloud platform technologies• Provisioning, operating, and maintaining systems running on Azure or AWS including deployment/teardown and automation support• Understanding of cloud platforms including IaaS & PaaS components, for example: Azure Virtual Machines/EC2 Instances, Storage Accounts/S3 buckets, Network Security Groups, vNets, VPCs, Azure App Services/AWS Lambda, Kubernetes basics etc• Exposure to scripting or automation tools (e.g., PowerShell, Python, Bash, Azure CLI, AWS CLI) is desirable• Understanding of Infrastructure as code (IaC) and CI/CD pipeline concepts – example: Terraform, Gitlab, ADO• Good practical experience with Windows and Linux operating systems, including administration tasks such as OS configuration, patching, user management, system monitoring, and troubleshooting• Knowledge of network (LAN, WAN, VPN) and web related protocols (e.g. TCP/IP, UDP, HTTP, HTTPS)• Exposure to monitoring tools such as Azure Monitor, Log Analytics, Application Insights or AWS CloudWatch is desirable• Understanding of backup and patching concepts in cloud environments• Awareness of security concepts such as RBAC, IAM roles, access provisioning and secure configurations• Good awareness of cloud platform capabilities and willingness to learn new features• Knowledge on installation, configuration, usage of CLI tools to manage cloud components is desirable• Experience with documentation and following operational runbooks is desirable• Good troubleshooting and analytical skills for cloud issues• Understanding of ITIL/ITSM processes including incident/request management. ServiceNow exposure is a bonus• Good to have: Awareness of AI concepts and their applicability in IT operations (e.g., automation, monitoring insights)• Prior experience in Life Sciences area is also a bonus. Other highly regulated industry experience will be considered also Education/certification:•    Degree level educated, preferably in science, maths or engineering areas.•    Azure or AWS Fundamentals level certification is preferred. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewProvide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager. Essential Functions• Serve as a Data Operations Coordinator (DOC) for one protocol with less then 5 operations staff (excludes DE) or 15+ easy to moderately complex central laboratory studies, or serve in a leadership role in a specific data management task (e.g., coder, tester or database designer for technologies that don't require extensive programming expertise) with guidance.• May serve in the role of back-up to a DOC or DTL.• May conduct data review.• May write and resolve data clarifications.• May lead database audit team.• May develop and test databases and edit specifications.• May perform testing of programming.• May perform clinical data coding. Understand and comply with core operating procedures and working instructions. Meet objectives as assigned. Develop and maintain good communications and working relationships with CDM team." Qualifications• Bachelor's Degree Clinical, biological or mathematical sciences, or related field Req• Equivalent combination of education, training and experience in lieu of degree.• Medical terminology exposure. Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Medical terminology exposure. Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewIndependently manage end-to-end delivery of data management services for single/multi-service projects, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products that meet customer needs. Provide leadership and vision to the team in the areas of project planning, execution, and close-out; financial management; communications; and milestone deliverables. May perform role of Data Team Lead (DTL), Program Lead, Customer Site Manager, and/or a leadership role in a specific CDM task (e.g. Subject Matter Expert (SME). Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where available, CDM guidance documents. Essential Functions• Client Management: Serve as primary point of contact for customer on data management deliverables• manage multiple large studies or program of studies (possibly global) Provide leadership and senior support to DTLs on multiple large global studies/programme of global studies Provide leadership and senior support to DTLs on multiple large global studies/programme of global studies.• Provide project management expertise working with customer data managers, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections, and provide technical expertise• Lead direct negotiations with customer, e.g., timelines, financial, process, resources.• Maintain strong customer relationships• Ensure open communications with customer and IQVIA management to independently manage and meet contractual obligations• Service Management:• Meet with Data Operations Coordinator (DOC) and/or Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables• provide training and development on data management expertise to junior team members• Establish strong communications with Data Operations team, functional leads, project managers and all other stake holders• Independently manage DM service delivery with comprehensive DM process and technical expertise in executing projects• Serve as the escalation point for unresolved data issues• independently work with client data managers, vendors, internal team members for resolution• Ensure appropriate resources are assigned to meet project deliverables• Create and/or review and sign-off on all data management plan (DMP) documents• Ensure service and quality meet agreed upon specifications per the DMP and contract/SOW• Implement proactive quality management plans across multiple projects/programmes/customer account. Manage service performance and provide leadership to identify root causes of issues and implement remedial actions• Continuously look for opportunities to improve service• develop and work with team to implement plan to re-organise and drive change (possibly across a customer account)• Ensure timely follow-up and resolution of compliance issues• Serve as Subject Matter Expert (SME)• Provide leadership and expertise in a specific CDM task or technology• Serve as customer site lead for one or more customers• Train and mentor junior DTL staff in DM expertise• may coordinate the work of more junior DTL staff• Independently maintain internal tracking databases and systems• Financial Management/Business Development Support:• Independently manage SOW/budget• Review financial reports on a monthly basis and participate in project reviews as requested• Identify out of scope tasks and track change orders to completion• Participate in pricing discussions across customer account• Serve as Project Manager for single service DM projects, including financial tracking, revenue recognition, and invoicing• Independently support RFP process (review RFP documents, pricing, attend bid defense)• Other:• Independently bring process improvements and solutions to the CDM team/CDM department• Lead a focus team or global or local best practice team• Communicate lessons learned and/or present in CDM workshop(s)• Manage the development and implementation of new technology or tool• Present at professional conferences and/or publish articles in professional journals• Provide review and expert opinion in developing, revising, and maintaining core operating procedures and work instructions• Perform other duties as directed by the functional manager Qualifications• Bachelor's Degree Health, clinical, biological or mathematical sciences, or related field Req• 5 years of direct Data Management experience with 3 or more years as a CDM project lead Pref• Previous experience and proven competence in managing delivery of multiple global trials through full DM life-cycle (i.e. large trials of at least 1000 patients). Demonstrated expert data management skills and advanced knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation, management of local laboratory data, and/or new technology). Previous experience and proven competence in handling complex customer negotiations and bid defense meetings independently. Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology. Knowledge of operating procedures and work instructions and the ability to apply them in practice. Knowledge of Good Clinical Practices and relevant regulatory guidelines. Excellent communication, interpersonal, customer service, and teamwork skills. Excellent organizational and problem-solving skills. Excellent project management skills. Ability to work independently. Comprehensive understanding of clinical drug development process. Ability to establish and maintain effective working relationships with coworkers, managers and customers. Previous experience and proven competence in managing delivery of multiple global trials through full DM life-cycle (i.e. large trials of at least 1000 patients). Demonstrated expert data management skills and advanced knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation, management of local laboratory data, and/or new technology). Previous experience and proven competence in handling complex customer negotiations and bid defense meetings independently. Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology. Knowledge of operating procedures and work instructions and the ability to apply them in practice. Knowledge of Good Clinical Practices and relevant regulatory guidelines. Excellent communication, interpersonal, customer service, and teamwork skills. Excellent organizational and problem-solving skills. Excellent project management skills. Ability to work independently. Comprehensive understanding of clinical drug development process. Ability to establish and maintain effective working relationships with coworkers, managers and customers. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewManage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team to provide high quality data management products that meet customer needs. Provide leadership to the team in the areas of project planning, execution, and close-out; Overview of financial management for data management activities; communications; and milestone deliverables. Perform role of Data Team Lead (DTL).  Essential Functions• Gather Study Set up requirements through discussion and communication with relevant stakeholders.• With Minimal guidance - support, overview of validation of new Device integrations.• Oversight & Perform regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor.• Ensure that all the deliverables are of expected quality standards and meet customer expectations.• With guidance, ensure service and quality meet agreed upon timelines and deliverables in contract/Scope of Work (SOW).• Support Training of New joiners.• Lead internal study meetings and internal/ sponsor audits and participate in Study Kick off meetings and other sponsor meetings.• Tracks and manages the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended as required.• With Guidance manage & oversight the implementation of new technology / database revisions.• Work closely with the programming team for process innovation and automation.• Be compliant to trainings and eSOP reading.• Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions.• Communication with Line Manager, and other team members across functions should be collaborative.• Perform other duties as directed by Line Manager. Qualifications• Bachelor's Degree In health, clinical, biological or mathematical sciences, or related field with proven experience in Data Management Req• 3 -4 years direct Data Management experience, including a minimum of 1 year as a CDM project lead. Pref• English Fluency Spoken and English Advanced• Advanced computer applications like Microsoft excel, word, Inbox etc Advanced• Should have Advanced understanding of Drug development lifecycle and Overall Clinical research process Advanced IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewProvide comprehensive data management expertise (defined as efficient and quality data management products) to Data Management (DM) team to meet sponsor and company needs. Perform Clinical Data Management and/or Coding activities, and may provide leadership either in the role of the Lead Coder or in a specific CDM task (e.g. Data Operations Coordinator (DOC) or lead a coding related task on a mega trial). Essential Functions• Serve independently as a Clinical Data Coder and/or Lead Coder or DOC for one or more protocols.• Manage delivery of coding activities and/or stand alone coding projects through full study life-cycle (with minimal guidance).• Validates/tests the coding application and programming of coding reports• may also test coding related datasets, coding related edits or any coding related programming activities.• Perform comprehensive data management and coding related tasks including, conducting data review and writing and resolving data clarifications.• Manage coding related project timelines with guidance from the DOC or Data Team Lead (DTL) or Manager.• Perform Serious Adverse Event (SAE) reconciliation activities.• May serve as a back-up for a Lead Coder, DOC or DTL.• Perform comprehensive quality control procedures, Assist in implementing new technology.• Independently bring coding and project related solutions to the DM team.• Handle audit requirements for respective studies including stand-alone coding projects as applicable.• Understand and comply with core operating procedures and work instructions.• Perform other duties as directed by the study team or Manager, or meet objectives as assigned• Develop and maintain good communication and working relationship with the team. Qualifications•  Pharmacy, dental, medical, nursing, life sciences or related field qualification or educational equivalent• 2 years of relevant experience or equivalent combination of education, training and experience.• Excellent knowledge of medical terminologies, pharmacology, anatomy and physiology.• In-depth knowledge of medical dictionaries used for coding (e.g., MedDRA, WHODD etc.).• Understanding of the Data Management process from study start-up through to database lock.• Ability to exercise excellent attention to detail and act independently with the initiative required to resolve problems.• Good understanding of database technologies related to data management and coding.• Knowledge of operating procedures and work instructions and the ability to apply them in practice.• Excellent written and oral communication skills in English language, organizational and leadership skills.• Ability to establish and maintain effective working relationships with co-workers, managers and clients.• LPN  - Licensed Practical Nurse - State Licensure   Req IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewManage single and multi-service projects, ensuring quality deliverables on time, within budget and to the customer’s satisfaction; Provide expert skills as part of a Clinical Data Management (CDM) team to provide quality data that meet customer needs; Provide leadership to the team in the area of coding, project planning and execution, financial management, communication and milestone tracking; Viewed as an expert in coding of clinical data; May perform the role of a Data Operations Coordinator (DOC), Data Team Lead (DTL), and a customer site lead or may be responsible for managing and delivering a program of studies for a customer. Essential Functions• Serve as an account lead, or internal or external point of contact on standalone coding studies or accounts• Manage the customer relationship for the project team including active participation in coding related customer negotiation on timeline, budgetary and other issues• Provide leadership and senior support to lead coders on one or more large global studies• Manage the relationship with a customer on a DM site level• Serve independently as a Lead Data Coder and/or Coding reviewer for one or more projects• May serve as a DOC or DTL for one or more projects• Perform comprehensive quality control procedures• Perform Serious Adverse Event (SAE) reconciliation activities• Collaborate with customers and develop solutions and action plans for issues, escalations and road blocks• Proactively identify, solve quality issues and deliver projects as per agreed timeline• Identify and provide due diligence for out of scope activity• Manage resource capacity for the project team• Mentor other team members in training and developing coding expertise• Independently bring project solutions to the Coding and CDM team• Identify and implement processes and quality improvement initiatives in the DM and coding function• Developing and implementing best practices in the team• Manage the development and implementation of new technologies• Demonstrate scientific and research temperament by presenting at, or participating in local and international forums• Responsible for identifying and implementing process improvements using established methods (principles of lean and six sigma) in collaboration with experts• Provide review and expert opinion in developing, revising, and maintaining standard core operating procedures and work instructions• Perform other duties as directed by the DOC, DTL or Manager, or meet objectives as assigned• Develop and maintain good communications and working relationships with the CDM team and client stakeholders Qualifications• High School Diploma or equivalent Pharmacy, dental, medical, nursing, life sciences or related field qualification or educational equivalent Pref• 7 years relevant experience in clinical trials within a similar function, including proven competence in managing the delivery of coding or/and other data management processes for multiple global projects, also including experience in handling complex customer negotiations and bid defense meeting. Pref• Excellent knowledge of Medical Dictionaries used for coding (e.g. MedDRA, WHODD, ICD9, etc.).• Excellent knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology required for many tasks.• Advanced knowledge of data management processes and systems and advanced ability to apply this knowledge in practice.• Excellent understanding of clinical drug development process (detail oriented).• Outstanding communication and organizational skills.• Proven leadership skills.• Good project management skills related to all phases of clinical studies.• Excellent knowledge of operating procedures and work instructions and the ability to apply them in practice.• Excellent English written and oral communication skills.• Ability to work on computer systems with ease and good working knowledge of computer programs.• Ability to exercise excellent attention to detail and act independently with the initiative required to resolve problems.• Ability to establish and maintain effective working relationships with co-workers and managers.• Comprehensive understanding of financial management concepts and able to interpret the financial information.• Able to present information effectively to individuals and groups.• Able to make independent decisions within scope of authority and considers the impact of decisions on other groups and people.• Able to motivate and lead teams to reach defined objectives.• Effective team management skills including conflict resolution, delegation, and change management.• Excellent interpersonal skills.• Able to establish trust and collaborative relationships with customers. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Essential Functions• Develops and delivers technology services through managed services project activities requiring general knowledge of IQVIA's products and technical expertise.• Responsible for identifying additional product/services opportunities for clients makes decisions within limited parameters under regular supervision.• Has broad understanding of quality standards and work requires minimal revision.• Assists in problem identification, system architecture definition, hardware/software specification and/or design, implementation, testing, client training and solution deployment.• Provides support on Service Requests using the incident management tool, CSM.• Coordinates the routing and handling of Requests For Change to the next level of support under regular supervision.• Escalates issues relating to product support or product operations to the next level of support.• Project management activities include interaction with company and client managers and cost/schedule monitoring. Qualifications• Bachelor's Degree Computer Science, a related field, or equivalent experience Req IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Essential Functions• Develops and delivers technology services through managed services project activities requiring general knowledge of IQVIA's products and technical expertise.• Responsible for identifying additional product/services opportunities for clients makes decisions within limited parameters under regular supervision.• Has broad understanding of quality standards and work requires minimal revision.• Assists in problem identification, system architecture definition, hardware/software specification and/or design, implementation, testing, client training and solution deployment.• Provides support on Service Requests using the incident management tool, CSM.• Coordinates the routing and handling of Requests For Change to the next level of support under regular supervision.• Escalates issues relating to product support or product operations to the next level of support.• Project management activities include interaction with company and client managers and cost/schedule monitoring. Qualifications• Bachelor's Degree Computer Science, a related field, or equivalent experience Req IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewPerforms advanced development, support and implementation of complex software systems using specialized domain knowledge and highly-developed business expertise.Evaluates business and software industry trends and suggests improvements to processes, products and services. Essential Functions• Performs advanced development, support and implementation of complex software systems using specialized domain knowledge and highly-developed business expertise.• Works at all layers of the application stack including front-end user interface and backend development.• Leads large and/or multiple teams within job function for projects or programs with high complexity and visibility.• Evaluates business and software industry trends and suggests improvements to processes, products and services.• Focuses on software quality standards for all aspects of work and sets standards for others.• Establishes advanced software test standards and methods and conducts complex software tests. Qualifications• Bachelor's Degree Computer Science, a related field, or equivalent experience Req• Eight (8) years of systems analysis and software development experience Req• IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

About IQVIA Digital IQVIA Digital is transforming healthcare marketing through data-driven, privacy-first, omnichannel engagement solutions. Powered by IQVIA’s industry-leading data, identity, and measurement capabilities, Media OS serves as the intelligent operating system enabling healthcare marketers to plan, activate, measure, and optimize campaigns within a unified platform. We are seeking a visionary and execution-oriented Senior Director, Product – Media OS to lead the next evolution of our flagship platform and drive innovation at the intersection of healthcare, data, and advertising technology. Position Overview The Senior Director, Product – Media OS will own the vision, strategy, roadmap, and market success of IQVIA Digital’s flagship healthcare marketing platform. This leader will drive the transformation of Media OS from a unified omnichannel marketing platform into an intelligent, AI-powered audience and activation ecosystem that enables healthcare organizations to deliver highly personalized, privacy-compliant marketing experiences at scale. The ideal candidate brings deep expertise in AdTech, martech, digital platforms, data-driven SaaS products, and omnichannel marketing ecosystems, combined with a proven ability to lead cross-functional teams and deliver measurable business impact. Key Responsibilities Product Vision & Strategy Define and lead the long-term product vision for Media OS, aligning with IQVIA Digital’s mission to deliver personalized, data-driven healthcare marketing solutions.Drive the evolution of Media OS into an intelligent, AI-powered audience and activation platform.Develop product positioning that differentiates Media OS through identity, data intelligence, and omnichannel orchestration.Establish strategic priorities and investment plans that support growth, innovation, and market leadership.Product Roadmap & Innovation Own and execute the end-to-end product roadmap across: Campaign planning and forecasting capabilities, including AI-driven recommendations.Audience development, segmentation, direct-to-consumer workflows, and federated audience models.Identity and data infrastructure, including expansion of identity graph capabilities and enterprise-wide data accessibility.Activation solutions, progressing from multi-DSP orchestration to AI-powered optimization and decisioning.Lead innovation initiatives focused on: AI-driven campaign optimization and automated decisioning.Closed-loop marketing and performance intelligence.Real-time analytics and adaptive campaign management.Seamless user experiences across planning, activation, measurement, and optimization workflows.Platform & Ecosystem Leadership Lead the development of Media OS as an open, multi-platform ecosystem supporting diverse activation partners and media channels.Drive integrations and strategic partnerships across programmatic, social, connected TV (CTV), email, and endemic media environments.Ensure platform scalability, reliability, and flexibility to support enterprise-level healthcare marketing campaigns.Anticipate market trends and evolving customer needs to maintain competitive advantage.Commercial Strategy & Growth Partner closely with Sales, Marketing, and Client Success teams to: Refine product packaging, pricing, and go-to-market strategies.Accelerate platform adoption among agencies and pharmaceutical clients.Develop platform-led growth initiatives that drive revenue expansion.Support integrated campaign solutions and new market opportunities.Champion customer success by: Delivering measurable improvements in reach, engagement, efficiency, and campaign performance.Demonstrating the value of consolidated workflows and reduced operational complexity.Ensuring strong customer adoption and retention outcomes.Cross-Functional Leadership Lead and mentor high-performing product teams across audience, identity, activation, workflow, and measurement domains.Collaborate with Engineering, Data Science, Design, Sales, Marketing, Operations, and Client Success teams to execute strategic initiatives.Foster a culture of innovation, accountability, and customer-centric product development.Align organizational stakeholders around product priorities, investments, and business objectives.Thought Leadership & Industry Influence Represent IQVIA Digital as a recognized industry leader in healthcare marketing innovation.Advocate for data-driven personalization, identity-based marketing, and AI-powered advertising technologies.Share insights through industry events, client engagements, conferences, and executive forums.Help shape the future of privacy-first, healthcare-focused marketing platforms.Required Qualifications 12+ years of product management and product leadership experience in:Advertising technology (AdTech)Marketing technology (MarTech)Digital platformsData-driven SaaS environmentsProven success building and scaling enterprise platforms supporting planning, activation, and measurement workflows.Deep expertise in:Programmatic advertising ecosystems and DSPsIdentity resolution and identity graph technologiesData platforms and audience modelingOmnichannel marketing strategiesDemonstrated ability to:Lead large-scale cross-functional organizationsTranslate strategic vision into measurable business outcomesInfluence senior executives and key stakeholdersOperate effectively in complex, regulated industriesPreferred Qualifications Advanced degree (MBA or related graduate degree).Experience in healthcare, life sciences, pharmaceutical, or highly regulated industries.Familiarity with AI/ML-based optimization, prediction, and recommendation systems.Experience building open-platform ecosystems and partner integration strategies.Knowledge of privacy regulations and healthcare marketing compliance requirements.What Success Looks Like In this role, you will: Establish Media OS as a market-leading operating system for healthcare marketing.Deliver seamless orchestration across channels, partners, and activation platforms.Accelerate adoption among agency partners and direct pharmaceutical customers.Drive meaningful growth in platform usage, revenue, and customer satisfaction.Differentiate IQVIA Digital through industry-leading data, identity, and performance capabilities.Enable AI-powered optimization that delivers measurable improvements in campaign effectiveness and efficiency.Why Join IQVIA Digital? At IQVIA Digital, you'll have the opportunity to help define the future of healthcare marketing. This is a rare opportunity to lead a category-defining platform at the intersection of healthcare, data, identity, and advertising technology. You will play a pivotal role in transforming Media OS into an intelligent, adaptive, and AI-powered marketing ecosystem that creates measurable value for healthcare organizations and patients alike. Join us in building the next generation of privacy-first, data-driven healthcare marketing solutions. This is a remote / WFH position open to applicants within the United States. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $140,100.00 - $390,400.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Manager, Database Management Systems Job SummarySeeking an experienced clinical data professional to lead database management and clinical data standards activities supporting global clinical trials. This role will serve as a subject matter expert in clinical data standards, Medidata Rave global library development, and SAS programming, partnering with cross-functional teams to ensure high-quality, standardized clinical data collection and reporting. Key Responsibilities Lead development and maintenance of global clinical data standards, including CDISC-compliant operational data mappings and SDTM standards.Build and maintain Medidata Rave global library objects, including eCRFs, edit checks, and CRF Completion Guidelines.Develop SAS programs for edit checks, data imports, listings, custom reports, and clinical data validation.Create and manage clinical datasets from raw data using Base SAS, Advanced SAS, Macros, PROC SQL, and SAS ODS.Support CRF design, annotated CRFs, data mapping specifications, and define.xml requirements.Collaborate with Clinical Data Management, Clinical Operations, EDC Programming, vendors, and CRO partners to ensure consistent standards implementation.Drive process improvements, support governance committees, and provide mentorship to junior team members.Ensure compliance with CDISC standards, GCP, ICH guidelines, and regulatory requirements.Required QualificationsStrong clinical domain knowledge with a solid understanding of clinical trial phases.Prior work experience must be within the clinical research, pharmaceutical, biotechnology, healthcare, or CRO industry.Hands-on experience programming Edit Check Listings using SAS.Experience with Data Import Programming using SAS.Experience utilizing SAS Output Delivery System (ODS) to generate reports in RTF, PDF, and HTML formats.Experience reading raw data files, creating data structures, handling missing values, troubleshooting programming errors, and managing clinical data.Experience appending and concatenating SAS datasets.Proficiency developing reports using PROC PRINT, PROC FREQ, PROC MEANS, PROC TRANSPOSE, and PROC SQL.Strong programming experience with SAS Macros and SQL.Experience creating SAS datasets from raw clinical data, including status and efficacy datasets.Ability to develop project-specific macros and formats, load client data from external platforms, and prepare datasets for client delivery.Experience creating clinical listings and custom reports based on business requirements.Knowledge of Vendor Import Programming.Strong technical expertise in Base SAS, Advanced SAS, SAS Macros, SAS SQL, and SAS Grid.Ability to develop code using Base SAS programs, SAS procedures, and standardized macros.Excellent written and verbal communication skills.Preferred Qualifications Experience with CDASH and ADaM standards.Extensive Medidata Rave global library development experience.Knowledge of MedDRA, WHODrug, annotated CRFs, and data mapping specifications.Experience with Veeva, Medrio, Oracle Clinical, TrialGrid, or similar EDC systems.Demonstrated ability to lead cross-functional initiatives in a global clinical development environment.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $84,600.00 - $211,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job Level: Senior Director, Drug Development Location: Home-based in Europe Job Overview: Manages a department or small unit.; Provide leadership and advice on the development of optimum strategies for drug development, product lifecycle management and portfolio management to meet pharmaceutical and biotechnology customer goals (such as strategic leadership of clinical development plans, go/no go decisions, in-licensing, out-licensing, accelerated time to market, etc).; Provide medical, clinical, scientific, regulatory, and product development leadership and consultancy expertise to support strategic business activities and investment opportunities.; Participate in all aspects of Strategic Drug Development and lead the implementation of mission, goals and objectives, development of policies, procedures and standards for the department. ; Provide thought leadership in pharmaceutical product development by preparing publications, white papers, and blogs in areas of expertise and by participating in scientific conferences and webinars, as appropriate. Essential Functions: Evaluate and develop product development strategies for pharmaceutical products (drugs, biologics, advanced therapies) focusing on clinical-commercial convergence that encompasses all phases of development from discovery to market, including preclinical strategy, clinical strategy, regulatory strategy, and commercial strategy. Support engagements with regulatory authorities (e.g., FDA, EMA) on behalf of customers, across the lifecycle of drug development from pre-clinical to licensing, including contribution to briefing documents and other meeting materials, and attendance and contribution to meetings and other interactions. Lead assessments of risk and probability of regulatory success and development of mitigations for candidate pharmaceutical products, including providing regulatory contributions to indication prioritization exercises, development strategy evaluations and gap analyses, due diligence, and similar activities. Support the innovative development of compounds to maximize technical, regulatory, and commercial success, including contribution to the development of Target Product Profiles (TPPs), Clinical Development Plans (CDPs), clinical study designs, synopses, and protocols, as appropriate. Strategic leadership of the development of regulatory submissions, including INDs, marketing/licensing authorizations (NDA/BLA/MAAs), special designations (orphan drugs, pediatrics plans, “fast-track”, “break-through” etc.…). Ensure high-quality, well-reasoned, objective deliverables (using data-driven design, where available and appropriate) that meet the highest standards of medical, ethical and scientific integrity and conduct. Assume the role of customer senior management as requested, including membership of virtual cross functional drug development teams. Provide drug development expertise to support strategic business activities and investment opportunities. Assist in the development of programs to maximize the organization’s growth and profitability. Ensure Customer Satisfaction by working closely with Senior Management, CRO Operations, Therapeutic Units, and other Operations Heads to ensure optimum strategic consultancy to customers. Serve as a key resource and participate in strategic business development activities including presentations to prospective clients, professional meetings or other business development activities for IQVIA Strategic Drug Development. Provide internal and external therapeutic and pharmaceutical development-related educational services in support of all branches of IQVIA business. Attend key scientific meetings/conferences and keep abreast of relevant scientific publications to maintain awareness of current scientific developments and progress in drug development methodology As appropriate, represent IQVIA or the partner in such meetings. Develop and maintain ongoing relationships with pharmaceutical and biotechnology companies, key opinion leaders identify new business opportunities. Compliance with all business office requirements for tracking time and effort. Qualifications: Masters degree or higher or the equivalent combination of education, training and experience. Typically requires 15-20+ years relevant clinical research experience with multi-regional and global focus including significant experience in senior strategic role. Requires broad management and leadership knowledge to lead multiple job areas, the ability to influence others to accept practices and approaches. Expertise in Excel and PowerPoint. Strong strategic thinking, analytical and communication skills and ability to thrive in a culture of achievement. Client-focused and consultative approach for project management - not just an order taker but is able to suggest alternate approaches and provide strategic insights that meet client needs. Demonstrates a strong command of a variety of analytical and market research techniques. Sought out by clients (internal and external) as an analytical expert and, more importantly, as a strategic advisor. Grasps key issues quickly, understands the "big picture", and links market research insights to larger business issues relevant to client needs. Demonstrates excellent written and verbal communication skills and is effective in a variety of presentation settings. Has a strong commitment to quality. Has a proven track record of meeting or exceeding goals. Has broad management knowledge to lead teams and leadership knowledge to lead multiple job areas. Has ability to influence others to accept practices and approaches. #LI-Remote#LI-HARJINDERBHUMVRA IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The Senior Manager, Biosamples Operations Lead will own end-to-end biosample operations across assigned studies/programs - from operational feasibility, vendor selection, and execution of biosample operations activities through analysis and data delivery. As the primary point of contact for the Study Team on all biosample operations activities, including biomarker and bioanalytical operational activities, you will ensure every biosample is collected, processed, and delivered to the highest quality and regulatory standard, while keeping a sharp focus on patient burden and operational efficiency. Main Responsibilities• Provides strategic and expert input for the operational feasibility, implementation and execution of the biosample operations activities in assigned clinical studies/programs.• Manages biosample management activities in clinical studies with low to moderatecomplexity, risk, impact and reach.• Accountable for planning, implementation and execution of biosample operations activities, ensuring proactive risks and issues management and alignment with overall clinical study timelines• Owns biosample operations plan and is responsible for its maintenance and adjustments during clinical study conduct.• Leads cross-functional biosample operations team and manage team meetings to review status of biosample operations activities, discuss risks/issues and agree on appropriate mitigation.• Acts as the single point of contact (POC) in Study Team on biosample operations related aspects (including biomarker and bioanalytical activities). Ensures timely status updates and escalation of risks/issues to the clinical Study Team.• Contributes to central lab or assay lab vendor selection and qualification.• Oversees Central lab set-up, kit management, and ongoing study level vendor performance.• Manages CRO and central lab interfaces to ensure cross-functional alignment on deliverables.• Maintains a patient focus approach while delivering the complex requirements of a clinical study, balancing patient burden, sampling requirements, the complexity of collection and the cost implications.• Responsible for overseeing the biosample lifecycle and compliance to ensure that the biosamples are collected, processed, analysed and stored with the highest degree of quality and according to applicable regulations.• Reviews and provides input to protocols, ICFs, lab manuals, and regulatory submissions.• Leads budget planning & forecasting for biosample activities of assigned studies.• Ensures all activities comply with ICH-GCP, GCLP, biobanking policies, and applicable ethical standards.• Leads audit and inspection readiness; act as interviewee and prepare regulatory responses.• Impacts the successful delivery of a program/study and ensure optimized execution of the biosample/biomarker operations strategy on time, within budget and required quality.• Leverages strategic operational knowledge and serves as subject matter expert for current biosample management processes and regulations.  Required Skills and Education• Minimum Bachelor’s degree in Biology, Pharmaceuticals, or Life Sciences or related field. • At least 6+ years of experience in Clinical Operations with a focus on Biosamples management activities in a CRO or pharma setting.• Proven track record in central lab oversight, vendor management, and Phase I–III biosample logistics. • Experience in CDx development and/or Bioanalytical requirements, would be advantageous.• Broad experience across multiple therapeutic areas, trial phases and biosample lifecycle management.• Comprehensive and working knowledge of GCP, GCLP guidelines and other relevant regulations and requirements for the collection, analysis and storage of clinical biosamples.• Very good knowledge of biosample management related systems and technologies (LIMS, BRICK, CTMS, etc)• Demonstrated experience in effectively collaborating with other functions in a complex matrix organization. • Very good command in English language. Please note this role is not eligible for the UK visa sponsorship. Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewActs as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs Senior Review of straightforward medical writing deliverables. Negotiates timelines and discusses/resolves customer comments.Provides written and verbal feedback to junior staff, and to customers when appropriate. Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or technical writing. Essential Functions Take a leading role in preparing assigned documents, including, but not limited to, confirming the scope of the task, confirming templates and specifications, negotiating and adhering to timelines, organizing document reviews, communicating directly with the customer. Plan and organize workload for assigned projects and tasks: identify project needs, track timelines and implement customer requests. Lead meetings on more challenging topics independently. May present on standard Medical Writing processes at full-service bid defense meetings. Assist in the training and development of junior staff, either formally as an assigned mentor or ad hoc for local colleagues or others. May develop and deliver training to the global team on a topic he/she has specific expertise in. May input into and deliver presentations on Medical Writing to other IQVIA groups. May act as Project Manager for a more complex but single Medical Writing project which includes Project Finance/Invoicing responsibilities. Complete project finance activities, including monitoring and forecasting budgeted hours. Propose, review and approve budgets and costings for routine projects, including estimation of hours needed for Medical Writing tasks. May take on a small customer lead role or assist an established partnership lead in their role. May represent region or site on a Medical Writing initiative or cross-functional initiative. Facilitates and brainstorms the identification of new ideas. May represent Medical Writing at a general capabilities audit. Qualifications Bachelor's Degree Bachelor's Degree in life sciences related discipline or related field Master's Degree Master's Degree in life sciences related discipline or related field  Ph.D. Ph.D. in life sciences related discipline or related field Typically requires at least 3 years of highly relevant experience and related competency levels. In-depth knowledge of the structural and content requirements of clinical study reports, protocols, and similar documents and ability to identify deficiencies, errors, and inconsistencies in a protocol or report. Good understanding of common statistical methods used in clinical trials and/or interpretation of their results. Ability to effectively review a statistical analysis plan and to identify deficiencies, errors, and inconsistencies in statistical output Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner. Significant experience as a lead writer in preparing CSRs and protocols, with consistently positive feedback from customers and colleagues. In depth knowledge of drug development, medical writing, and associated regulations. Good understanding of statistical principles and of medical terminology across a range of therapeutic areas. Excellent written and oral communication skills including grammatical/technical writing skills. Excellent attention to detail and accuracy. Confident and effective communication and negotiation skills with customers and project managers. Able to deliver difficult messages in constructive manner. Demonstrates initiative and sound judgement when faced with less familiar project/document situations or challenges. Demonstrated abilities in collaboration with others and independent thought. Demonstrates confidence and maturity in most routine medical writing situations. Demonstrates good judgement in requesting input from senior staff. Ability to establish and maintain effective working relationships with coworkers, managers and customers. Ability to effectively manage multiple tasks and projects. Ability to proactively evaluate risks and potential issues and seek solutions and discuss appropriately with colleagues and customers. Must be computer literate. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Voor een opportuniteit bij één van onze klanten zoekt IQVIA een farmaceutisch afgevaardigde. Je komt terecht bij een jong en dynamisch bedrijf met een uitstekende reputatie en een sterke groei. De organisatie is marktleider binnen haar domein en staat bekend om haar familiale en warme bedrijfscultuur, met weinig verloop en collega’s die al jarenlang met engagement meebouwen aan het succes. Wat houdt de job in? Bezoeken van zelfstandige apotheken en apotheekgroeperingen binnen jouw regioPromoten en positioneren van een sterk portfolio binnen de oftalmologie (o.a. oogdruppels, droge ogen en artificiële tranen), met focus op OTC‑productenOpbouwen en onderhouden van duurzame relaties met apothekers en hun teamsNauw samenwerken binnen een stabiel en ervaren teamActief meedenken over groeikansen en het vergroten van het marktpotentieelRealiseren van gemiddeld 6 kwalitatieve bezoeken per dagWat breng jij mee? Je bent matuur, verantwoordelijk en werkt zelfstandigJe wil echt mee het verschil makenJe bent proactief, ondernemend en neemt graag initiatiefJe hebt een commerciële mentaliteit en denkt graag strategisch meeJe communiceert vlot in NederlandsJe spreekt vloeiend EngelsWat hebben we jou te bieden? Een competitief salaris, afgestemd op jouw ervaringEen aantrekkelijk pakket aan extralegale voordelen, inclusief bedrijfswagen met laadkaart, groeps‑ en hospitalisatieverzekering, …Een uitdagende functie met veel autonomie binnen een groeiende en stabiele omgevingGrondige begeleiding en opleiding, zodat je sterk van start kan gaan en je verder kan ontwikkelenKlaar om impact te maken? Solliciteer nu!  #LI-MB1 #LI-CES IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.