IQVIA

Möchten Sie Ihre Erfahrung in der klinischen Forschung gezielt in einer Teilzeitrolle einsetzen? Arbeiten Sie gerne patientennah und strukturiert und legen Wert auf feste Einsatztage? Zur Unterstützung einer laufenden klinischen Studie suchen wir ab sofort eine erfahrene:n Studienkoordinator:in / Clinical Research Coordinator / Study Nurse (m/w/d) für ein Studienzentrum in Trier. RahmenbedingungenArbeitszeit: 16 Stunden pro WocheEinsatztage: Montag und DienstagVertragsdauer: ca. 6 MonateStart: kurzfristig möglichIhre AufgabenIn dieser Rolle übernehmen Sie eine zentrale Funktion im Studienalltag und arbeiten eng mit dem Prüfarztteam zusammen: Koordination und Betreuung einer klinischen Studie unter Delegation des Principal InvestigatorsSicherstellung des Wohlergehens der Patient:innen sowie professionelles Patienten‑ und BesuchsmanagementPlanung, Durchführung und Nachbereitung von StudienvisitenPflege und Dokumentation von Studiendaten in EDC‑Systemen sowie in CRFsDateneingabe, Datenprüfung und Bearbeitung von QueriesOrganisation studienspezifischer Abläufe und logistischer Prozesse gemäß ProtokollUnterstützung bei Rekrutierung, Screening und Einschluss von Patient:innenZusammenarbeit mit Monitor:innen und Beantwortung studienbezogener RückfragenNice to have (keine Voraussetzung): Erfahrung mit Blutentnahmen und EKGsIhr ProfilMindestens 2 Jahre Erfahrung in der klinischen Forschung (z. B. als Study Nurse, CRC, Studienkoordinator:in)Sehr gute Kenntnisse im Daten‑ und Visit‑Management klinischer StudienSicherer Umgang mit EDC‑SystemenStrukturierte, zuverlässige und patientenorientierte ArbeitsweiseSehr gute Deutschkenntnisse in Wort und SchriftGute IT‑Kenntnisse (MS Office)#LI-CES #LI-XS #LI-HCPN #LI-DNP 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.

Roles and Responsibilities Under close guidance or supervision, responsible for creating and maintaining the IMS database.Will be part of the Phoenix Parallel team.Implements database setups of development, user acceptance test, and production environmentsParticipates in database analysis and database design tasks to meet required operational standards and performance levelsOptimizes queries, stored procedures, etc. for high throughput, availability, scalability, redundancy, superior performance and quick recoverabilityMonitors, manages, and supports multiple local and remote SQL server instances on Windows boxesResolves production related issues and requests, and clarifies issues with relevant production teams Interacts with production teams to update details of all production related binding documentsParticipate in data supplier calls to monitor the status of data issues and ensure follow ups are done and progress is being tracked. Monitors data loading jobs across different IQVIA systemsAssures the accuracy and timeliness of additions and modifications to the IMS sales databases through input from internal and external sources, while understanding the impact of data trends and on all stakeholders.Identifies assigned supplier and database exceptions through Quality Control review and/or maintenance within the file and resolves data issues.Ensures all maintenance performed rules and protocols.Makes daily verification supplier processing and output and applies corrections as needed.Assures that decisions made follow the protocols. Visually monitors data for any trends in the weekly client information.Maintains documentation of Quality Control Procedures.  List of required skills for this role: Bachelor’s /College Degree in Computer Science, Information Technology, Mathematics, Statistics, Actuarial Science, Business, Communication or equivalent preferredMinimum of 2 years relevant work experience preferred Proficient in Windows applications (Excel, Word, Access, PowerPoint, etc.).Basic SQL skills is preferred.Excellent written and oral communication skillsCan effectively communicate with various levels of the organizationStrong ability to deal tactfully with internal and external clients through emails or callsExcellent organizational and time management skills are required Demonstrate strong problem solving and analytical skills, can process and understand large amounts of data to isolate issue in question, identify patterns and trends in data setsExperience working in a mainframe environment preferred. Knowledge and understanding of the pharmaceutical industry is a plus.Knowledge and relevant background on IQVIA syndicated sales and prescription data, and in-depth understanding of the US pharmaceutical industry and market dynamics is a plusTime Management skills and ability to work independently. Ability to resolve basic problems pertaining to database issues.Ability to identify/eliminate repetitive problems and standardize the processes by using existing research tools.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 OverviewPrepares and/or reviews regulatory submissions to support clinical trial and marketing authorisation activities for either internal and/or external clients.  Independently provides regulatory support for more complex projects. Essential Functions Acts as a Regulatory Team Leader on complex projects, which may include technical writing and/or may act as a Project Manager for a stand-alone project, with guidance from senior staff as appropriate. Competently writes regulatory and/or technical documents with minimal review by senior staff. Establishes relationships with many customers; may meet face to face without rest of team to discuss regulatory issues and present lessons learned.  Adopts a proactive and flexible approach to resolve any issues. Undertakes detailed review and management of budgets related to projects, including out of scope activities. Ensures revenue is recognised and challenges when appropriate, may seek guidance from senior staff as appropriate. May give guidance to junior colleagues, including feedback on the quality of technical documents, and may assist in their training and development. May present to clients at bid defence meetings by phone or in person, for a range of regulatory deliverables, at discretion of senior staff. May write new regulatory SOPs, and/or propose revisions and/or act as reviewer for regulatory SOPs, as assigned and appropriate. May be involved in a Regulatory and/or IQVIA Initiative. Performs other tasks or assignments, as delegated by Regulatory management. Qualifications Bachelor's Degree in Life science or related discipline Master's Degree in Life science or related discipline Demonstrates comprehensive regulatory or technical area of expertise Good negotiating skills and the ability to identify and resolve issues, using flexible adaptable approach Strong software and computer skills, including MS Office applications Demonstrated skills in chairing small meetings Ability to work on several projects, retaining quality and timelines and can prioritise workload with minimal supervision Ability to propose revisions to SOPs or suggest process improvements for consideration 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.

Principais Atribuições:•    Postura de Senior: Ownership sobre entregas, atuar como referência técnica, capacidade de sugerir soluções de dados com autonomia.•    Análise exploratória de dados (EDA) e construção de relatórios para geração de insights para áreas da força de vendas.•    Criação de dashboards e relatórios automatizados. Soft Skills:•    Pensamento analítico e crítico – capacidade de entender problemas complexos e propor soluções baseadas em dados.•    Comunicação clara e objetiva – para traduzir análises técnicas em linguagem acessível ao negócio.•    Proatividade – Sugestão de melhorias nos processos de forma independente.•    Adaptabilidade – para lidar com mudanças rápidas e novas tecnologias. Hard Skills:•    SQL avançado – manipulação, modelagem e otimização de queries.•    EDA (Exploratory Data Analysis) – capacidade de investigar e interpretar dados de forma crítica.•    DataViz: Conhecimento em ferramentas de visualização como Power BI. Diferenciais desejáveis:•   Conhecimento das Auditorias (MDTR, DDD, GPS, FMB&NRC, EEP); • Graduação em TI, Ciência de Dados, Engenharia, Estatística ou áreas correlatas. A IQVIA está empenhada em adotar um ambiente de trabalho diverso e inclusivo. Nosso objetivo é atrair e reter as melhores pessoas, independentemente de gênero, raça, estado civil, origem étnica, nacionalidade, idade, deficiência, orientação sexual, identidade de gênero ou qualquer outra característica. Junte-se a nós! #LI-CES #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewManage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives. Essential Functions• Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work, assessing performance and guiding professional development, rewarding and disciplining employees, and addressing employee relations issues and resolving problems.• Participate in the selection for hiring new employees by conducting candidate review and participating in the interviewing process. Ensure that new employees are properly onboarded and trained.• Ensure that staff has the proper materials, systems access and training to complete job responsibilities. Provide oversight for the execution of the training plan, SOP review and training experiences, as applicable.• Participate in the allocation of resources to clinical research projects by assigning staff to clinical studies based on their experience and training.• Manage the quality of assigned staff's clinical work through regular review and evaluation of work product.• Identifies quality risks and issues and create appropriate corrective action plans to prevent or correct deficiencies in performance of staff.• Ensures that staff are meeting defined workload and quality metrics through regular review and reporting of findings as outlined by clinical operations management.• May collaborate with other clinical teams and other functional leadership to manage project related challenges and to achieve exemplary customer service.• Participates in corporate or organizational departmental quality or process improvement initiatives. Qualifications• Bachelor's Degree Degree in scientific discipline or health care preferred. Pref• Prior clinical trial experience including experience in a management/leadership capacity or equivalent combination of education, training and experience.• In-depth knowledge of applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).• Good leadership skills.• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.• Written and verbal communication skills including good command of English.• Excellent organizational and problem solving skills.• Effective time management skills and ability to manage competing priorities.• 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 Overview Perform 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. • Lives in São Paulo/SP• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.• Written and verbal communication skills including good command of English language.• 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.

IQVIA Biotech is growing! Our team in Brazil has openings for Clinical Project Coordinators. This role can be home-based anywhere in Brazil. Job OverviewSupport, with minimal supervision, the Project Leader (PL) and Clinical Project Manager (CPM) with project management activities to ensure all work is conducted in accordance with standard operating procedures (SOPs), policies and practices, good clinical practices (GCP), applicable regulatory requirements, and meets quality/timeline metrics. Ensure customer satisfaction is met in relation to assigned project/s. Essential Functions• Assist in the establishment and maintenance of all project documentation including all files, records and reports according to the scope of work and standard operating procedures (SOPs).• Assist with periodic review/audit of files for accuracy and completeness.• Assist with the coordination and tracking of all information, communications, documents, materials, and supplies for assigned projects.• Manage study specific eTraining and oversee compliance.• Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information.• Prepare and distribute status, tracking and project finance reports, and assist the project manager(s) with budget allocation and approval of invoices.• Organize and support project leader (PL) in managing internal study team and customer meetings.• Take and record minutes, notes and actions at assigned meetings, distribute and follow up accordingly.• Support the preparation of presentation materials for meetings (internal/external) and project summary data.• Support the coordination of project team and/or customer meetings including logistics and materials required.• Identify and escalate discrepancies in project tracking data, timesheet coding, expense data billing etc.• Establish and manage performance dashboards, analyze event triggers and alerts and determine appropriate follow up for PL or others to act upon.• Monitor metrics and make required updates in IQVIA systems to ensure accurate and timely reporting is available to senior management.• Assist in the establishment and maintenance of all project documentation including all files, records and reports according to the scope of work and SOPs.• Coordinate onboarding of new Key Members and system access.• Assist in the training and orienting of more junior project support staff. Qualifications• Bachelor's Degree Bachelor's Degree in life sciences or other related field required Req• Typically requires 2-3 or more years of experience.• Requires good  knowledge within a specific discipline typically gained through extensive work experience and/or education.• 4 – 5 years’ experience or equivalent combination of education, training, and experience.• Knowledge of clinical trials - basic knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.;• Communication - strong written and verbal communication skills including good command of English language. Good communication and interpersonal skills.• Problem solving - good problem solving skills.• Quality - results and detail-oriented approach to work delivery and output. Good planning, time management, and prioritization skills. Attention to detail and accuracy in work.• IT skills - good software and computer skills, including MS Office applications.• Collaboration - ability to establish and maintain effective working relationships with coworkers, managers, and clients.• Cross-collaboration - ability to work across geographies displaying high awareness and understanding of  cultural differences. 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.

Care Specialist – Puerto RicoThe Care Specialist will be responsible to assist in the development of patient product support programs that will focus on treatment on-boarding and product related education, including supporting adherence to the treatment plan as prescribed. All materials used for this program for any purpose will be approved through the divisional review and approval process (STAR). Job Responsibilities:Assistance in the development of STAR-reviewed education plans covering a variety of topics, including: on boarding, product administration, adherence and compliance education to improve the patient-doctor dialogue for patients prescribed PRODUCTProduct related training and patient disease education to patients prescribed PRODUCTProvide education to support improved health literacy and dialogue between patients prescribed PRODUCT and their respective health care providersNever provide medical advice, instead referring patients to contact their healthcare providerDo not interfere with treatment decisions made between the patient and healthcare providerEducation to support prescribed therapy – supplemental injection and administration training, disease state and product-related information,Educational programs for HCP and office staff introducing the Multi-therapeutic Care Specialist patient support programSupport physician peer-to-peer engagement opportunities about the Care Specialist program by providing input to AbbVie concerning program content and/or by appearing as a speaker using STAR-approved content to introduce physicians to the program and resources available to patientsManaging accounts and patients case-load in a large geographyManagement of assigned travel and commercial budgets within OPPF standardsFollow all AbbVie-provided guidelines and policies and proceduresParticipate in, complete and follow all assigned training, from AbbVie and Service ProviderAny additional duties as assigned by program management and approved through the STAR teamRequired Qualifications:BA/BS degree, preferably in behavioral/social sciences, public health, or business-related disciplinesMust be licensed nurse (either LPN or RN)A minimum of 3 years professional experience in social work, case management or disease management in a patient/ health related fieldWilling to travel extensively (75-90%)Very strong time management skillsStrong planning and prioritization skillsStrong and effective presentation skills; excellent communications skills – both written and verbalProven success working with or within Community Based Organizations or other patient health-related, community focused organizations providing services to targeted populationsAbility to work and drive for results in cross-functional teamsInitiative and vision: challenge existing assumptions and interpretationsDrive and enthusiasmExceptional interpersonal skillsAbility to build relationships with third parties using good negotiation skillsWell-developed networking and influencing abilities to leverage relationships within and outside of the company.Fully competent in MS Office (Word, Excel, PowerPoint)Received injection trainingDriving is required for this role. Candidates must possess a valid driver’s license and will be subject to a review of their driving record prior to hire.Must reside in country where the job is posted.Note: This role is not eligible for visa sponsorship. Candidates must have authorization to work in the US without the need for sponsorship. #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 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 is $75,000 - $80,000 annually. 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: Merzig, Dillingen, Saarlouis 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.

Clinical Operations Project Managers are an integral part of clinical trial delivery, working closely with clinical teams and sponsors to improve patients' lives by bringing new drugs to market faster. Within a sponsor-dedicated Functional Service Provider (FSP) model, the Clinical Operations Project Manager (COPM) is an essential member of the core project team, responsible for the operational delivery of clinical studies at regional level. The COPM ensures studies are conducted in accordance with contractual requirements, timelines, quality standards, and applicable regulations. This role combines hands-on clinical operations oversight with strong project coordination and stakeholder management, with a particular focus on site-facing activities, CRA functional leadership, and execution excellence. Main Responsibilities Study Oversight & Delivery• Accountable for the execution of clinical trials in Italy and Greece, ensuring delivery according to timelines, budget, and quality expectations• Monitor study progress against milestones and proactively manage risks, issues, and contingencies• Ensure compliance with ICH-GCP, SOPs, and applicable regulatory requirements CRA Functional Management & Site Engagement• Provide functional oversight and guidance to assigned CRAs, ensuring high-quality monitoring and performance• Supervise CRA training at study level (protocol, monitoring plan, study tools, etc.)• Accompany CRAs on key visits (e.g., SIVs, audits) as needed to support study conduct and site engagement Quality & Compliance• Review and approve monitoring visit reports and follow-up communications• Ensure protocol adherence and oversee protocol deviations, root cause analyses, and CAPA implementation• Support inspection readiness and oversee audit findings resolution• Perform or support Study Evaluation Visits (SEVs) when required Project Coordination & Stakeholder Management• Act as a key interface between sponsor and operational teams, ensuring alignment and transparent communication• Collaborate cross-functionally to support milestone achievement and resolution of study issues Planning & Performance Management• Develop and maintain study plans and timelines, ensuring on-time delivery • Organize regular study follow-up meetings with CRAs and stakeholders• Provide structured feedback on team performance and contribute to continuous improvement   Required Skills and Qualifications• Bachelor’s degree in Life Sciences or related field • Minimum 3+ years as Project Manager and 5+ years of clinical research experience • Very good knowledge of clinical trial conduct, ICH-GCP, and regulatory requirements • Experience in set-up and conduct of Early Phase – Phase I and Phase II Clinical Trials • Therapeutic area knowledge in Oncology would be an advantage• Proven experience in site management, CRA oversight, and cross-functional coordination• Strong communication and stakeholder management skills• Ability to manage multiple priorities in a matrix environment• Very good command in English language • Strong operational leadership and coordination capabilities• Excellent problem-solving and risk management skills• Strong attention to quality, compliance, and detail• High level of collaboration across teams, functions, and geographies • Willingness to work at Sponsor's office in Rome for at least 3 days per week 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 53 200,00 € - 79 800,00 €. 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.

Role and Responsibilities The Application Security / DevSecOps Specialist role presents a hands on opportunity to support and scale IQVIA’s global Application Security and DevSecOps capabilities. We are deepening our DevSecOps capabilities, maturing AI security governance, and embedding security earlier into the software development lifecycle across a complex global environment — including cloud-native platforms, containerized workloads, third-party SaaS, and AI-enabled systems.This role is for a technically strong, practitioner-level leader who can operate at the intersection of engineering and security architecture. You will not only assess and advise — you will build, automate, and drive adoption of secure-by-design practices across IQVIA’s global delivery teams.You will sit within the global Information Security organization, collaborating closely with Security Architecture, Cloud Security, Vulnerability Management, and DevOps platform teams, as well as directly with product engineering and delivery teams across business units and regions. Principal responsibilities will include: •    Drive adoption and ownership of CI/CD security controls across product engineering teams, including tooling configuration, findings triage, pipeline onboarding, and remediation follow-through.•    Provide follow-up support for CI/CD security requests, including assisting teams with pipeline security tooling, configuration issues, findings remediation, and onboarding to DevSecOps services.•    Support application security assessments and security design reviews, working with delivery and architecture teams to identify risks, define mitigations, and track remediation actions.•    Act as a security point of contact for development teams, providing consultancy and guidance on secure coding practices, SDLC requirements, and secure architecture patterns.•    Review and assess application architectures, including cloud-native, microservices, APIs, containerized workloads, and event-driven systems, with an architectural security mindset.•    Support cloud application deployments and architecture patterns across Microsoft Azure and Amazon AWS, focusing on secure configuration, identity, network controls, and workload security.•    Contribute to the implementation and operationalization of DevSecOps practices, including SAST, DAST, SCA, container scanning, secret detection, and infrastructure-as-code security.•    Develop and maintain Python scripts and automations to support security checks, data analysis, reporting, or CI/CD integrations where appropriate.•    Support and contribute to AI Security for Development, including guidance on securing AI/ML architectures, protecting training pipelines, managing model risks, securing LLM prompt workflows, and addressing data leakage, model abuse, and agentic system risks.•    Assist in defining and maintaining security standards, requirements, and guidance related to application security, DevSecOps, cloud development, and AI-enabled systems.•    Collaborate closely with Security Architecture, Cloud Security, Vulnerability Management, and DevOps platform teams to ensure alignment with IQVIA security frameworks and toolsets.•    Track, follow up, and support security findings remediation, ensuring issues identified through assessments or pipeline tools are addressed effectively by delivery teams.•    Help promote Security by Design and Shift-Left principles, supporting teams early in design and development phases rather than late-stage security enforcement.  Required Experience and Qualifications •    Minimum of 6-8 years of professional experience in Application Security, DevSecOps, Software Engineering, Cloud Engineering, or related technical security roles.•    Hands on experience with CI/CD pipelines and DevSecOps tooling, including integrating security controls into build and deployment workflows.•    Working knowledge of application security testing techniques such as SAST, DAST, SCA, container scanning, and infrastructure as code security.•    Experience with cloud environments (Microsoft Azure and/or Amazon AWS), including deploying and securing applications in IaaS and PaaS platforms.•    Experience with containerized and modern application architectures, including Kubernetes, microservices, APIs, and event driven systems.•    Practical scripting experience, preferably in Python, for automation, integrations, or security tooling support.•    Knowledge of secure software development practices, OWASP Top 10, common application attack patterns, and secure coding principles.•    Foundational to intermediate knowledge of AI and ML security considerations, including Agent development, model risk, data protection, pipeline security, and misuse/abuse scenarios.•    Bachelor's degree in Computer Science, Software Engineering, Information Security, or equivalent practical experience is preferred.•    Security or cloud certifications (such as CSSLP, GWAPT, AWS/Azure Security, CKAD/CKS, or equivalent) are preferred but not mandatory.•    Working knowledge of security frameworks and standards such as NIST, OWASP, ISO 27001, or similar is an advantage.•    Strong communication skills, with the ability to work directly with engineering teams and explain security concepts in a practical, delivery focused manner. 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. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

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: Pforzheim, Baden-Baden, Rastatt 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.

Sell & Deliver – Associate PrincipalJoin a Ground‑Breaking AI Initiative at IQVIA IQVIA is building a world‑class team to deliver large‑scale AI solutions using cutting‑edge machine learning architectures. Our mission is to integrate data across clinical, real‑world, and biomedical sources to uncover new insights into patient trajectories—and transform how we understand and anticipate health outcomes. About the RoleWe are seeking an Associate Director or Associate Principal‑level Consultant to support the sales process and lead the delivery of AI‑driven projects in the Life Sciences R&D domain, with a strong focus on Clinical Development Optimization. This high‑impact, client‑facing role involves translating ambitious AI visions into practical, high‑value solutions. You will work closely with data scientists, engineers, clinicians, and domain experts, partnering with Principals while owning day‑to‑day delivery and contributing to the growth of IQVIA’s AI consulting capabilities in Pharma R&D. Key ResponsibilitiesClient Engagement & Business DevelopmentSupport opportunity shaping, proposal development, client presentations, and solution design.Serve as a day‑to‑day trusted partner to stakeholders across Pharma and Life Sciences.Help identify and develop new opportunities across Clinical R&D, especially where simulation and optimization can deliver impact.Contribute to the selling and delivery of novel, first‑in‑class AI solutions—including offerings still in development requiring co‑creation with clients.Support creation of compelling narratives around IQVIA’s newest AI systems and capabilities.Project Leadership & DeliveryLead hands‑on delivery of AI/ML projects focused on clinical development simulation using RWD, clinical trial data, omics, and other structured/unstructured sources.Own daily project execution ensuring high‑quality output, on‑time delivery, and strong client engagement.Coordinate cross‑functional project teams including data scientists, engineers, clinicians, and consultants.Support the development and client‑facing application of IQVIA’s next‑generation foundation model initiatives.Help design and implement scalable, high‑performance AI solutions using state‑of‑the‑art analytical techniques and platforms.Collaborate with third‑party technology partners across the AI and cloud ecosystem.Capability & Practice ContributionContribute delivery insights to shape IQVIA’s AI Life Sciences consulting offerings and repeatable solutions.Support mentoring and development of junior consultants and technical team members.Participate in thought leadership activities: client workshops, internal capability building, external presentations/publications.Help foster an agile, collaborative, impact‑driven delivery culture.Ideal Candidate ProfileMust‑Haves5–8+ years in Consulting, AI, Data Science, or Digital Transformation.Strong experience delivering complex analytics or AI‑driven projects in client settings.Solid understanding of AI/ML techniques (supervised, unsupervised, generative AI, LLMs, agentic AI).Life Sciences expertise—ideally within Pharma R&D, Clinical Trials, or Clinical Operations.Experience engaging senior client stakeholders and supporting strategic discussions.Proven ability to lead cross‑functional teams in fast‑paced, ambiguous environments.Strong ownership mindset and bias toward action.Nice‑to‑HavesExperience at a top‑tier consulting firm.Exposure to regulatory/data governance frameworks (HIPAA, 21 CFR Part 11).Experience with RWE, trial optimization, or biomarker‑based use cases.Familiarity with cloud/AI platforms: AWS, Azure ML, Databricks, foundation‑model ecosystems (ChatGPT, Claude).Exposure to agentic AI tools and modern AI development workflows.What We’re Looking ForPolymath mindset: Ability to combine strategic thinking, technical fluency, and relationship‑building.Entrepreneurial drive: Motivation to help build new capabilities and practices.“Jugaad” spirit: Creative, resourceful problem‑solving under uncertainty.Impact ambition: Desire to meaningfully influence how medicines are discovered, developed, and delivered.What We OfferA senior role within a high‑growth AI initiative reshaping innovation in Life Sciences.Opportunities to work with next‑generation foundation‑model capabilities.Clear growth paths toward Principal / Partner roles.Autonomy, flexibility, and strong support from senior leadership.Competitive compensation and incentive structure.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.

Our MedTech Device Field Collection Associate experiences a unique opportunity for collecting reprocessed medical equipment in a hospital. You will be working with surgical, non-invasive and vascular equipment within areas of the hospital such as Operating Rooms and Sterile Processing Departments. This is a great opportunity for you to gain medical experience!  You will have a flexible schedule and an opportunity to grow and expand into new opportunities while earning supplemental income and learning about the medical device industry.   What you will be doing in the role: Visit assigned hospitals weekly to collect products to be reprocessed Package and ship product to client manufacturing plant Document and log daily collections totals Notify the local Sales team of shipping supply needs Appropriate PPE is provided to all employees prior to the start of assignments. Available to work approximately 12-15 hours a week Training for this role will be provided and is paid Job Requirements:   An active and unrestricted driver license is required for this position  Minimum High school diploma or equivalent Reliable vehicle for transportation Must be comfortable with basic software programs and Microsoft operating system  Excellent customer service skills and strong attention to detail Ability to lift 30-50 lbs Ability to clear hospital vendor credentialing requirements, including proof of vaccination status, required  Travel Requirement: Travel locally for up to 2-3 hours to support customer needs Must have an active driver license and a personal vehicle to use for job related assignments Travel time is paid, as is mileage Preferred Attributes: Experience in healthcare, general labor, warehouse or customer service, is beneficial for this position. Ability to work independently in customer settings with minimal supervision. IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities. Benefits: This position is not eligible for our Medical Benefits. Vaccine/Immunization/Hospital Credentialing Requirement: A required function of this job requires individuals to enter various healthcare facilities.  Thus, upon selection, individuals must complete healthcare facility credentialing process.  To obtain credentials, individuals must meet the immunization requirements specified by the facility.  Individuals are typically required to have completed/up to date: Measles, Mumps & Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria & Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series (heavily enforced by most facilities, some require booster(s)). Please note, IQVIA complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons, however, our client’s requirements may supersede this.  *Please note: No relocation is being offered for this role. Candidate must live locally to be considered. Due to the nature of this role, it is not eligible for Visa sponsorship. LFT1 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 $51,400.00 - $128,400.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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: Mönchengladbach   Das sind Deine Aufgaben: Durch die direkte Ansprache und intensive Betreuung ausgewählter Allgemeinmediziner, Internisten und Praktiker förderst Du die Verordnung Deines Impfstoff-Präparats und trägst so maßgeblich zum Unternehmenserfolg bei. In sehr eigenständiger Arbeitsweise bist du für den Aufbau und die Pflege langfristiger Beziehungen zu Ärzten und dem medizinischen Fachpersonal verantwortlich. Als Experte setzt Du auf der Basis Deines Fachwissens Beratungsstrategien erfolgreich um und überzeugst so Deine Ansprechpartner. Die Überwachung und das Management des Impfstoffbestands Deiner Kunden hast Du immer im Blick und stellst so eine kontinuierliche Verfügbarkeit und Versorgung sicher. Du erstellst eine eigenständige Routenplanung und pflegst Deine Besuche im CRM-System, inkl. Vor- und Nachbereitung. Das bringst Du mit: Du verfügst über eine naturwissenschaftliche Ausbildung (idealerweise Hochschulabschluss) oder Ausbildung zum Geprüften Pharmareferent (m/w/d) gemäß §75 AMG. Idealerweise verfügst Du über Erfahrung im Vertrieb von Impfstoffen bzw. hast eine hohe Bereitschaft und Begeisterung, Dich als Neueinsteiger in ein neues Aufgabengebiet einzuarbeiten. 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, runden Dein Profil ab. 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) 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 #Impfstoff #Chemie #Pharmareferent #75AMG #IQVIA #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.

We are seeking Senior Lab Project Services Coordinator to join IQVIA Laboratories at Mississauga, ON.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:Provide day-to-day project support across the study lifecycle by coordinating routine procedures, documentation, monitoring activities and stakeholder communications. This role helps ensure study deliverables are completed in line with standard operating procedures, protocol requirements, policies and good practices. What You'll Be Doing:Support study setup and planning by attending meetings, preparing minutes and action logs, and creating protocol-specific laboratory instruction documentsCoordinate routine study activities including site loading, Investigator Portal access, kit shipments, centralized monitoring support and close-out tasksMonitor day-to-day study performance, identify trends using status reports and monitoring tools, and communicate findings to internal and external teamsAssist with administrative study tasks, monitoring plans, reports, protocol-specific materials and document quality control reviewsManage query follow-up, protocol questions, issues and escalations with internal and external stakeholders to support timely resolutionLead customer communications and meeting activities when the Project Manager is absent and support project launch and close-out activitiesContribute to study training, audits, inspections, process improvement initiatives and mentoring of more junior staff What We Are Looking For:High School Diploma or equivalent required; Bachelor’s Degree in Life Sciences or a related field preferred1-3 years relevant experience (in the Clinical, Medical or Healthcare industry preferred)Computer proficiency in word processing, presentation and spreadsheet applicationsExperience using status reports, monitoring tools and outputs to proactively identify trends and support study performanceOther Equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Strong interpersonal, written and verbal communication, organizational and time management skillsDemonstrated ability to handle multiple competing priorities, think critically and solve problems effectively in a fast-paced environmentAbility to establish and maintain effective working relationships with coworkers, managers, customers and investigator sitesAbility to utilize resources effectively and maintain high-quality outputs aligned to protocol and customer expectations 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 est un fournisseur mondial de premier plan de services de recherche clinique, d'informations commerciales et de renseignements sur les soins de santé pour les secteurs des sciences de la vie et de la santé.  IQVIA se consacre à accélérer le développement et la commercialisation de traitements médicaux innovants pour aider à améliorer les résultats des patients et la santé de la population dans le monde entier. Pour en savoir plus, visitez https://jobs.iqvia.com   IQVIA est fière d’être un employeur souscrivant au principe de l’égalité d’accès à l’emploi. Tous les candidats qualifiés seront pris en considération pour un emploi sans égard à la race, la couleur, la religion, le sexe, l’orientation sexuelle, l’identité de genre, l’origine nationale, le handicap, l’âge, l’état matrimonial ou tout autre statut protégé par la loi applicable.  Des mesures d’adaptation pour les candidats handicapés sont disponibles sur demande dans tous les aspects du processus de recrutement. Si vous avez un handicap qui nécessite une mesure d’adaptation, nous vous encourageons à contacter notre équipe d’acquisition de talents au [email protected], afin qu’IQVIA puisse soutenir votre participation au processus de recrutement. IQVIA s’engage à faire preuve d’intégrité dans son processus de recrutement et applique une politique de tolérance zéro en matière de fraude des candidats. Toutes les informations et toutes les qualifications soumises dans votre candidature doivent être véridiques et complètes. Toute fausse déclaration, présentation trompeuse ou omission importante au cours du processus de recrutement entraînera la disqualification immédiate de votre candidature, ou la cessation d’emploi si elle est découverte ultérieurement, conformément aux lois applicables. Nous apprécions votre honnêteté et votre professionnalisme. Veuillez noter qu'il est possible que nous utilisions l'intelligence artificielle (IA) dans le traitement de votre candidature. Cependant, nous utilisons l'IA uniquement pour aider notre équipe de recrutement à sélectionner ou à évaluer les candidatures, et non pas pour remplacer la prise des décisions par les membres de notre équipe. 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, age, marital status, or any other status protected by applicable law.  Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. If you have a disability that requires an accommodation, we encourage you to contact our Talent Acquisition Team at: [email protected], so that IQVIA can support your participation in the recruitment process. 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. Please note that we may use artificial intelligence (AI) in the processing of your application. However, we only use AI to assist our recruitment team with the screening or assessment of candidacies, and not as a substitute for human decision-making. La fourchette salariale de base potentielle pour ce poste, annualisée, est de $60,000.00 - $100,000.00. Le salaire de base réel offert peut varier selon plusieurs facteurs, notamment les qualifications liées à l’emploi telles que les connaissances, les compétences, la formation et l’expérience; l’emplacement; et/ou l’horaire (temps plein ou temps partiel). Selon le poste offert, des régimes d’incitation, des primes et/ou d’autres formes de rémunération peuvent être proposés, en plus d’une gamme d’avantages sociaux liés à la santé, au bien-être et/ou d’autres bénéfices.  The potential base pay range for this role, when annualized, is $60,000.00 - $100,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and wellness 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. Enfermera para Programa de Soporte a Pacientes Requisitos Grado académico: Técnico o Lic. en enfermería (cédula profesional). Experiencia necesaria en instituciones de Gobierno: IMSS y/o INSABI. Se toman en cuenta Prácticas profesionales y/o Servicio Social.Manejo de procesos administrativos. Esta posición es 100% administrativa, no clínica, considera este aspecto.Disponibilidad para trabajar visitando hospitales de gobierno y/o privados: 80% campo / 20% administrativo.ALTA DISPONIBILIDAD PARA VIAJAR. Es una actividad fíja y constante de la posición. La persona se encargara de su Estado Base y de los Estados de la República Asignados. Las zonas a visitar se establecen con base en las necesidades del programa.Disponibilidad de horio.Gusto por la atención al paciente y/o cuidador primario y brindarle soporte en dudas e inquietudes.Seguimiento a procesos administrativos y farmacovigilancia.Competencias OrganizaciónComuniación efectivaTrabajo en equipoTrabajo bajo presiónAtención a pacientesActividades: Acudir a diferentes instituciones de salud para poyar en todos los trámites administrativos para que los pacientes puedan calificar y que se apruebe su tratamiento de alto costo en hospitales de gobierno y/o privados.Visitar a médicos tratantes.Invitar a pacientes en tratamiento para participar en el programa de soporte a pacientes y hablarles de los beneficios de pertenecer en el programa.Monitorear el estado del tratamiento en CRM de los pacientes.Dar seguimiento a pacientes vía telefónica, con la finalidad de saber su estado actual de tratamiento y en caso de que alguno muestre alguna reacción adversa al tratamiento, se reporta a farmacovigilancia.Verificar que los pacientes reciban a tiempo sus tratamientos de acuerdo con las indicaciones del médico.Reportar actividades realizadas al Supervisor y Call Center.Capturar información de pacientes diariamente en sistema CRM (nuevos y actuales).Realizar solicitud de materiales a Call Center para médicos y pacientes.Programar viajes fuera de su localidad.Presentar plan de trabajo quincenal o mensual.Enviar reporte de comprobación de gastos.Importante: Trabajo de lunes a viernesTrabajo de tiempo completoNo se rolan turnosZona de trabajo: Guadalajara y Estados de la República asignadosInteresadas (os) favor de aplicar por este medio. Tipo de puesto: Tiempo completo #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.

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. We are looking for a skilled Data Engineer to join a 6-month project based in Mexico City. The ideal candidate will have strong experience in modern data engineering practices, particularly in Databricks, Apache Spark, and AWS environments. You will play a key role in designing, building, and optimizing scalable data pipelines and data architectures. Key ResponsibilitiesDesign, develop, and optimize data pipelines using Databricks and Apache SparkImplement and maintain ETL/ELT workflowsDevelop data models to support analytics and reporting needsWork with Delta Lake for reliable and consistent data storageCollaborate with cross-functional teams to deliver high-quality data solutionsEnsure best practices in version control, CI/CD, and code qualitySupport data architecture following Medallion (Bronze, Silver, Gold) principlesRequired Qualifications3+ years of experience working as a Data EngineerStrong hands-on experience with DatabricksExpertise in Apache SparkAdvanced knowledge of SQL and data modelingExperience working with Delta LakeProficiency in PythonHands-on experience with AWS cloud platformsAdvanced EnglishTools & TechnologiesETL orchestration tools (e.g., Apache Airflow)Version control systems (e.g., Git)CI/CD pipelinesFamiliarity with Medallion ArchitectureNice to HaveExperience working with EHS (Environmental, Health & Safety) or ESG (Environmental, Social, and Governance) data and processes#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.

IQVIA Biotech is growing! Our team in Mexico has openings for Clinical Project Coordinators. This role can be home-based anywhere in Mexico. Job OverviewSupport, with minimal supervision, the Project Leader (PL) and Clinical Project Manager (CPM) with project management activities to ensure all work is conducted in accordance with standard operating procedures (SOPs), policies and practices, good clinical practices (GCP), applicable regulatory requirements, and meets quality/timeline metrics. Ensure customer satisfaction is met in relation to assigned project/s. Essential Functions• Assist in the establishment and maintenance of all project documentation including all files, records and reports according to the scope of work and standard operating procedures (SOPs).• Assist with periodic review/audit of files for accuracy and completeness.• Assist with the coordination and tracking of all information, communications, documents, materials, and supplies for assigned projects.• Manage study specific eTraining and oversee compliance.• Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information.• Prepare and distribute status, tracking and project finance reports, and assist the project manager(s) with budget allocation and approval of invoices.• Organize and support project leader (PL) in managing internal study team and customer meetings.• Take and record minutes, notes and actions at assigned meetings, distribute and follow up accordingly.• Support the preparation of presentation materials for meetings (internal/external) and project summary data.• Support the coordination of project team and/or customer meetings including logistics and materials required.• Identify and escalate discrepancies in project tracking data, timesheet coding, expense data billing etc.• Establish and manage performance dashboards, analyze event triggers and alerts and determine appropriate follow up for PL or others to act upon.• Monitor metrics and make required updates in IQVIA systems to ensure accurate and timely reporting is available to senior management.• Assist in the establishment and maintenance of all project documentation including all files, records and reports according to the scope of work and SOPs.• Coordinate onboarding of new Key Members and system access.• Assist in the training and orienting of more junior project support staff. Qualifications• Bachelor's Degree Bachelor's Degree in life sciences or other related field required Req• Typically requires 2-3 or more years of experience.• Requires good  knowledge within a specific discipline typically gained through extensive work experience and/or education.• 4 – 5 years’ experience or equivalent combination of education, training, and experience.• Knowledge of clinical trials - basic knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.;• Communication - strong written and verbal communication skills including good command of English language. Good communication and interpersonal skills.• Problem solving - good problem solving skills.• Quality - results and detail-oriented approach to work delivery and output. Good planning, time management, and prioritization skills. Attention to detail and accuracy in work.• IT skills - good software and computer skills, including MS Office applications.• Collaboration - ability to establish and maintain effective working relationships with coworkers, managers, and clients.• Cross-collaboration - ability to work across geographies displaying high awareness and understanding of  cultural differences. 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.

We are seeking Laboratory Project Services Coordinator to join IQVIA Laboratories at Marietta, GA.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 Project Manager and project team by coordinating routine laboratory project activities across the full study lifecycle, from study start-up through close-out. Help ensure study deliverables are completed accurately, on time, and in line with standard operating procedures, protocol requirements, and customer expectations. What You'll Be Doing:Support study setup activities by attending meetings, preparing minutes and action logs, and assisting with protocol-specific laboratory instruction documentsCoordinate day-to-day study activities including site loading, Investigator Portal access, kit shipments, and centralized monitoring supportMonitor study performance using status reports and tracking tools, and identify trends that may require escalation or follow-upPartner with internal and external stakeholders to resolve queries, protocol questions, issues, and escalations in a timely mannerCommunicate with customers and study teams, including leading key communications and activities when the Project Manager is absentSupport study close-out activities and help ensure project outputs meet protocol, organizational, and customer requirementsParticipate in meetings, audits, inspections, and study training activities with sites, CRAs, and customers as needed What We Are Looking For:High School Diploma or equivalent required; Bachelor's Degree in Life Sciences or related field preferred1+ years relevant experience (Clinical, Medical or Healthcare industry preferred)Computer proficiency in word processing, presentation and spreadsheet applicationsAbility to use status reports, monitoring tools, Investigator Portal workflows, and site activity tracking to support study oversightOther Equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Strong interpersonal, written, and verbal communication skills with a good command of English languageDemonstrated ability to manage multiple competing priorities, think critically, and solve problems effectivelyStrong organizational and time management skills in a fast-paced environmentAbility to establish and maintain effective working relationships with coworkers, managers, customers, and external partnersAbility to lift up to 50 lbs, frequent standing and walking, occasional sitting, close eye work requirement (computer, typing, reading small prints). Physical demands vary depending on assigned work area and work tasks. Occasional exposure to cold temperatures. 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 $43,000.00 - $89,500.00. 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 unseren Kunden, ein renommiertes, international agierendes Familienunternehmen, suchen wir zum nächstmöglichen Zeitpunkt einen Pharmaberater (m/w/d) General Medicine / Diabetes Im Gebiet: Idar-Oberstein, Sankt Wendel, Illingen 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.

Join us on our exciting journey!We are recruiting a new Technical Support Analyst (Tier 1) with work experience in the area and native in Polish language. Under general supervision, provide high quality phone-based service desk support to end users regarding IT problems and service requests. If you want to play a key role in a multicultural, dynamic and committed team this could be the role for you! Essential Functions: • Use remote control tools like gotoassist to solve a large percentage of incident calls on the first interaction with the customer.• Analyze data points from monitoring tools and reporting systems to determine the root cause of a problem and perform the necessary functions to resolve the problem.• Adhere to established IT policies, procedures and standards and ensure conformance with information systems goals and procedures.• Provide management with information on problems that are severe in nature or that are exceeding target dates.• Maintain a thorough working knowledge of the day-to-day operating environment, available tools, and client applications. Maintain a working knowledge of Service Desk and IT Operations procedures related to client services.• Provide assistance in the areas of site support, and project specific assignments. Provide training as needed to end-users.• Provide support for business applications.• Perform other duties as required. Qualifications: • High School Diploma or equivalent and 3 years IT experience; or equivalent combination of education, training and experience.• Working knowledge of Microsoft server, workstation and networking technologies.• Working knowledge of industry standards with regards to system and network administration.• Possess excellent verbal and written communication skills.• Ability to solve PC related problems utilizing remote control tools.• Strong analytical and troubleshooting skills. Soft Skills:  Problem-Solving & Critical ThinkingAnalytical ThinkingCommunication Skills (Clear & Professional)Attention to DetailAccountability & ResponsibilityAdaptability & Learning AgilityTime Management & Prioritization EmpathyCustomer Focus Collaboration & TeamworkWe invite you to join IQVIA™ IQVIA™ is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com IQVIA™ is an equal opportunity employer. We make employment decisions based on qualifications and merit. We prohibit discrimination based on any unlawful consideration such as age, race, national origin, gender or other "protected status“. 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. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

🎯 Descripción del puesto: Buscamos un/a Delegado/a Comercial Senior, con clara orientación a ventas y amplia experiencia en el canal farmacia, para la apertura de nuevas farmacias y la gestión comercial de una cartera existente. El puesto tiene un perfil 100% comercial, siendo el objetivo principal el crecimiento en ventas y captación de clientes. Otras funciones como formación o acciones de visibilidad en punto de venta (sell out) serán secundarias frente a la actividad comercial. 🧩 Funciones principales: - Captación y apertura de nuevas farmacias. - Gestión y desarrollo comercial de farmacias activas (venta presencial). - Incremento de ventas y fidelización de clientes. - Ejecución de acciones comerciales en el punto de venta. - Realización puntual de formaciones y acciones de visibilidad cuando sea necesario. ✅ Requisitos imprescindibles: - Perfil Senior, con experiencia demostrable en ventas. - Experiencia previa en venta a farmacias y/o distribución farmacéutica. - Clara orientación a resultados y fuerte capacidad de negociación. - Autonomía, proactividad y mentalidad comercial. - Experiencia en gestión de cartera y apertura de clientes ✨ ¿Qué ofrecemos? 💼 Proyecto estable y en expansión 📚 Formación continua y desarrollo profesional 🤝 Entorno dinámico y colaborativo donde tu talento marcará la diferencia Si buscas un reto profesional que combine especialización, autonomía y proyección, ¡Envíanos tu candidatura y únete a nuestro equipo! 💪 #LI-CES #LI-DNP 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. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

We are seeking a dedicated Epidemiology professional to support the design and delivery of high-quality real-world evidence studies in a global, cross-functional environment. The role would entail to partner with global clients and cross-functional teams to lead epidemiology for real-world studies across the full product lifecycle, from early clinical development through post-approval. Responsibilities range from feasibility assessments to developing protocols and clinical study reports, with opportunities to support business development and strengthen client relationships. Essential Functions: Lead the design and implementation of epidemiology and pharmacoepidemiology methods in real-world studies, including drug safety, effectiveness, and observational research. Translate research objectives into fit-for-purpose study designs (e.g., cohort, case-control, cross-sectional, pragmatic, survey-based), defining endpoints, populations, and analytic strategies. Serve as project lead on smaller studies or support larger client-facing and internal projects. Author protocols, reports, and study documents, ensuring quality, completeness, and timely delivery. Provide epidemiological input into statistical analysis plans and review analysis outputs. Contribute to CRF/eCRF design, form reviews, and other project deliverables (e.g., regulatory responses, presentations). Support client interactions and communications, with senior oversight as needed. Identify and escalate project, budget, or client-related risks and issues. Ensure work is delivered within agreed budgets and timelines. Contribute to process improvements and the development of best practices. Support business development activities, including proposal content for smaller projects. Represent the organization externally (e.g., conferences, presentations) as appropriate. Oversee or conduct statistical analyses when required. Contribute to proposal development and internal initiatives in epidemiology and observational research. Qualifications: Master's Degree Graduate education in epidemiology, pharmacoepidemiology, public health with concentration in epidemiology, pharmacy with concentration in epidemiology or relevant scientific field and 5 years relevant experience Req or Ph.D. with 2 years relevant experience is preferred. Sound methodological training in epidemiology, pharmacoepidemiology, public health with concentration in epidemiology, pharmacy with concentration in epidemiology or related area relevant to observational health research. Ability to design, plan and conduct observational studies of comparative effectiveness and safety. Excellent oral and written communication skills in English, medical writing experience beneficial. Ability to establish and maintain effective working relationships with coworkers, managers and clients in a global and matrixed environment. Exceptional attention to detail and the ability to effectively prioritize and manage multiple tasks. Ability to work collaboratively with diverse team members. Must be proficient in Word, Excel, PowerPoint and Edge. Ability to read outputs from SAS, R or other programming languages. Must be highly organized and self-motivated with ability to determine and meet objectives. 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. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

The Customer Success Lead is accountable for establishing and scaling a consistent Customer Success capability across the HSS Business Unit, ensuring post‑go‑live value realisation, adoption, and renewal risk management across RBUs.This role partners with Delivery Leads, Support, GTM Practices, and Product to create a closed‑loop operating model from implementation to outcomes, using structured health metrics and proactive engagement to improve client experience, reduce escalations, and protect renewal and expansion potential. Key Responsibilities Customer Success Operating Model•    Define the global Customer Success model for HSS (roles, playbooks, engagement cadence, health scoring, QBR approach).•    Clarify handoffs from Delivery to Customer Success and from Support into Customer Success for proactive risk management.•    Set standards for post‑go‑live value tracking, adoption programs, and renewal governance. Client Outcomes & Retention•    Own customer health frameworks and leading indicators of risk (usage/adoption, open issues, value milestones, stakeholder engagement).•    Drive structured renewal readiness and executive sponsor engagement in partnership with RBUs and Practices.•    Coordinate remediation plans for at‑risk accounts with Delivery and Support leaders. Feedback Loops into Product & Delivery•    Create structured feedback loops into Product and Delivery (feature gaps, workflow pain points, recurring adoption barriers).•    Partner with Support to ensure knowledge and problem management insights inform Customer Success actions.•    Ensure GTM and Practices have visibility into client outcomes to improve pipeline quality and expansion strategy. Capability Building & Enablement•    Build and develop Customer Success leaders across RBUs; define training and enablement.•    Standardise customer communication templates, success plans, and governance formats.•    Drive a customer-centric culture focused on measurable outcomes and proactive management.Experience & Qualifications•    Bachelor’s degree required; advanced degree preferred.•    8+ years in Customer Success, account management, service delivery, or consulting roles with strong client-facing leadership.•    Proven experience establishing customer success frameworks (health scoring, value realisation, renewal governance).•    Strong stakeholder management and ability to operate across Delivery, Support, GTM, and Product organisations.•    Data-driven approach to measuring outcomes and operationalising customer feedback. Preferred Experience•    Experience in healthcare/provider technology solutions or life sciences services.•    Experience managing enterprise, multi-country client relationships.•    Familiarity with delivery-to-operations transitions and support escalation dynamics. What Success Looks Like in This Role•    Improved adoption and value realisation post‑go‑live; reduced renewal and escalation risk.•    Earlier identification and mitigation of at‑risk accounts through structured health management.•    Stronger closed‑loop feedback into Product and Delivery; fewer recurring issues and smoother expansions.•    More consistent customer experience across RBUs with clearer ownership of outcomes. 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. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.