IQVIA

Location: Singapore, Shanghai, Hong Kong, Tokyo, Sydney Function: Advisory Services, Global Data, Technology, and Advisory Services (DTAS) About the Role We are seeking inspirational leaders to shape and elevate our Global enterprise Data, Technology, and Advisory Services presence across the United States, Japan, and Asia/Pacific. In an increasingly complex market, our HQ, regional HQ, and enterprise clients face deep challenges. Cluster Leads will serve as trusted partners to these clients, developing deep understanding of their challenges and consistently earning IQVIA the opportunity to support them. Globally, IQVIA’s clients face daunting challenges: declining R&D productivity, relentless cost pressure, and deteriorating operating economics. Clients urgently need to evolve their models to achieve greater agility, speed, and commercial precision. By combining its unique proprietary data assets, its deep expertise in data architecture and analytics, and its global advisory services, IQVIA has a unique opportunity to be a partner of choice to clients as they navigate this transformation. Earning this opportunity requires strong front-line leaders with a proven ability to build intimacy and trust with senior decision-makers. As the Cluster Lead for JAPAC, you will serve as the senior client-facing DTAS leader for your region, shaping commercial strategy, driving growth, and ensuring exceptional delivery across a cross-functional team. You will act as a trusted advisor to senior stakeholders, deepen client intimacy, and champion integrated solutions across a range of asset and above-asset priorities. You will bring a partner-level presence, demonstrating the strategic influence, commercial acumen, and people leadership central to the success of professional service firms. What You’ll Do: Be the senior face of DTAS for your Cluster, trusted by SVP‑level and other senior stakeholders as a strategic advisor, sounding board, and thought‑partnerSet and own the Technology and Advisory Services growth agenda for your cluster — defining key client priorities, shaping large‑scale opportunities, and driving year‑over‑year expansion and customer satisfactionModel deep client intimacy and exemplify best‑in‑class client leadership, operating close to your customers, regularly present onsite, and deeply embedded in their strategic prioritiesFacilitate cross‑functional collaboration to leverage expertise within Advisory Services (brand strategy, portfolio strategy, value & access, digital health) and the broader DTAS portfolio (data strategy, architecture, outsourcing, technology) — fostering a culture of excellence, collaboration, and innovation.Ensure high-impact delivery, ensuring work is insight‑rich, strategic, rigorous, and reflective of the high expectations of our customers; further, you will work with your peers across DTAS to ensure a consistent and high standard of deliverable quality and customer experienceCultivate and nurture top talent, coaching and elevating emerging leaders, providing crisp direction, and creating an environment where teams thrive and grow.Inform and deepen IQVIA’s Thought Leadership and insight, collaborating with IQVIA’s Thought Leadership organization and front-line practitioners to shape, refine, and communicate strategic insights about critical issues facing our clientsInfluence across the enterprise, collaborating closely with other DTAS leaders, GADs, Client Partners, and senior executives to lead and shape client engagement on priority topics and accelerate impactOwn your business, delivering on customer revenue and margin targetsWhat You Bring Experience operating at Senior Principal or Partner level in a top-tier consulting environment or comparable internal strategy/advisory leadership.Broad capabilities and experience across key client priorities, including technology, transformation, commercial strategy, and health care.A track record of owning and growing major client relationships, with deep comfort engaging senior decision-makers.Strong commercial acumen: opportunity shaping, complex pursuit leadership, customer value articulation, senior stakeholder orchestration.A leadership style that inspires confidence, unlocks team performance, and elevates the bar for consulting excellence.Ability to lead, inspire, and develop multi-disciplinary teams in a dynamic, evolving environment.Passion for client engagement and a pronounced ability to operate with high presence on client site, building trust through proximity, responsiveness, and insight.Deep intellectual curiosity and learning agility: a pronounced ability to learn and digest new content and to apply it to customer challenges and prioritiesExceptional communication, storytelling, and influence skills — able to simplify, inspire, and drive alignment across diverse groups.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.

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 88.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für ein spannendes Projekt im Bereich Immunologie/Impfstoffe suchen wir Pharmaberater (m/w/d) zum nächstmöglichen Zeitpunkt Ihr Gebiet: Bautzen, Görlitz, Hoyerswerda, Weißwasser, Zittau, Löbau, Rothenburg   Das sind Deine Aufgaben: Durch die intensive Betreuung ausgewählter Ärzte förderst Du die Verordnung Deiner Präparate und trägst so maßgeblich zum Unternehmenserfolg bei. Du setzt als Experte auf der Basis Deines Fachwissens Beratungsstrategien erfolgreich um und überzeugst so Deine Ansprechpartner. Du findest mit Deinen Gesprächspartnern innovative Therapiekonzepte in anspruchsvollen Indikationen. (optional: zum Wohle des Patienten/für den Patienten/und trägst somit zur Gesundheit und dem Patientenwohl bei) Du führst regionale und zentrale Fortbildungsveranstaltungen in enger Abstimmung mit dem Regionalleiter und Deinem regionalen Team durch. Das bringst Du mit: Du hast bereits Erfahrung als Pharmaberater, Pharmareferent oder Klinikreferent in verschiedenen Indikationen gesammelt. Du verfügst über eine Naturwissenschaftliche Ausbildung (idealerweise Hochschulabschluss) oder Ausbildung zum Geprüften Pharmareferent (m/w/d) gemäß §75 AMG Als durchsetzungsstarke Persönlichkeit und erfahrener Netzwerker verstehst Du es, dich und Deine Ansprechpartner zu begeistern. Du möchtest etwas bewegen – für Dein Präparat, für dich selbst und vor allem für betroffene Patienten. Ausgeprägte kommunikative Fähigkeiten sowie die Bereitschaft, eigenverantwortlich und ergebnisorientiert zu arbeiten. Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] #LI-CES #LI-DNP #LI-SS2 #Pharmaberater #Biologie #Chemie #Pharmareferent #BTA #CTA #PTA #Oecotrophologie #Pharmazie #Pharma-Außendienst 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 OverviewDirect and manage project(s) and/or multi-project programs ensuring the quality of deliverables are on time and within budget.  Ensure that all project work is completed in accordance with SOPs, policies and practices. Essential Functions• Manage the scope of work, objectives, timelines, quality of deliverables, and all other project management activities for the project(s) and/or multi-project program(s).• Serve as primary project contact with internal and external customers to ensure appropriate communication channels are maintained and reporting schedules adhered to.• Develop project plans for all phases of the project and associated deliverables.• Review project budget and scope of work, including management of project budget(s) to meet financial and company goals proactively ensure adherence to change control processes.• Supervise maintenance of project management information and data tracking systems.• May direct project activities for team members regarding their project-oriented tasks to ensure that project milestones are met.• Evaluate impact of risks, develop and implement quality and risk management plans for minimizing impact on project objectives and deliverables.• Continually review and ensure adequate internal and external resources are available to meet project deliverables and milestones.• Develop and implement continuous improvement processes for assigned projects.• Participate in RFP development and sales/proposal presentations; provides input on scope and budget development.• Provide technical expertise and project management experience to Project Manager(s) and training efforts.• Serve as a project management liaison with other groups within IQVIA. Qualifications • Bachelor's Degree minimum• 7+ years experience in Clinical Trial Operations including at least 3 years in a role of primary responsibility for clinical trial execution and management• Deep U.S. institutional engagement experienceProven ability to build and sustain relationships with operational leaders and high-performing investigators and within key academic centers, community sites, with a track record of translating those relationships into strong enrollment outcomes. • Strategic partnership with Medical Science Liaisons Experience working closely with MSLs to engage investigators, inform site selection, and strengthen overall site strategy. Candidates should be able to articulate how Clinical and Medical Affairs collaboration has enhanced site performance and enrollment and the distinct remits of each role. • Strength in site strategy and feasibilityAbility to proactively identify and prioritize the right sites using data, institutional knowledge, and field insights (including MSL input), and to continuously optimize the site mix based on performance. • Ownership of U.S. enrollment performanceDemonstrated success driving enrollment through thoughtful site engagement, patient access strategies, and targeted institutional partnerships, including attention to diverse patient populations. Operates at a portfolio and strategy level, not task execution • Country-level strategic thinking within global trialsExperience translating global study strategies into effective U.S. execution, while serving as the voice of U.S. sites and investigators to global teams. 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 $82,600.00 - $229,900.00. 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.

The Data Security Architect role presents a foundational opportunity to establish and lead IQVIA’s Data Security Architecture practice. As a data-driven global life sciences company, IQVIA manages one of the world’s most complex and sensitive healthcare data estates — spanning clinical research, real-world evidence, commercial analytics, and patient-level health information across dozens of markets worldwide. IQVIA’s data environment reflects the scale and complexity of a global enterprise with a significant M&A history: a hybrid estate encompassing on-premises data centers, multi-cloud infrastructure, modern analytical platforms, and a broad portfolio of operational and data movement technologies. Sensitive data — including PHI, PII, pharmaceutical client intellectual property, and clinical trial data — is distributed across this estate and must be protected consistently, at scale, and in alignment with a growing set of global regulatory requirements. The Data Security Architect will define how IQVIA discovers, classifies, governs, and protects its data assets across the enterprise — building the architecture, standards, and program foundations that underpin regulatory compliance, vendor governance, and AI security as IQVIA advances its data platform strategy. This role sits within the global Information Security organization and operates in close partnership with the Data Office, Cloud Security, Application Security, IAM, Legal, Privacy, and Compliance. It carries direct engagement with senior data platform and business stakeholders across IQVIA’s global business units. Principal Responsibilities Define and own IQVIA’s Data Security Architecture strategy, establishing a formal program from the ground up that is aligned to IQVIA’s hybrid, multi-cloud, and post-M&A data environment and the Data Office’s strategic platform direction.Lead the evaluation, selection, and implementation of a Data Security Posture Management (DSPM) platform, encompassing sensitive data discovery, classification, exposure analysis, access risk assessment, and continuous posture monitoring across on-premises and cloud-hosted data environments.Develop and maintain a comprehensive data security architecture covering data classification frameworks, data access governance, encryption standards, tokenization, masking, and data loss prevention controls across structured and unstructured data at scale.Partner closely with the Data Office to align data security architecture with enterprise data governance and platform strategy, ensuring security controls are embedded in data lifecycle management across analytical, operational, and AI workloads.Define security architecture standards and guardrails for IQVIA’s strategic data platforms, including cloud-native analytical environments (Snowflake, Databricks), data movement and transformation tooling, and operational database platforms, ensuring consistent security posture across a diverse and evolving estate.Provide data security architecture input and oversight for platform migrations, legacy system decommissions, and M&A integration programs — assessing inherited data estates for sensitive data exposure, access control gaps, and regulatory risk, and defining remediation roadmaps aligned to integration timelines.Define IQVIA’s data security approach for AI and LLM-integrated platforms, establishing policy and technical controls governing the safe use of AI capabilities embedded in or connected to data platforms, including controls around data inputs, model outputs, and prevention of regulated data exposure in AI workflows.Architect data security controls for advanced analytics and AI/ML pipelines, including protection of training datasets, model pipeline integrity, RAG data source governance, and controls preventing unauthorized use of sensitive data in AI-connected systems.Develop and govern IQVIA’s enterprise data classification taxonomy and policy framework, working with Legal, Privacy, Compliance, and business data owners to define classification tiers, handling requirements, and technical enforcement mechanisms across business units and regions.Establish data access governance principles across IQVIA’s data platforms, including least-privilege access models, periodic entitlement reviews, and integration with IAM and PAM controls at the data tier.Define encryption and key management architecture for data at rest and in transit across on-premises databases, cloud storage, data warehouses, and analytical environments, with particular attention to PHI and cross-border data transfer requirements.Provide security architecture input to data platform vendor evaluations and contract negotiations, ensuring security requirements, data-use restrictions, telemetry controls, and audit rights are appropriately represented.Support regulatory compliance requirements across GDPR, HIPAA, CCPA, GxP, and applicable regional data protection regimes, translating regulatory obligations into architectural controls and providing assurance evidence for audits and assessments.Define metrics, KPIs, and reporting frameworks for data security posture, providing actionable visibility to CISO leadership and Data Office stakeholders on data risk, program coverage, and maturity progression.Required Experience and Qualifications 6–10 years of progressive experience in Information Security, Data Security, Security Architecture, or related technical roles, with demonstrated ownership of data-centric security programs or initiatives.Deep knowledge of data security architecture principles, including data classification, access governance, encryption, tokenization, masking, and data loss prevention across hybrid environments spanning on-premises data centers and multi-cloud platforms.Hands-on experience with enterprise-scale cloud data platforms (such as Snowflake, Databricks, or equivalent), with the ability to design and assess security controls including governance, access policy, and data sharing frameworks.Experience with cloud environments (Microsoft Azure and/or Amazon AWS), including securing data services across IaaS, PaaS, and cloud-native analytical platforms.Experience evaluating or deploying DSPM, data governance, or data classification platforms such as Varonis, Securiti, Cyera, Microsoft Purview, BigID, or equivalent.Working knowledge of IAM and access governance principles as applied to data platforms, including RBAC, ABAC, and entitlement management across analytical and operational environments.Experience conducting security architecture reviews in complex, heterogeneous data environments, including post-M&A assessments, legacy platform migrations, or on-premises data center programs.Strong understanding of regulatory frameworks governing sensitive data, including HIPAA/HITECH, GDPR, CCPA, and GxP, with the ability to translate regulatory requirements into architectural controls across a diverse platform estate.Foundational to intermediate knowledge of AI and ML security considerations, including LLM application risks, model pipeline security, and the data protection implications of AI features embedded in or connected to enterprise data platforms.Demonstrated ability to operate at the intersection of security and data platform teams, communicating architecture decisions to data engineers, platform architects, business data owners, and senior stakeholders.Experience within regulated industries — life sciences, healthcare, or financial services — with direct exposure to clinical, patient-level, or pharmaceutical data security requirements is preferred.Bachelor’s degree in Computer Science, Information Security, Data Management, or equivalent practical experience is preferred.Relevant certifications such as CISSP, CISM, CDPSE, CCSP, AWS/Azure Security Specialty, or CIPP/E are preferred but not mandatory.Working knowledge of data governance and security frameworks such as NIST Privacy Framework, DAMA-DMBOK, ISO 27001, or similar is an advantage.Strong written and verbal communication skills, including experience producing architecture documentation, security standards, and executive-level reporting for senior leadership and governance forums.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 $112,200.00 - $312,700.00. 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.

We are seeking Project Management Analyst to join IQVIA Laboratories at Columbia, MD.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary:Support the planning, coordination, and delivery of non-complex projects by helping maintain scope, schedules, and success metrics. Contribute to project execution by monitoring risks, supporting stakeholder communication, and helping drive project outcomes aligned with operational and compliance standards. What You'll Be Doing:Assist in maintaining and validating project scope, plans, and schedulesSupport monitoring of project risks and communicate updates to relevant stakeholdersHelp manage project delivery processes, scope, and costs for non-complex projects under supervisionExecute project communication plans and help maintain stakeholder relationshipsSupport organizational change efforts by identifying project impacts and building awarenessEvaluate project results against defined success metrics and recommend process improvementsContribute to team reporting and guidance metrics to support project visibility and performance What We Are Looking For:Bachelor's Degree in Computer Science, or equivalent experience requiredEighteen (18) months of experience in a systems development environment requiredExperience supporting project scope, planning, and schedule validationUnderstanding of project delivery processes, cost tracking, and risk monitoringOther Equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Good technical and commercial awarenessGood communication skillsAbility to build stakeholder relationships and support cross-functional collaborationAbility to assess project outcomes and identify opportunities to improve productivity and end results What We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.To learn more about our benefits, visit https://jobs.iqvia.com/benefits.If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!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 $49,800.00 - $124,600.00. 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.

Accounting & Administrative Coordinator | Venezuela | Hybrid We are looking for an Accounting & Administrative Coordinator to manage end-to-end financial operations and administrative support in Venezuela. This is a key local role with high visibility, responsible for ensuring compliance, handling daily accounting processes, and supporting multiple business areas. What you’ll do: Manage Accounts Payable processes (POs, invoices, payments, accounting entries) Support tax compliance and financial reporting (Venezuela) Coordinate with banks, vendors and payroll providers Provide administrative support across teams Ensure accuracy and control in financial operations We’re looking for: Public Accountant with 3–5 years of experience Strong knowledge of Venezuelan taxes (mandatory) Experience in accounting operations + Excel SAP knowledge is a plus Proactive, autonomous and detail-oriented mindset 📍 Hybrid model (min. 3 days onsite) 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 Cedar Gate Technologies Cedar Gate Technologies, an IQVIA business, enables payers, providers, employers, and service administrators to excel at value-based care with a unified technology and services platform delivering analytics, care, and payment technology on a single data management foundation. At Cedar Gate, you’ll be part of a collaborative, innovative environment where great ideas thrive. We invest deeply in our people through ongoing training, comprehensive benefits, and a strong culture of teamwork, offering the chance to grow your skills while contributing to high impact initiatives for some of the world's most dynamic companies. Position Summary Cedar Gate Technologies, an IQVIA business, is hiring a Director of Data Quality to lead data quality strategies within a complex healthcare data environment, and to modernize data quality processes using Agentic AI and intelligent automation. While this may be an appealing career move for you, we will only consider candidates who can show significant data quality experience in data ecosystems beyond just QA engineering or software QA, and with experience designing and deploying AI agents and agentic workflows at an enterprise level. In this role you will ensure healthcare data is accurate, complete, timely, and fit for operational, regulatory, and analytical use. You will provide leadership across data quality management, governance, reporting integrity, data stewardship, and process improvement. As Director you will partner closely with cross-functional leaders to ensure trusted data supports value-based outcomes, regulatory reporting, and strategic decision-making. In addition, this role serves as a Subject Matter Expert in Agentic AI frameworks and AI-driven data quality capabilities, responsible for advancing the organization’s use of automation and AI to scale and modernize data quality operations. Roles & Responsibilities Data Quality Strategy & Leadership Develop and lead the enterprise-wide Data Quality strategy aligned to business goals and regulatory requirementsEstablish data quality standards, policies, and operating modelsDefine and monitor key dimensions including accuracy, completeness, consistency, timeliness, and integrityImplement data quality scorecards, dashboards, and executive reportingServe as the enterprise leader for data quality practicesAI Agents & Agentic Frameworks Serve as a Subject Matter Expert in Agentic AI frameworks and AI agents, leading the design and implementation of AI-enabled data quality capabilities across the enterprise, including data profiling, anomaly detection, validation, monitoring, root cause analysis, and automated issue triage and remediation recommendationsDefine and operationalize AI use cases within the Data Quality framework, ensuring alignment with business priorities, regulatory requirements, and enterprise risk standardsEstablish and enforce governance standards for AI-driven data quality processes, including human oversight, explainability, and auditability, ensuring responsible and compliant AI adoptionPartner with Data Engineering, AI/ML, and Architecture teams to deploy scalable, production-grade AI-enabled data quality solutions across data platforms and pipelinesData Quality Operations Lead teams responsible for identifying, prioritizing, and resolving data quality issuesEstablish repeatable processes for profiling, root cause analysis, and remediation trackingEmbed data quality controls into data pipelines, platforms, and reporting environmentsLeverage automation and AI to reduce manual effort and improve efficiencyDrive continuous improvement initiatives across data quality processesCross-Functional Collaboration Partner with leaders across Operations, Clinical, Compliance, IT, Analytics, and ProductTranslate business needs into data quality requirements and AI-driven solutionsDrive alignment on data ownership, definitions, and governance practicesCommunicate complex data and AI concepts to executive and non-technical stakeholdersTeam Leadership & Development Lead and develop a high-performing team across data quality, governance, and data operationsEstablish performance metrics, goals, and career development plansBuild capabilities in AI-enabled data quality, automation, and modern data management practicesJob Location Burlington, MA (Boston) Work Arrangement Hybrid (3 days in office, 2 remote)     Experience / Qualifications 10+ years of experience in data quality, data management, data governance, and data operations5+ years of leadership experience managing teams or enterprise data initiativesHands-on experience with AI agents, agentic frameworks, or AI-enabled automationExperience implementing agentic workflows or intelligent automationDemonstrated experience implementing data quality frameworks, controls, and monitoring capabilitiesBachelor’s degree in relevant fields such as Data Management, Computer Science, Healthcare Administration, or Analytics. Master’s degree preferredExperience applying AI to data quality processes such as monitoring, anomaly detection, or remediation for enterprise data operations is highly preferredExperience working with data pipelines, data platforms, or analytics ecosystemsExperience in healthcare payer, healthcare provider, or healthcare technology organizations is preferredKnowledge of healthcare standards (FHIR, HL7, HEDIS, ICD, etc.) will enhance your candidacy.Experience with data governance tools, data quality platforms, or data catalogs will help you be successful in the position.Familiarity with responsible AI practices and AI governance frameworks will reduce your learning curveTo be eligible for this position, you must reside in the same country where the job is located.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 $110,200.00 - $307,200.00. 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.

Únete a nosotros en nuestro emocionante trayecto! IQVIA ™ es The Human Data Science Company ™, enfocada en el uso de datos y ciencia para ayudar a los clientes de la salud a encontrar mejores soluciones para sus pacientes. Formada a partir de la fusión de IMS Health y Quintiles, IQVIA ofrece una amplia gama de soluciones que aprovechan los avances en información, tecnología, análisis e ingenio humano para impulsar la atención médica. Actualmente nos encontramos en la búsqueda de profesionales interesados en ser parte de un gran proyecto con un importante socio de negocios.  Buscamos un profesional apasionado por el marketing digital, con enfoque estratégico y experiencia en la gestión de journeys multicanal dirigidos a profesionales de la salud (HCPs). Serás responsable de: Diseñar, gestionar y optimizar journeys digitales enfocados en la conversión y retención de médicos no visitados.Administrar y mejorar el rendimiento de canales digitales como OCE-D (RTE, MTE, WhatsApp).Coordinar y ejecutar eventos virtuales a través de On24.Diseñar e implementar campañas en redes sociales para ampliar el alcance con HCPs.Proponer, implementar y optimizar campañas basadas en datos de terceros (3rd Party Data).Analizar resultados y generar insights para la mejora continua de las estrategias multicanal.Requisitos: Licenciatura en Marketing, Comunicación, Publicidad, Ciencias de la Salud o afín.Experiencia comprobable en marketing digital multicanal, idealmente en la industria farmacéutica o de salud.Conocimiento avanzado en plataformas como OCE-D, On24, Meta Ads, Google Ads, y herramientas de automatización.Capacidad analítica para interpretar datos y optimizar campañas.Inglés avanzado indispensable (comunicación con equipos globales).#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.

Job OverviewPerform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.Essential Functions• Provide clinical research support to investigators and site staff, including• Verify and/or correct research study information on source documents; research queries and variances; and providefeedback to the site data collector.• Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content,accuracy, and completeness.• Prepare and maintain research study files. Compile, collate and submit study information within established deadlines.• Collect and submit regulatory/ethics documentation pertaining to the research study.• Maintain the FDA 1572 form for assigned research studies.• Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits.• Input visit data into clinical trial management system (CTMS) to track patient visits and procedures completed against the study budget.Qualifications• Bachelor degree• Educational equivalent and 2 years’ relevant work experience in a clinical environment or medical setting; or equivalent combination of education, training and experience Req• Basic knowledge of clinical trials• In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and studyschedules• Basic knowledge of medical terminology• Basic skill in using MS Windows and Office applications such as Access, Outlook, Excel, and Word• Excellent interpersonal skills• Ability to pay close attention to detail• 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 OverviewPerform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.Essential Functions• Provide clinical research support to investigators and site staff, including• Verify and/or correct research study information on source documents; research queries and variances; and providefeedback to the site data collector.• Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content,accuracy, and completeness.• Prepare and maintain research study files. Compile, collate and submit study information within established deadlines.• Collect and submit regulatory/ethics documentation pertaining to the research study.• Maintain the FDA 1572 form for assigned research studies.• Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits.• Input visit data into clinical trial management system (CTMS) to track patient visits and procedures completed against the study budget.Qualifications• Bachelor degree• Educational equivalent and 2 years’ relevant work experience in a clinical environment or medical setting; or equivalent combination of education, training and experience Req• Basic knowledge of clinical trials• In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and studyschedules• Basic knowledge of medical terminology• Basic skill in using MS Windows and Office applications such as Access, Outlook, Excel, and Word• Excellent interpersonal skills• Ability to pay close attention to detail• 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.

Clinical Research Associate IQVIA Belgium is looking for talented and motivated experienced CRA to join our Site Management team. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization. Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Your responsibilities will include: Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesWork with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.• Collaborate and liaise with study team members for project execution support as appropriate.If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.Your Profile University degree in scientific discipline or health care2+ years of experience as a CRAVery good computer skills including MS OfficeExcellent command of Dutch, French and English language. Belgium based.Organizational, time management and problem-solving skillsAbility to establish and maintain effective working relationships with coworkers, managers, and clientsFlexibility to travelDriver’s license class BWhat you can expect:  Resources that promote your career growthLeaders that support flexible work schedulesPrograms to help you build your therapeutic knowledgeExcellent working environment in a stabile, international, reputable companyCompany car, mobile phone and attractive benefits packagingIQVIA 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.

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 86.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Komm in unser IQVIA-Team! Für ein spannendes Projekt im Bereich Impfstoffe suchen wir Pharmaberater (m/w/d) zum nächstmöglichen Zeitpunkt Im Gebiet: Celle, Braunschweig, Hildesheim, Goslar, Wolfsburg Das sind Deine Aufgaben: Durch die intensive Betreuung ausgewählter Ärzte förderst Du die Verordnung Deiner Präparate und trägst so maßgeblich zum Unternehmenserfolg bei. Du setzt als Experte auf der Basis Deines Fachwissens Beratungsstrategien erfolgreich um und überzeugst so Deine Ansprechpartner. Du findest mit Deinen Gesprächspartnern innovative Therapiekonzepte in anspruchsvollen Indikationen. (optional: zum Wohle des Patienten/für den Patienten/und trägst somit zur Gesundheit und dem Patientenwohl bei) Du führst regionale und zentrale Fortbildungsveranstaltungen in enger Abstimmung mit dem Regionalleiter und Deinem regionalen Team durch. Das bringst Du mit: Du hast bereits Erfahrung als Pharmaberater, Pharmareferent oder Klinikreferent in verschiedenen Indikationen gesammelt. Du verfügst über eine Naturwissenschaftliche Ausbildung (idealerweise Hochschulabschluss) oder Ausbildung zum Geprüften Pharmareferent (m/w/d) gemäß §75 AMG Als durchsetzungsstarke Persönlichkeit und erfahrener Netzwerker verstehst Du es, dich und Deine Ansprechpartner zu begeistern. Du möchtest etwas bewegen – für Dein Präparat, für dich selbst und vor allem für betroffene Patienten. Ausgeprägte kommunikative Fähigkeiten sowie die Bereitschaft, eigenverantwortlich und ergebnisorientiert zu arbeiten. Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] #LI-CES #LI-DNP #LI-SS2 #Pharmaberater #Biologie #Chemie #Pharmareferent #BTA #CTA #PTA #Oecotrophologie #Pharmazie #Pharma-Außendienst 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.

E-Commerce & Performance Marketing ManagerLocation: Bournemouth, DorsetContract: 12-month FTC (Maternity Cover) Job Overview: Drives revenue growth for complex, full-service product offerings on Amazon by aligning marketing strategies with broader business objectives. Leverages Amazon-specific tools and data insights (e.g., Vendor/Seller Central, advertising platforms, AMC and analytics) to effectively engage diverse customer segments and optimise campaign performance. Consistently delivers against sales and ROI targets by collaborating with cross-functional teams and leading coordinated marketing initiatives. Identifies and scales high-potential opportunities through keyword optimisation, content enhancement, and promotional strategies, contributing to increased visibility, conversion, and new business growth on the platform. Essential functions: Develop and execute a dynamic Amazon-first digital strategy across Seller/Vendor Central, performance marketing (Amazon Ads) and to drive sales growth, visibility and conversion rate improvements.· Own and optimise all Amazon marketing channels (Sponsored Products, Sponsored Brands, Sponsored Display & DSP), ensuring ROAS, TACoS and CAC targets are consistently achieved through structured testing and optimisation.Oversee Amazon listing optimisation, including keyword strategy, SEO, A+ Content, Brand Stores and conversion rate improvements.Drive ongoing development of the Amazon tech stack and data ecosystem, including reporting tools, AI-driven insights, keyword harvesting, and full funnel attribution across Amazon Ads and external traffic.Lead, mentor and develop the Performance Marketing team, ensuring best-in-class execution across Amazon advertising and marketplace management.  Ensure the team delivers high-quality Amazon content, including optimised PDPs, enhanced brand content and creative aligned with marketplace best practice.Create and execute full-funnel Amazon advertising strategies across AMS (Sponsored Ads), Amazon DSP, and Prime Video, driving awareness, consideration, and conversion through integrated, data-led campaign planning and optimisation.Own and deliver Amazon sales and performance reporting translating data into actionable insights for clients.Advise clients on navigating Amazon’s ecosystem, including catalogue setup, compliance, retail readiness, inventory planning and scaling strategies for a full-funnel Amazon growth approach.Be responsible for any other reasonable tasks in relation to the overall role as required.What we’re looking for Minimum of 2 years in similar role managing Amazon AdsConfident with data, reporting and ExcelOrganised, proactive and commercially focusedStrong communication and stakeholder management skillsWhy join us Fast paced, collaborative environmentOpportunity to shape strategy and make an impactExposure to AI, analytics and innovative toolsIf you enjoy combining data, creativity and commercial results, apply now and join a growing digital team. Please note applicants must have the right to work in the UK. 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.

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.• Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.• Assist with periodic review of study files for completeness.• Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.• Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.• May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training. Qualifications• Bachelor Degree in Life Science or Healthcare.• 1-2 years administrative support experience or an Intern experience in clinical research or pharma. • Availability to go to the office: Hybrid position. • Location: Bogota, Colombia • Written and verbal communication skills including good command of English language.• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.• Effective time management and organizational skills.• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.• Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.• Knowledge of applicable protocol requirements as provided in company training. 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 OverviewThis is a great opportunity for an experienced Senior QA Analyst  join a global leader to work across a variety of projects. This is an ideal position for a QA Analyst with experience in complex software development project(s) in a commercial environment. You will have strong interpersonal skills and the ability to work with a wide range of people, from Architects, Big Data Engineers, QA Engineers, Front End Developers, through to the stakeholder team.Under broad guidance, executes and verifies software applications tests. Essential Functions• Understands and reviews requirements, creates test plans and/or contributes in test estimations, manual and automation planning/strategies.• Responsible for test case planning, authoring and execution of compliance products’ for client implementation projects.• Performs test iterations, defect tracking and reports test results; troubleshoots and coordinates with team focusing on defect resolution.• Collaborates with Developers, Tech Leads/Managers, BAs/Consultants and other project stakeholders throughout the SDLC.• Coordinates with BAs and development teams in troubleshooting and resolving road blocks and issues.• Regularly documents, tracks and escalates issues and feedback as appropriate.• Experience in running manual and automated test scripts and identifying scope for areas for automation.• Proactively seeks necessary managerial support to discuss/flag risks and mitigation plans• Typically requires 3-5 years of prior relevant experience Qualifications• Bachelor's Degree  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 OverviewThis is a great opportunity for an experienced Senior QA Analyst  join a global leader to work across a variety of projects. This is an ideal position for a QA Analyst with experience in complex software development project(s) in a commercial environment. You will have strong interpersonal skills and the ability to work with a wide range of people, from Architects, Big Data Engineers, QA Engineers, Front End Developers, through to the stakeholder team.Under broad guidance, executes and verifies software applications tests. Essential Functions• Understands and reviews requirements, creates test plans and/or contributes in test estimations, manual and automation planning/strategies.• Responsible for test case planning, authoring and execution of compliance products’ for client implementation projects.• Performs test iterations, defect tracking and reports test results; troubleshoots and coordinates with team focusing on defect resolution.• Collaborates with Developers, Tech Leads/Managers, BAs/Consultants and other project stakeholders throughout the SDLC.• Coordinates with BAs and development teams in troubleshooting and resolving road blocks and issues.• Regularly documents, tracks and escalates issues and feedback as appropriate.• Experience in running manual and automated test scripts and identifying scope for areas for automation.• Proactively seeks necessary managerial support to discuss/flag risks and mitigation plans• Typically requires 3-5 years of prior relevant experience Qualifications• Bachelor's Degree  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 Summary  The Medical Laboratory Scientist performs high‑complexity clinical laboratory testing to support patient care and clinical research activities. This role applies professional and technical expertise to generate accurate, timely, and reliable laboratory results in areas such as hematology, chemistry, immunology, and specialized testing. Work is performed in accordance with CLIA regulations, CAP standards, Good Clinical Laboratory Practice (GCLP), and applicable quality and safety requirements.  Essential Duties and Responsibilities Performs and reports high‑complexity laboratory tests, both automated and manual, with minimal supervision. Demonstrates competency in laboratory principles, methodologies, and instrumentation across assigned testing areas. Maintains adequate inventory of reagents and supplies and prepares reagents as required. Identifies and reports irregularities, instrument issues, or factors that may affect test accuracy. Participates in assay validation, method improvements, and implementation of new technologies. Follows all safety procedures, uses required personal protective equipment, and reports safety concerns. Ensures compliance with CLIA, CAP, GCLP, and internal quality management systems. Adheres to quality control policies, documents QC activities, and maintains a clean, organized work environment. Maintains required training, competency assessments, and continuing education. Supports internal and external audits, inspections, and quality initiatives. Verifies quality control results and releases patient or study results in accordance with regulatory requirements. Assists with training and onboarding of laboratory personnel as needed. Performs duties in alignment with ICH E6 Good Clinical Practice guidelines when supporting clinical trials. Participates in special projects and performs additional tasks assigned by laboratory leadership.  Required Education and Experience Bachelor’s degree in Medical Laboratory Science, Biology, Chemistry, or a related field. 0–5 years of clinical laboratory experience. Meets CLIA requirements for high‑complexity testing personnel. National certification as MLS/MT (ASCP, AMT, or equivalent) required. Strong understanding of laboratory principles, testing methodologies, and regulatory standards. Proficiency in laboratory safety, infection control, and handling of hazardous chemicals. Ability to perform complex calculations, including averages, standard deviations, and QC metrics. Skilled in troubleshooting laboratory instruments and resolving testing issues. Proficient with Microsoft Excel, Word, and PowerPoint. Strong organizational, interpersonal, and communication skills. Ability to manage multiple tasks with accuracy and attention to detail. Ability to work effectively with colleagues, management, and external partners.  Why Join Us? At NEXT Oncology (an Avacare Business), you’ll be part of a mission-driven team that values collaboration, precision, and patient safety. Our team is known for its supportive culture, strong communication, and commitment to excellence in clinical research. 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 $46,200.00 - $96,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also consider CRA 1 candidates with a minimum of 6 months on-site monitoring experience. Must have experience monitoring in oncology solid tumor. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. Job OverviewWe are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to the integrity and quality of clinical research data. Key Responsibilities Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines. Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals. Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues. Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity. Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries. Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards. Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence. Work closely with cross-functional project teams to support study execution and ensure alignment with project goals. Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking. Qualifications Bachelor’s degree in life sciences or health-related field (or equivalent experience). Requires at least 1 year of on-site monitoring experience. Strong understanding of GCP, ICH guidelines, and regulatory requirements. Ability to travel as required by the project. 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 $71,900.00 - $169,300.00. 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.

 Description of Roles and Responsibilities This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, Sponsor policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the SCOM or CRD, the person is responsible for budget/finance aspects, for execution and oversight of clinical trial country submissions and approvals and to ensure Site Ready. Responsibilities include but are not limited to: Ownership of country and site budgets. Development, negotiation, and completion of Clinical Trial Research Agreements (CTRA). Oversees and tracks clinical research-related payments. Payment reconciliation at study close-out. Oversees FCPA, DPS/OFAC, and maintenance of financial systems. Experience Required • 5-7 years of experience in clinical research or combined experience in Clinical Research and Finance/BusinessFinancial forecasting in conjunction with SCOM /CRDs, other roles.Executes and oversees clinical trial country submissions and approvals for assigned protocols.Develops local language materials including local language Informed Consents and translations. Interacts with IRB/IEC and Regulatory Authority for assigned protocols.Manages country deliverables, timelines, and results for assigned protocols to meet country commitments. Responsible for quality and compliance in assigned protocols in country.Contributes to the development of local SOPs. Oversees CTCs as applicable.Coordinates and liaises with CRM, CTC, CRA, (Finance and Legal if appropriate) to ensure country deliverables are obtained for submissions, budgets, CTRAs and local milestones.Collaborates closely with Headquarter to align country timelines for assigned protocols.Provides support and oversight to local vendors as applicable.Oversees and coordinates local processes, clinical and ancillary supplies management, importing and exporting requirements, supplies destruction, local electronic/hard copy filing, archiving and retention requirements, and insurance process management. Enters and updates country information in clinical and finance systems.Ownership of local regulatory and financial compliance. The position has a significant impact on how a country can deliver country-specific trial commitments and objectives especially during study start-up.Required to in/directly influence investigators, external partners and country operations to adheres to budget targets and agreed payment timelines.Works in partnership internally with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and sites, IRB/IECs and Regulatory Authorities in submission and approval related interactions. Through continual interaction with local clinical team/s successfully delivers clinical and financial contracts within fair market value.Contribute or lead initiatives and projects adding value to the businessContributes strongly to COM team and other Country Operations roles knowledge by acting as process Subject Matter Expert (SME), sharing best practices, making recommendations for continuous improvement, and providing training as appropriate/required.Contributes to COM team knowledge by acting as buddy/mentor and sharing best practices as appropriate/required Experience Required5-7 years of experience in clinical research or combined experience in Clinical Research and Finance/Business In today’s world, continuing to grow and expand your skills is as important as ever. Discover career possibilities and chart your own path at IQVIA. The potential base pay range for this role, when annualized, is 34, 400 EUR - 66, 200 EUR. 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. Employee Referral Payment Standard Referral Bonus Plan 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.

Wil jij bijdragen aan betere toegang tot innovatieve zorg in Nederland? Voor ons Health Technology Assessment (HTA) & Market Access team zoeken wij een Nederlandstalige Associate Consultant (analist) met achtergrond in gezondheidswetenschappen, epidemiologie, (gezondheids)economie, wiskunde of statistiek. Je werkt in een multidisciplinair team vanuit Amsterdam en ondersteunt farmaceutische en MedTech organisaties, zorginstellingen en overheden (zoals Zorginstituut Nederland) bij het verbeteren van zorgkwaliteit en -toegang. RolJe draagt bij aan de ontwikkeling en uitvoering van vergoedingsdossiers en markttoegangsstrategieën, in nauwe samenwerking met nationale en internationale teams. VerantwoordelijkhedenOpstellen van HTA- en gezondheidseconomische analyses en dossiersUitvoeren van kwantitatief en kwalitatief onderzoek en modelleringAdviseren over prijsstelling, vergoeding en markttoegangBeheren van projectplanningen en klantcontactAnalyseren en rapporteren van gezondheidsdataSchrijven van wetenschappelijke rapporten en presentatiesDeelnemen aan klant- en stakeholdermeetings (o.a. Zorginstituut)Signaleren van nieuwe businesskansenToepassen van AI-ondersteunde werkwijzenProfielMaster in relevant vakgebied1–3 jaar ervaring (bij voorkeur met wetenschappelijk schrijven)Sterke analytische en kwantitatieve skills (Excel, R/Stata)Goede communicatieve vaardigheden en klantgerichtIn staat complexe materie helder te vertalen naar het NederlandsVloeiend Nederlands en sterk EngelsWat biedt IQVIA?Werk met maatschappelijke impactPersoonlijke ontwikkeling en doorgroeimogelijkhedenDynamische, internationale werkomgevingFlexibel werken (Amsterdam + deels thuis + klantlocaties)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.

Wil jij impact maken op de toegang tot innovatieve zorg in Nederland? Voor ons HTA & Market Access team zoeken wij een Senior Consultant / Associate Director (afhankelijk van ervaring) met aantoonbare expertise in gezondheidseconomie, HTA en/of Market Access binnen Nederland. Je hebt ervaring met het opstellen en indienen van vergoedingsdossiers bij o.a. Zorginstituut Nederland en Zorgverzekeraars Nederland en bent vloeiend in Nederlands en Engels. RolAls senior expert ben je het aanspreekpunt voor klanten en eindverantwoordelijk voor de kwaliteit van vergoedingsdossiers. Je combineert inhoudelijk leiderschap met projectmanagement en draagt bij aan de groei van het team en de business. VerantwoordelijkhedenLeiding nemen in HTA- en Market Access-projectenOntwikkelen en reviewen van vergoedingsdossiersAdviseren over prijs-, vergoedings- en markttoegangsstrategieënCoördineren van projecten en bewaken van kwaliteit en deadlinesAansturen en coachen van consultantsVolgen van (inter)nationale ontwikkelingen in het veldOnderhouden van klantrelaties en fungeren als inhoudelijk sparringpartnerBijdragen aan business development (±20–30%)Profiel3–10 jaar ervaring in HTA/Market Access (industrie of consultancy)Diepgaande kennis van het Nederlandse zorg- en vergoedingssysteemMaster in biomedische wetenschappen, gezondheidseconomie, farmacie of vergelijkbaarSterke analytische, communicatieve en presentatievaardighedenErvaring met stakeholdermanagement en projectleidingVloeiend Nederlands en uitstekend EngelsWat biedt IQVIA?Impactvolle rol in toegang tot innovatieve behandelingenSleutelpositie in groeiende afdelingRuimte voor persoonlijke en professionele ontwikkelingSamenwerking met diverse stakeholders en expertteamsFlexibel werken (Amsterdam, deels thuis, reizen binnen NL)Sterke teamcultuur en dynamische werkomgevingIQVIA 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.

Do naszego zespołu poszukujemy osoby na stanowisko Marketing Specialist, która będzie odpowiadać za realizację i koordynację projektów marketingowych dla klientów z branży farmaceutycznej. Stanowisko jest zlokalizowane w Warszawie, praca w trybie hybrydowym 1 raz w tygodniu w biurze. Zakres obowiązków: Koordynacja i realizacja projektów digital marketing Współpraca z klientami z branży pharma – bieżąca komunikacja, zbieranie potrzeb, rekomendowanie rozwiązań Zarządzanie projektami oraz harmonogramami działań Ścisła współpraca międzydziałowa (IT, graficy, sprzedaż) Tworzenie i rozwój koncepcji marketingowych oraz kampanii digital Rozwój i promocja produktów wewnętrznych Przygotowywanie briefów oraz precyzyjnych wytycznych dla zespołów projektowych Monitorowanie postępów projektów i dbanie o ich terminową realizację Wymagania: Doświadczenie w marketingu (mile widziane w branży pharma lub pokrewnej) Wykształcenie wyższe farmaceutyczne Doświadczenie w pracy projektowej / agencyjnej będzie dużym atutem Bardzo dobra organizacja pracy własnej i zarządzania czasem Wysokie umiejętności komunikacyjne i kultura pracy z klientem Kreatywność oraz nastawienie na rozwiązywanie problemów Umiejętność pracy zespołowej i współpracy międzydziałowej Umiejętność formułowania jasnych, precyzyjnych wytycznych Zmysł estetyczny oraz rozumienie standardów komunikacji marketingowej Mile widziana znajomość narzędzi do zarządzania projektami (np. ClickUp) Dodatkowe atuty: Doświadczenie w projektach digital (kampanie, strony, platformy) Znajomość podstaw UX/UI lub marketing automation Umiejętność pracy na danych i wyciągania wniosków (analityczne podejście) Oferujemy: Pracę przy projektach dla dużych, międzynarodowych klientów z branży farmaceutycznej Możliwość rozwoju kompetencji w obszarze marketingu cyfrowego i pharma marketingu Realny wpływ na rozwój produktów i projektów Pracę w dynamicznym, interdyscyplinarnym zespole Przyjazną atmosferę oraz kulturę współpracy 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 potential base pay range for this role, when annualized, is 99 400,00 zł - 184 500,00 zł. 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.

Professional OverviewExperienced Clinical Data Management professional with proven expertise in leading end-to-end delivery of data management services across single and multi-service clinical projects. Adept at ensuring high-quality deliverables are completed on time, within budget, and in full compliance with GCP, regulatory requirements, and SOPs. Strong background in acting as a Data Team Lead (DTL), driving project planning, execution, and close-out while fostering collaboration across cross-functional teams. Recognized for delivering customer-focused solutions, managing stakeholder relationships, and implementing continuous process improvements. Key Responsibilities & ExpertiseClient & Stakeholder ManagementAct as the primary point of contact for clients on all data management deliverablesBuild and maintain strong, long-term customer relationshipsCollaborate with client data managers, stakeholders, and internal teams to ensure seamless project executionLead discussions on timelines, resourcing, deliverables, and process improvementsManage escalations effectively, ensuring timely resolution of issuesProject & Service DeliveryLead full data management lifecycle from study start-up to close-outProvide technical and operational leadership across DM projectsEnsure milestones, deliverables, and timelines are consistently metServe as escalation point for complex or unresolved data issuesCoordinate closely with Data Operations teams, functional leads, and project managersOversee development, review, and approval of Data Management Plans (DMPs)Implement proactive quality management strategies and drive continuous improvementQuality & ComplianceEnsure all processes are aligned with Good Clinical Practice (GCP) and regulatory guidelinesMonitor quality metrics and identify root causes of issuesLead corrective and preventive actions (CAPA) where neededMaintain compliance with SOPs, policies, and internal systemsFinancial & Operational OversightManage project budgets and Scope of Work (SOW) deliverablesReview financial performance and contribute to project forecastingIdentify and manage out-of-scope activities and change ordersSupport revenue tracking, invoicing, and financial reportingContribute to RFP responses, pricing strategies, and bid defense meetingsLeadership & Continuous ImprovementProvide leadership and mentorship to data management teamsPromote efficient workflows and high-quality standardsContribute to process optimization and implementation of new technologiesParticipate in global and local best practice initiativesCore CompetenciesClinical Data Management Lifecycle (Phase I–III, especially Phase III)Data Team Leadership (DTL)Project Management & DeliveryStakeholder & Client ManagementDatabase & Data Quality OversightSAE & External Vendor ReconciliationGCP & Regulatory ComplianceCross-functional Team LeadershipFinancial & Resource ManagementProcess Improvement & InnovationQualificationsBachelor’s degree in Health, Clinical, Biological, Mathematical Sciences or related field≥3 years Clinical Data Management experience≥1 year experience as Project Lead / Data Team LeadProven delivery of at least one Phase III clinical studyStrong knowledge of:Medical terminology, pharmacology, anatomy, physiologyData management systems and processesRegulatory requirements and GCPProfessional StrengthsExcellent communication, interpersonal, and customer engagement skillsStrong analytical and problem-solving abilityHighly organized with strong attention to detailAbility to work independently with minimal supervisionProven ability to build and maintain collaborative relationshipsIQVIA 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 potential base pay range for this role, when annualized, is zł157,400.00 - zł394,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 86.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für ein spannendes Projekt im Bereich Diabetes suchen wir Pharmareferenten als Portfolio-Spezialist Diabetes & Adipositas (m/w/d) Im Gebiet: Neu-Ulm, Günzburg, Landsberg, Königsbrunn Das sind Deine Aufgaben: Als Portfolio Spezialist (m/w/d) bist du dafür zuständig, fundierte Informationen zu deinem Produktportfolio im Bereich metabolischer Erkrankungen sowie den Dienstleistungen professionell zu vermitteln. Dabei übernimmst du innerhalb deines zugewiesenen Gebiets, der Produktsparte oder für ausgewählte Kunden im Bereich niedergelassener Allgemein- und Fachärzte eine Vielzahl spannender Aufgaben: Eigenständige Planung, Durchführung und Analyse von Kundenkontakten sowie Erstellung eines gebietsspezifischen Aktivitätenplans. Umsetzung der nationalen Sales- und Marketingstrategie und Aufbau nachhaltiger Beziehungen zu Zielkunden. Verantwortung für den wirtschaftlichen Erfolg der Fokusprodukte und die Organisation regionaler Fortbildungen (Präsenz & Digital). Aktive Mitwirkung an Tagungen, Meetings und Awareness-Kampagnen, um Innovationen und Pipeline-Produkte zu fördern. Sorgfältige Dokumentation aller Aktivitäten im CRM-System und kontinuierliche Weiterbildung durch interne und externe Trainings. Das bringst Du mit: Du bist geprüfter Pharmareferent (m/w/d), Pharmaberater (m/w/d) oder bringst eine vergleichbare Qualifikation gem. §75 AMG mit (z. B. durch ein naturwissenschaftliches Studium). Erfahrung im Pharma- oder Medizintechnikvertrieb wünschenswert. Interesse an neuen innovativen Produkten und deren Platzierung im Markt. Ausgeprägte Kommunikationsstärke im Umgang mit unterschiedlichen Zielgruppen sowie eine klare wirtschaftliche Ziel- und Kundenorientierung. Du möchtest etwas bewegen – für Dein Präparat, für dich selbst und vor allem für betroffene Patienten. Ausgeprägte soziale Kompetenz und Teamfähigkeit. Sehr gute kommunikative Fähigkeiten sowie die Bereitschaft, eigenverantwortlich und ergebnisorientiert zu arbeiten. Du verfügst über ein ausgeprägtes digitales Know-how gepaart mit IT-Kompetenz. Fließende Deutschkenntnisse in Wort und Schrift sind Voraussetzung. Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] #LI-CES #LI-DNP #LI-SS2 #Pharmaberater #Biologie #Chemie #Pharmareferent #BTA #CTA #PTA #Oecotrophologie #Pharmazie #Pharma-Außendienst 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.

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 86.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für unseren Kunden, ein renommiertes, international agierendes Familienunternehmen, suchen wir zum nächstmöglichen Zeitpunkt einen Pharmaberater (m/w/d) General Medicine / Diabetes Im Gebiet: Tübingen, Böblingen, Rottenburg a. N Das sind Deine Aufgaben: Durch die intensive Betreuung ausgewählter Ärzte förderst Du die Verordnung Deiner Präparate und trägst so maßgeblich zum Unternehmenserfolg bei. Du setzt als Experte auf der Basis Deines Fachwissens Beratungsstrategien erfolgreich um und überzeugst so Deine Ansprechpartner. Du findest mit Deinen Gesprächspartnern innovative Therapiekonzepte in anspruchsvollen Indikationen. (optional: zum Wohle des Patienten/für den Patienten/und trägst somit zur Gesundheit und dem Patientenwohl bei) Du führst regionale und zentrale Fortbildungsveranstaltungen in enger Abstimmung mit dem Regionalleiter und Deinem regionalen Team durch. Das bringst Du mit: Du hast idealerweise bereits erste Erfahrung im Pharma-Außendienst gesammelt, idealerweise in der Indikation Diabetes. Als durchsetzungsstarke Persönlichkeit und erfahrener Netzwerker verstehst Du es, Dich und Deine Ansprechpartner zu begeistern. Du möchtest etwas bewegen – für Dein Präparat, für Dich selbst und vor allem für betroffene Patienten. Ausgeprägte kommunikative Fähigkeiten sowie die Bereitschaft, eigenverantwortlich und ergebnisorientiert zu arbeiten. Du kannst mit digitalen Medien gut umgehen und hast solide Kenntnisse, um auch englische Fachtexte zu verstehen. Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] #LI-CES #LI-DNP #LI-SS2 #Pharmaberater; #Biologie; #Chemie; #Pharmareferent; #BTA; #CTA; #PTA; #Oecotrophologie; #Pharmazie; #Pharma-Außendienst 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.