IQVIA

Ausbildung Fachinformatik Anwendungsentwicklung (w/m/d) Der Gesundheitsmarkt steht vor einem digitalen Wandel (e-Rezept, e-Akte). Seit über 30 Jahren agieren wir bereits als führender Anbieter von Softwarelösungen und Dienstleistungen für den Gesundheitsmarkt – dabei sind individuelle Softwareprodukte sowie innovative Anwendungen und Dienstleistungen unser Kerngeschäft. Durch die Mitarbeit in engagierten und motivierten Teams lernst Du unsere abwechslungsreichen und anspruchsvollen Aufgabengebiete kennen. Du bist ein Teamplayer, denkst gern analytisch und scheust dich nicht vor Herausforderungen? Dann bewirb dich bei uns! Wir freuen uns schon jetzt auf dich. Aufgaben Als Fachinformatiker(in) Anwendungsentwicklung lernst du, Softwareanwendungen zu konzipieren, zu entwickeln, zu testen und zu dokumentieren. Natürlich gehört auch das Beheben von Fehlern dazu. Außerdem vertiefst du bei uns die Entwicklung und Optimierung von Datenbanken sowie die Erstellung von SQL-Abfragen zur Verarbeitung und Auswertung von Daten. Wir unterstützen Dich mit Rat & Tat bei der Vorbereitung auf Deine anstehende Prüfung und Facharbeit. Voraussetzungen Du hast das Abitur erfolgreich abgeschlossen oder einen guten Realschulabschluss. Deine Allgemeinbildung ist gut, genauso wie deine Englischkenntnisse und du hast gute Noten in Mathematik und Informatik. Du hast Lust, im Team zu arbeiten sowie die Fähigkeit, Aufgaben auch selbstständig zu lösen. Du besitzt ein hohes Maß an Eigeninitiative sowie die Motivation, dich gern neuen Herausforderungen zu stellen. Du hast Spaß bei der Arbeit am Computer. Du bringst ein technisches Grundverständnis und logisches Denkvermögen mit. Deutschkenntnisse auf Niveau C1 und gute Englischkenntnisse in Wort und Schrift runden dein Profil ab. Das erwartet Dich außerdem: Mentoren-Programm und strukturierte Begleitung während der kompletten Ausbildung Kolleg:innen mit fachlicher Expertise, die dich mit Rat & Tat unterstützen, auch in Vorbereitung auf die anstehende Prüfung und deine Facharbeit Tolle Karriere- und Entwicklungsmöglichkeiten Persönliche und fachliche Weiterbildung  Übernahme der Kosten für Lernmaterialien und Gebühren im Rahmen der Ausbildung Subventioniertes Essen sowie kostenlose Kalt- und Heißgetränke Gute Chancen zur Übernahme nach erfolgreich abgeschlossener Ausbildung Ausbildungsvergütung von 840,00 € brutto im 1. LJ, 890,00 € brutto im 2. LJ und 940,00 € brutto im 3. LJ Wir freuen uns auf Deine Bewerbung mit Anschreiben, Lebenslauf und Abschlusszeugnis/ den letzten beiden Endjahreszeugnissen. Wir schätzen Vielfalt und begrüßen daher alle Bewerbungen – unabhängig von Geschlecht, Nationalität, ethnischer und sozialer Herkunft, Religion/Weltanschauung, Behinderung, Alter sowie sexueller Identität. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. Collaborate with clinical team on 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 and completeness. Collaborate with CRAs and RSU on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. Coordinate 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. Act as a mentor for less experienced Clinical Trial Assistants (CTAs). Assist with training and onboarding of new CTAs. May serve as subject matter expert for business processes. May lead CTA study teams. May assist with interviewing and screening of potential new team members May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training. May participate in departmental quality or process improvement initiatives. Qualifications High School Diploma or equivalent 5 administrative support experience. Equivalent combination of education, training and experience. Minimum two years clinical research experience strongly preferred. Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint. Effective written and verbal communication skills including good command of English language. Effective time management and organizational skills. Ability to establish and maintain effective working relationships with coworkers, managers, and clients. Knowledge 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™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 88.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebs teams 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 suchen wir Pharmaberater (m/w/d) zum nächstmöglichen Zeitpunkt für den Arzt-Außendienst Im Gebiet: Falkensee, Oberhavel, Templin Das sind Deine Aufgaben: Du besuchst nach einer umfangreichen Produktschulung regelmäßig die niedergelassenen Ärzte Ihres Indikationsgebietes (u. a. Atemwegserkrankungen), um diese über die Kundenprodukte zu informieren und zu beraten. Zu deinen Aufgabenfeldern gehört neben der Organisation ärztlicher Fortbildungs-veranstaltungen auch die Teilnahme an Ärztekongressen und Zyklustagungen. Wiederkehrende Weiterbildungen in deiner Region sowie der aktive Austausch im Team bietet dir die Chance auf eine erfolgsorientierte Entwicklung im Außendienst. Neben der Besprechung von innovativen Produkten hast du als Pharmareferent die Möglichkeit, neuartige Plattformen der Kommunikation zwischen Arzt und Patient zu etablieren. Das bringst Du mit: Du verfügst über eine Naturwissenschaftliche Ausbildung (idealerweise Hochschulabschluss) oder Ausbildung zum Geprüften Pharmareferent (m/w/d) gemäß §75 AMG. Als durchsetzungsstarke Persönlichkeit und erfahrener Netzwerker verstehst du es, deine Ansprechpartner zu begeistern. Du möchtest etwas bewegen – für dein Präparat, für dich selbst und vor allem für betroffene Patienten. Du hast Ausgeprägte kommunikative Fähigkeiten, soziale Kompetenz und bringst die Bereitschaft mit, eigenverantwortlich und ergebnisorientiert zu arbeiten. Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] #LI-CES #LI-DNP #LI-SS2 #Pharmaberater #Biologie #Chemie #Pharmareferent #BTA #CTA #PTA #Oecotrophologie #Pharmazie #Pharma-Außendienst #b-c-a-g 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.

To be eligible for this position, you must reside in the same country where the job is located. Job OverviewEstablish and manage an effective business development program to maximize organization growth.  Serve as overall customer relationship manager and strategic business partner responsible for developing and expanding new business opportunities with customers. Essential Functions Maintain in-depth knowledge of all IQVIA services for appropriate cross-sell opportunities. Actively prospect and leverage potential new business opportunities within specified potential new and/or existing Customers/Accounts. Establish and execute a comprehensive sales plan for each target account. Cultivate strong, long-term relationships with key decision-makers within Account and develop deep knowledge of the customer organization. Actively network in the industry to establish relationships and to identify potential opportunities. Aggressively pursue awareness of competitive activities, positioning and pricing, which includes specific reasons for awards and non-awards. Continuously monitor status of leads and opportunities to ensure a pipeline of opportunities is maintained. Analyze potential opportunities and develop sales strategies for each customer account. Ensure appropriate strategy/solution is proposed to customer.   Monitor actions and results against plans. Establish brand recognition; communicate with internal Project Managers to assess overall level of customer satisfaction and progress of projects. Work with operations and functional managers to identify sales team and prepares and leads the sales presentation. Educate team participants in customer culture, operational needs/methods and sales techniques needed to close the sale. Coordinate with contracts and proposals to develop proposal. Handle follow-up related to the sale and drive completion of contractual documents. Utilize CRM to establish reports and dashboards to analyze business development and sales activities and track progress. Maintain high visibility within customer organization. Plan and coordinate all customer sales activities. Communicate all account activity to Senior Sales Leader and/or appropriate individuals through the CRM system. Lead/participate in change management initiatives for the sales organization. Provide overall support and serves as a mentor for junior sales staff members. Qualifications Bachelor's degree in business management Req 15 years relevant industry experience (CRO/Pharmaceutical) Req Or Equivalent combination of education, training, and experience Req Proven track record at developing mid-level and high-level contacts Solid understanding of commercialization and the principles of drug discovery and development Excellent skills using Microsoft Office Suite: MS PowerPoint, MS Word, and MS Excel Excellent oral and written communication skills Strategic business awareness and analytical skills Adaptability and flexibility to changing priorities Demonstrated ability to work creatively and effectively in a fast-paced environment Attention to detail and ability to work simultaneously on multiple priorities Ability to maintain demanding timelines Ability to influence others both internally and externally Ability to work independently and as a team player Ability to establish and maintain effective working relationships with coworkers, managers and clients 30% travel is required (based on location). 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 $125,300.00 - $349,000.00. 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 welfare and/or other benefits.

Ausbildung Fachinformatik Anwendungsentwicklung (w/m/d) A Der Gesundheitsmarkt steht vor einem digitalen Wandel (e-Rezept, e-Akte). Seit über 30 Jahren agieren wir bereits als führender Anbieter von Softwarelösungen und Dienstleistungen für den Gesundheitsmarkt – dabei sind individuelle Softwareprodukte sowie innovative Anwendungen und Dienstleistungen unser Kerngeschäft. Durch die Mitarbeit in engagierten und motivierten Teams lernst Du unsere abwechslungsreichen und anspruchsvollen Aufgabengebiete kennen. Du bist ein Teamplayer, denkst gern analytisch und scheust dich nicht vor Herausforderungen? Dann bewirb dich bei uns! Wir freuen uns schon jetzt auf dich. Aufgaben Als Fachinformatiker(in) Anwendungsentwicklung lernst du, Softwareanwendungen zu konzipieren, zu entwickeln, zu testen und zu dokumentieren. Natürlich gehört auch das Beheben von Fehlern dazu. Dabei verwendest du Entwicklungswerkzeuge wie Java, Spring und Maven. Wir unterstützen Dich mit Rat & Tat bei der Vorbereitung auf Deine anstehende Prüfung und Facharbeit. Voraussetzungen Du hast das Abitur erfolgreich abgeschlossen oder einen guten Realschulabschluss. Deine Allgemeinbildung ist gut, genauso wie deine Englischkenntnisse und du hast gute Noten in Mathematik und Informatik. Du hast Lust, im Team zu arbeiten sowie die Fähigkeit, Aufgaben auch selbstständig zu lösen. Du besitzt ein hohes Maß an Eigeninitiative sowie die Motivation, dich gern neuen Herausforderungen zu stellen. Du hast Spaß bei der Arbeit am Computer. Du bringst ein technisches Grundverständnis und logisches Denkvermögen mit. Deutschkenntnisse auf Niveau C1 und gute Englischkenntnisse in Wort und Schrift runden dein Profil ab. Das erwartet Dich außerdem: Mentoren-Programm und strukturierte Begleitung während der kompletten Ausbildung Kolleg:innen mit fachlicher Expertise, die dich mit Rat & Tat unterstützen, auch in Vorbereitung auf die anstehende Prüfung und deine Facharbeit Tolle Karriere- und Entwicklungsmöglichkeiten Persönliche und fachliche Weiterbildung  Übernahme der Kosten für Lernmaterialien und Gebühren im Rahmen der Ausbildung Gute Chancen zur Übernahme nach erfolgreich abgeschlossener Ausbildung Ausbildungsvergütung von 840,00 € brutto im 1. LJ, 890,00 € brutto im 2. LJ und 940,00 € brutto im 3. LJ Wir freuen uns auf Deine Bewerbung mit Anschreiben, Lebenslauf und Abschlusszeugnis/ den letzten beiden Endjahreszeugnissen. Wir schätzen Vielfalt und begrüßen daher alle Bewerbungen – unabhängig von Geschlecht, Nationalität, ethnischer und sozialer Herkunft, Religion/Weltanschauung, Behinderung, Alter sowie sexueller Identität. 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.

Project Management Analysts (PMA) are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The PMA works in partnership with the Project Leader (PL)/Clinical Project Manager (CPM) providing support with project management activities to mitigate risk, control cost, manage project schedule, and ensure customer satisfaction related to assigned project/s. Essential Functions• Establish and manage performance dashboards, analyze event triggers/alerts and determine appropriate follow up for Project Leader (PL) or other function(s) to act upon.• Coordinate project schedule and ensure timely updates of all key milestone and partner with PL on related calls.• Coordinate and support the risk and issue management process.• Manage all aspects of the Project Finances including Estimate at Completion (EAC), monthly expenses, invoices and reconciliation.• Demonstrate compliance with the Vendor and Purchase Order (PO) Management process.• Implement and maintain baseline and change control processes.• Ensure PL has timely and accurate data on areas including cost, schedule, scope, utilization, change orders and quality to support better decision-making.• Develop and maintain relevant sections of Project Management Plans.• Review and support project resource allocation within project budgeted for assigned portfolio/ projects.• Prepare correspondence, including meeting minutes, for project team and/or customer.• Organize and partner with PL in managing internal project team and customer meetings.• Prepare project status reports and presentation materials for internal project team and customer meetings.• Manage and coordinate core file reviews and support audits as needed. Drive e Trial Master File (eTMF) filing compliance focusing on completeness, timeliness and quality.• Manage project specific eTraining and oversee compliance.• Coordinate and support onboarding of new Key Project Team Members and system access.• Monitor project metrics and make required updates in IQVIA systems to ensure accurate and timely reporting is available to senior management.• Participate in regional initiatives to support Project Management Analyst (PMA) community and aid personal development. Qualifications• Bachelor's Degree Life sciences or other related field.• Typically requires +2 years of prior relevant experience.• Requires knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education.• Ideally, 1 year of relevant clinical research experience with analytical/financial skills or relevant Project Management experience or equivalent combination of education, training, and experience. Also, previous background in a consulting company is really useful. • Advanced level of English is mandatory, due to daily use #LI-NRJ #LI-Remote 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 EDC Data Acquisition Expert performs activities relating to the definition and implementation of Clinical Electronic Data Capture tools (EDC)  and related documents and processes aligned with Clinical Trial Protocol defined requirements for data capture. Activities are performed in close collaboration with Data Managers, Study Responsible Physicians (SRP), Study Responsible Scientists (SRS), and Biostatisticians. Responsibilities: Assess EDC collection requirements per protocol and create study start-up eCRF package based on global eCRF libraries.Design eCRF layout including form dynamics.Program Edit check and Custom Function.Create and configure tSDV technical specifications, Safety Gateway integration specifications and Datamart mapping specifications.Implement EDC coding configuration based on trial defined coding requirements.Perform test and Prod Rave EDC MigrationOversee planning, requirements, and implementation of IWRS integrations to EDC.Serve as subject matter expertise for complex elements of EDC database builds (including integrations).Serve subject matter expertise for complex elements of EDC database builds (including optimal custom functions implementation).Provide training to junior staff on EDC build and migration process and ToolsParticipate in process, system, and tool improvement initiatives within clinical data managementRequirements: Minimum of 5 years’ experience building EDC databases in support of clinical research.Technical EDC build experience in Medidata Rave implementing complex database builds.Demonstrated project management skills.Advanced Custom functions programming knowledge.Experience working on clinical trials.Experience working in highly diverse teams within clinical research; cross-functional, global, multiregional.Working knowledge of GCP/ICH guidelines.Knowledge of CDASHThis role is not eligible for UK visa sponsorship IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.• Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.• Assist with periodic review of study files for completeness.• Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.• Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.• May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training. Qualifications• High School Diploma or equivalent  Req• 3 years administrative support experience.• Equivalent combination of education, training and experience.• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.• Written and verbal communication skills including good command of English language.• Effective time management and organizational skills.• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.• Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.• Knowledge of applicable protocol requirements as provided in company training. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewPerform/Assist the Data Manager in managing various data management projects as per sponsor requirements and to provide efficient, quality management products. Support coordinate with other departments, sites and sponsors as and when necessary Essential Functions• Perform/Assist regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor.• Serve in the role of back-up to a Sr. Data Coordinator or Data Team Lead.• Manage the allocated tasks with minimum oversight.• Ensure that all the deliverables are of expected quality standards and meet customer expectations with support of Senior Data Manager.• Interact with Data Management team leaders to report on the quality of data collection and tasks done.• Attend internal study meetings and internal/ sponsor audits.• Assist in tracking and managing the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended by DTL.• Be compliant to trainings and eSOP reading.• Communication with Data Team Lead and other team members across functions should be collaborative. Qualifications• Bachelor's Degree Graduate Science/Bachelor Pharmacy or equivalent Pref• English Fluency Spoken and English• Basic computer applications like Microsoft excel, word, Inbox etc• Should have basic understanding of Drug development lifecycle and Overall Clinical research process 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 OverviewReview, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members. Essential Functions• To Prioritize and complete the assigned trainings on time.• Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.• To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information• determining initial/update status of incoming events• database entry• coding AE and Products, writing narratives, Literature related activities as per internal/ project  timelines.• Ensure to meet quality standards per project requirements.• Ensure to meet productivity and delivery standards per project requirements.• To ensure compliance to all project related processes and activities.• Creating, maintaining and tracking cases as applicable to the project plan.• Identify quality problems, if any, and bring them to the attention of a senior team member.• To demonstrate problem solving capabilities.• To mentor new teams members, if assigned by the Manager.• Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.• 100% compliance towards all people practices and processes• Perform other duties as assigned. Qualifications• High School Diploma or equivalent Scientific or healthcare discipline or allied life sciences Req• An Individual with a minimum of a Bachelor’s Degree in scientific or healthcare discipline or allied life sciences graduation with 1-1.5 years of relevant experience. Req• Good knowledge of medical terminology. Intermediate• Working knowledge of applicable Safety Database. Beginner• Knowledge of applicable global, regional, local clinical research regulatory requirements. Beginner• Excellent attention to detail and accuracy. Beginner• Good working knowledge of Microsoft Office and web-based applications. Beginner• Strong organizational skills and time management skills. Beginner• Strong verbal/written communication skills. Intermediate• Self-motivated and flexible. Intermediate• Ability to follow instructions/guidelines, utilize initiative and work independently. Intermediate• Ability to multi-task, manage competing priorities and deadlines. Beginner• Ability to delegate to less experienced team members. Beginner• Willingness and aptitude to learn new skills across Safety service lines. Beginner• Ability to establish and maintain effective communication and working relationships with coworkers, managers and clients. Beginner• Ability to work as a Team Player, contribute and work towards achieving Team goals. Beginner• Ensure quality of deliverables according to the agreed terms. Beginner• Demonstration of IQVIA core values while doing daily tasks Beginner• Extensive use of telephone and face-to-face communication requiring accurate perception of speech. Beginner• Regular sitting for extended periods of time. Beginner• May require occasional travel. Beginner• Flexibility to operate in shifts. Beginner 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.

Software Engineer (Vaadin / Java)Home-based/Remote We’re looking for a skilled and motivated Software Engineer to join our dynamic team and help shape the future of user interface development for our flagship products—such as IQVIA’s Health Data Research Platform, a key component of the Connected Health Platform. Key Responsibilities Enhance and maintain user interfaces for core applications, ensuring performance, usability, and scalability.Design, develop, test, and debug new UI features and components.Build and optimize the data transfer layer between frontend and backend systems.Collaborate on UI/UX planning through wireframes and design prototypes.Conduct code reviews and provide technical guidance to fellow UI developers.Write comprehensive unit and integration tests using JUnit and Mockito.Support user acceptance testing using Selenium WebDriver, Concordion, and Vaadin Testbench.Required Skills Vaadin Framework: Hands-on experience building rich web interfaces.Java: Strong object-oriented programming and clean coding practices.Spring Framework: Proficient in dependency injection and transaction management.Testing Tools: Skilled in JUnit and Mockito for automated testing.SQL: Solid understanding of relational databases and query optimization.Development Tools: Experience with IntelliJ IDEA, Git (GitLab), and Maven.Web Technologies: Familiarity with HTTP protocols and RESTful API design.What We Offer Flexible working hours (see 'Shift Timings')Both working options are possible: Hybrid (located in an IQVIA office) as well as fully remote.Collaborative and innovative work environmentOpportunities for professional growth and developmentCompetitive salary and benefits packageShift Timings Flexible working hours according to contract. Team core working time is between 10am and 4pm CET. The Ideal Candidate Will Also Have German language skills are an advantage but not required.Understanding of UX design principles.Experience with JPA/Hibernate, MSSQL-Server, Oracle, PostgreSQL.Familiarity with integrating applications to SSO solutions using OAuth2 or OIDC.Experience with browser automation using Selenium WebDriver.Test design experience with the Concordion framework or similar frameworks.Experience using AI-assisted software development tools such as GitHub Copilot, Cursor, or similar coding assistants.Skill Flexibility Experience with other UI frameworks like React.Experience in UI development for mobile applications.Familiarity with Windows or MacOS environments.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.

Provide medical expertise on pharmacovigilance services to all Quinties divisions as requested. The Director, Medical Safety participates in all aspects of Medical Safety’s involvement on assigned trials and stand-alone safety projects with appropriate oversight from management or more senior medical safety directors. The Director, Medical Safety also provides global project leadership on projects requiring multiple medical safety advisors and mentorship to junior medical safety staff. The Director, Medical Safety assists in the implementation of department missions, goals and objectives, oversight of operations, development of policies and procedures and standards for the department. 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 Provide 24×7 support for IQVIA’s enterprise network environment, encompassing complex WAN/LAN and in-house voice infrastructure. Responsibilities include configuring, monitoring, and troubleshooting network equipment such as Palo Alto Firewalls, Cisco SDWAN, routers, switches, wireless access points (WAPs), wireless LAN controllers (WLCs), Nexus switches, Cisco ACI, Cisco Voice (CUCM), Cisco ISE and F5 load balancers. Job Description: Strong knowledge of Cisco routing and switching technologies.Hands-on experience with Cisco SD-WAN and wireless solutions.Familiarity with network monitoring tools (DNAC, vManage, SolarWinds, NetFlow).Basic understanding of F5 load balancing and Cisco Voice.Intermediate knowledge of Palo Alto firewalls.Strong foundation in network protocols (TCP/IP, BGP, OSPF, VLANs).Experience working in an ITIL-governed environment, including change management processes.Familiarity with ServiceNow or similar ITSM/ticketing tools. Key Responsibilities Able to work with minimal or no Supervision post successful knowledge transfer.Manage and maintain enterprise network infrastructure, including LAN/WAN, routing, and switching environments.Implement and troubleshoot Cisco SD-WAN solutions, ensuring optimal performance and connectivity across sites.Deploy and support Cisco Wireless solutions, including configuration, optimization, and troubleshooting.Perform advanced troubleshooting for escalated network issues for faster resolution.Monitor and optimize network performance using enterprise tools such as Cisco DNA Center, vManage, NetFlow, and SolarWinds.Assist in new site builds and network expansions, including hardware installation, configuration, and testing.Configure and maintain F5 load balancers for basic add-on tasks and troubleshooting.Manage and troubleshoot Palo Alto firewalls at an intermediate level, ensuring compliance with security policies.Provide basic support for Cisco Voice systems, including call manager and VoIP troubleshooting.Maintain accurate network documentation, including diagrams, configurations, and change logs.Collaborate with cross-functional teams for network-related projects and incident resolution.Stay updated on emerging networking technologies and best practices to enhance operational efficiency.Ready to work in 24*7 Shift. 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.

Project Management Analysts are an integral part of the delivery of our clinical trials, working to bring drugs to market faster and ultimately improve patients’ lives. The Project Management Analyst (PMA) works in close partnership with the Project Leader, providing essential support in project management activities to mitigate risk, control cost, manage project schedule and ensure customer satisfaction related to assigned project/s.   The PMA is an entry level role for project management at IQVIA and you will work with cross functional teams across the global organization. The PMA typically works on project(s) which varies in scope and may also support a phase or portion of a large, complex project. IQVIA’s size and global footprint will present you with the breadth of opportunities necessary to develop your career. RESPONSIBILITIES Coordinate project schedules, estimates, cost control, risk management activities.Identify changes in scope and manage change control process.Manage monthly finance activities.Manage performance dashboards, analyze metrics, event triggers and alerts and determine appropriate follow up for Project Leader or others to act upon.Oversight of study files and support/manage study file reviews. Develop and maintain relevant sections of Project Execution Plans.Prepare correspondence, including meeting minutes, for study team and/or customer.Organize and support Project Leader in managing internal study team and customer meetings. Prepare presentation materials including study data for internal study team and customer meetings.Support audits and inspections.Analyze and manage resource requestsEnsure accurate and timely system updatesOversee vendor management activities as required REQUIRED KNOWLEDGE, SKILLS AND ABILITIES Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct is preferred.                                                Strong written and verbal communication skills including good command of English language                      Results-oriented approach to work delivery and output      Problem solving skills  Planning, time management and prioritization skills     Ability to handle conflicting priorities                                                                          Attention to detail and accuracy                                                                Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel, PowerPoint and MS Project        Ability to establish and maintain effective working relationships with coworkers, managers and clients                                                                   Ability to work across cultures and geographies with a high awareness and understanding of cultural differencesAbility to influence without authority                                                                 MINIMUM REQUIRED EDUCATION AND EXPERIENCE Bachelor's degree in life sciences or other related field and minimum of 1 year of clinical research, project management, analyst/finance, customer service experience with analytical/financial skills; or equivalent combination of education, training and experience.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.

Accurate Health Auditing & Consulting Single Member S.A., a company of the IQVIA Group and a leading Greek provider of medical audit, TPA and consulting services in the healthcare sector, operating both in Greece and abroad, is seeking administrative employees for its clinic offices within Private Hospitals, in Athens, in the context of cooperation with Insurance Companies and Insurance Funds. Position Highlights Be the polite face at patient reception and provide excellent patient serviceManage new Admissions, enter insured data, locate insured individuals through insurances systems (when required), and fill in relevant forms in the electronic systemNotify Insurance Companies of hospitalizations by electronically sending all relevant documents.Conduct daily reviews of aggregated case lists per HospitalCommunicate in detail the final opinion of the Medical Auditor to Insurance Companies and HospitalsCollaborate with medical staff to adhere to timelines and clinic workflowIssue guarantees for incidents where required.Handle email correspondence (with insurance companies and hospitals).Required Qualifications: University or Technological Educational Institute degreeExcellent knowledge of computer applications (Excel, Word, Outlook, Power Point) and Internet usageStrong written and oral communication skills, effective time management and teamwork abilities.Desired Qualifications: Health studies.Good knowledge of English.Previous experience in the healthcare industry, insurance market or consulting  services.What we offer: Salary based on qualificationsOpportunities for professional developmentIndefinite Contract (five-day, eight-hour employment) 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.

BIOAXIS Healthcare, an IQVIA business, the largest company that specializes in the provision of high-quality Patient Education and Care Services, through patient support programs, is seeking a dedicated and detail-oriented  Patient Support Coordination Manager to join our team. This role involves overseeing daily operations and ensuring compliance with industry standards while driving organizational excellence. Key Responsibilities: Daily Operations & Service Quality Oversee day-to-day service delivery to patients and healthcare professionals, ensuring high service quality and adherence to response time targets (SLAs).Monitor operational performance metrics and identify risks or delays, taking proactive action to resolve issues.Provide guidance to the coordination team, addressing questions, escalations, and operational challenges.Team Leadership & Scheduling Develop and manage the monthly shift schedule for the coordination team, ensuring adequate coverage based on business needs.Adjust the daily operational plan according to changing requirements, workload, and project-specific deadlines.Support team members by offering direction, clarifications, and coaching to ensure consistent performance.Process Optimization & Operational Excellence Assess existing workflows and recommend improvements to simplify procedures and increase overall efficiency.Implement and monitor corrective actions that enhance service quality and reduce operational gaps.Cross-Functional Collaboration Liaise with multiple internal departments (e.g., Sales, Quality, Medical, IT, Logistics) to ensure seamless operational execution.Ensure operational activities comply with internal standards, industry regulations and requirements.Qualifications required: Bachelor’s degree in business administration or a related field (e.g., Economics, Marketing).Proven experience in operations management, program supervision, or a related field.Data analysis and KPI monitoring skills, ensuring accurate measurement of performance indicators.Skills / Personality Strong organizational, problem-solving, and leadership skills.Strong interpersonal and collaboration skillsAbility to coordinate across departments and drive operational improvements.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.• Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.• Assist with periodic review of study files for completeness.• Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. Coordinate 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.• May collaborate with the clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.Qualifications• High School Diploma or equivalent Req• At least 1 year experience as CTA with Start Up responsibilities • Experience in RA and EC Submissions • Experience in EUCTR • Equivalent combination of education, training and experience.• Minimum one year clinical research experience strongly preferred.• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.• Written and verbal communication skills including good command of Greek and English language.• Effective time management and organizational skills.• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.• Basic knowledge of applicable clinical research regulatory requirement, 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™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Within our Sponsor dedicated model, our team contributes to the pipelines of the specific sponsor and therefore our CRAs are ‘indication and molecule experts’. We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study. Leadership recognises the skills, talent and experience of our clinical teams and strives to build upon this as the function evolves and grows. Our managers understand the sponsors priorities and the individual aspects of each model. Focus is given to career development from day one, including new hire orientation and onboarding, day to day problem solving and training and development. Additionally, IQVIA’s sponsor dedicated business works with the Sponsors SOP’s, creating more continuity for both parties. Our models offer excellent opportunities for experienced CRA’s to expand their knowledge and skills. IQVIA Belgium are currently seeking motivated Clinical Research Associate II practitioner to join our unique and dynamic Sponsor dedicated model. This is a role based in Belgium Your Role: Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesWork with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.Collaborate and liaise with study team members for project execution support as appropriate.If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.Your Profile: University degree in scientific discipline or health careMinimum of 18 months of independent, on-site monitoring experience as a CRA within a CRO or pharmaceutical environment.Excellent communication skills in Dutch, French, and English, both written and spoken.Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Organizational and problem-solving skills. Exceptional interpersonal and cross-cultural communication skills to build strong, trusted partnerships with Belgium site investigators and medical staff. A collaborative mindset to work effectively with cross-functional global teams, project managers, and local study coordinators.Why join us? Grow your career with access to development resources, training, and advancement opportunitiesEnjoy the flexibility and trust to balance your professional and personal commitmentsExpand your therapeutic knowledge through dedicated learning and development programsBe part of a successful global organization with an excellent reputation and supportive cultureBenefit from a company car, mobile phone, and an attractive rewards and benefits packageIQVIA 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.

Internal Job DescriptionIQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Within our Sponsor dedicated model, our team contributes to the pipelines of the specific sponsor and therefore our CRAs are ‘indication and molecule experts’. We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study. Leadership recognises the skills, talent and experience of our clinical teams and strives to build upon this as the function evolves and grows. Our managers understand the sponsors priorities and the individual aspects of each model. Focus is given to career development from day one, including new hire orientation and onboarding, day to day problem solving and training and development. Additionally, IQVIA’s sponsor dedicated business works with the Sponsors SOP’s, creating more continuity for both parties. Our models offer excellent opportunities for experienced CRA’s to expand their knowledge and skills. IQVIA Belgium are currently seeking motivated Senior Clinical Research Associate practitioner to join our unique and dynamic Sponsor dedicated model. This is a role based in Belgium Your Role: Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. Collaborate and liaise with study team members for project execution support as appropriate. If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Your Profile: University degree in scientific discipline or health care Minimum of 3 years of independent, on-site monitoring experience as a CRA within a CRO or pharmaceutical environment. Excellent communication skills in Dutch, French, and English, both written and spoken. Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Organizational and problem-solving skills. Exceptional interpersonal and cross-cultural communication skills to build strong, trusted partnerships with Belgium site investigators and medical staff. A collaborative mindset to work effectively with cross-functional global teams, project managers, and local study coordinators. Why join us? Grow your career with access to development resources, training, and advancement opportunities Enjoy the flexibility and trust to balance your professional and personal commitments Expand your therapeutic knowledge through dedicated learning and development programs Be part of a successful global organization with an excellent reputation and supportive culture Benefit from a company car, mobile phone, and an attractive rewards and benefits package 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 Location: Bheemavaram Job OverviewMaximize sales growth in a specified geographical territory, consistent with Company strategy and objectives. This is generally achieved by educating and informing physicians and/or hospital staff on the features and benefits the customer’s product(s) versus competitor products in order to increase prescriptions and/or use by the healthcare professionals. Essential Functions• Achieve assigned activity goals and targets for the territory as agreed with the reporting manager, with an initial high level of supervision and coaching provided by the company, customer and manager.• Conduct sales interviews, carry out pre-call planning and preparation and develop a self analytical approach in order to identify learning areas from each call.• Promote and sell customer’s therapeutic products to general practitioners, other identified healthcare providers, and/ or other healthcare professionals in the retail market.• Within a specific geographical territory, identify target customers while maintaining and analyzing customer records.• Maintain records in the reporting systems within the required timescales.• Effectively utilize the relevant software (e.g. Electronic Territory Management System, CRM systems) to maintain records updated and to report daily calls.• Organize and hold group events to optimize business while complying with relevant country legislation.• Keep Line Manager informed about changes in competitor activities and other market changes.• Maintain an up-to-date sales / technical knowledge of specialty and disease areas and relevant publications as per customer profile.• Keep all Company equipment safe and in a good state of repair.• Share experiences, ideas and techniques in order to assist with the sales training of colleagues.• Discuss, agree and document assigned activity, Key Performance Indicator tools, and targets as agreed with Line Manager.• Successfully complete career development courses and additional training as required by the customer.• Ensure the reporting of any identified Adverse Events in line with prevailing process and guidelines.• Project a professional impression of the Company and act in accordance with the relevant Pharmaceutical Industry’s Code of Practice• Perform other duties as assigned. Qualifications• High School Diploma or equivalent 5 years’ relevant experience Req Or• Bachelor's Degree Life Sciences or related field Req• Equivalent combination of education, training and experience may be accepted in lieu of educational requirements Req• Basic knowledge of Pharma Market and related procedures.• Fluency software operating systems, such as MS Office and customer relationship management systems.• Effective verbal and written communication skills.• Ability to conduct face to face presentations to customers.• Ability to prioritize and coordinate multiple work requirements to meet deadlines.• Ability to establish and maintain effective working relationships with co-workers, managers and clients.•  Make plans to obtain any industry qualifications essential to function as a Medical Representative in the relevant market.  Req• AZDL  - Driver Licence - Valid And In State   Req IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Field Sales Associate – UrologyAbout the Role As a Field Sales Associate (FSA) at Boston Scientific, you will play a pivotal role in supporting regional accounts under the guidance of the Region Sales Manager. Working closely with Territory Managers, you’ll help maintain market share across existing accounts while delivering exceptional service and clinical support. This includes conducting in-services and assisting with training initiatives to elevate the team’s performance and customer experience. Key Responsibilities Strengthen key account relationships through regular customer visits, product demonstrations, educational programs, in-services, procedural observation, and issue resolutionEngage with a broad range of stakeholders including physicians, nurses, technicians, materials management, hospital administration, and infection controlCollaborate with Territory Managers, Sales Management, HEMA, and cross-functional teams to assess business conditions and sales trendsDrive utilization of targeted technologies across assigned accountsDemonstrate clinical excellence in relevant disease statesDevelop and execute proactive service plans with the Region Manager and team to maintain market share and enhance customer satisfactionSupport professional education initiatives by participating in on-site and field training workshopsIdentify opportunities to present Boston Scientific solutions that drive regional sales activityProvide timely updates to the Regional Manager on business plans, competitive landscape, and industry trendsManage expense and promotional budgets in accordance with company guidelinesPrepare comprehensive account-level plans aligned with the Urology Division’s strategic goalsLeverage sales enablement tools such as Salesforce and Tableau to optimize performanceMaintain accurate records of expenses, customer interactions, and field reportsSubmit all required administrative documentation promptlyConduct all sales activities in compliance with Travel & Entertainment (T&E) guidelines, AdvaMed policies, and company integrity standardsParticipate in occasional weekend and evening trade shows or meetingsCommit to travel requirements, typically 40–50%Preferred Qualifications Self-starter with strong leadership qualities and high coachabilityProven ability to set priorities and manage time effectivelySkilled in building and maintaining customer relationshipsFlexible and adaptable to change; able to align work with strategic goalsEnergetic, enthusiastic, goal-oriented, and determinedThrives in a fast-paced, competitive environmentRequired Qualifications Minimum 1 year of successful B2B sales experienceCompletion of a formal sales training program or relevant degreeBachelor’s degreeMust reside within the assigned territoryNote: This role is not eligible for visa sponsorship. Candidates must have authorization to work in the US without the need for sponsorship.#LI-CESIQVIA 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 70-75,000 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.

Recruiter – Clinical Talent Acquisition Sao Paulo (Brazil) | Hybrid Job OverviewPartner with hiring managers and business leaders to deliver full-cycle recruitment for clinical roles across Latin America, with primary focus on Brazil, Argentina, Mexico, and Colombia. Contribute to the continuous improvement of Talent Acquisition programs, processes, and talent attraction strategies while ensuring an exceptional candidate and stakeholder experience. Essential Functions Manage the full recruitment lifecycle for clinical positions, including intake meetings, sourcing strategy development, talent mapping, candidate assessment, interview management, offer negotiation, and onboarding support.Develop and execute innovative sourcing strategies to identify and attract high-quality clinical talent through multiple channels, including social media, professional networks, referrals, and direct sourcing techniques.Build and maintain proactive talent pipelines for current and future hiring needs across multiple clinical functions and geographies.Represent the organization at career fairs, industry events, university partnerships, and other talent attraction initiatives to strengthen employer brand awareness.Partner with hiring managers as a trusted advisor by providing insights on labor market conditions, talent availability, compensation trends, and competitive intelligence.Ensure compliance with local employment laws, global hiring policies, diversity and inclusion objectives, and applicant tracking system requirements.Collaborate closely with HR Business Partners, Compensation, and business leaders to facilitate hiring decisions and offer recommendations.Analyze recruitment metrics and market data to identify trends, drive continuous improvement, and support workforce planning initiatives.Contribute to employer branding, candidate engagement, and Talent Acquisition projects at the local, regional, and global levels.Qualifications: Bachelor’s degree preferred or equivalent experience2 years of job experience in a Talent Acquisition/HR function, or an equivalent combination of education, training, and experience.Experience in recruiting, talent acquisition, or human resources, preferably supporting clinical, healthcare, life sciences, CRO, or related professional hiring highly desiredFluency in Portuguese and English (written and verbal) required.Spanish proficiency is highly desirable.Strong proficiency in Microsoft Office and digital tools (Workday or similar ATS are a plus).High attention to detail, strong organizational abilities, and the ability to manage multiple priorities effectively.Strong problem‑solving skills.Strong customer‑service mindset and ability to work collaboratively with hiring managers and cross‑functional teams.High level of discretion and professionalism when handling confidential information.Good understanding of local employment legislation and compliance throughout the hiring process.Why you’ll love working in this team Enjoy flexibility through a hybrid work model with one day per week in the office.Join a collaborative, high-performing Talent Acquisition team that values learning, innovation, and partnership.Support hiring initiatives across multiple LATAM markets while expanding your knowledge of clinical research and healthcare industries.Gain exposure to regional and global Talent Acquisition projects that drive meaningful business impact.Play a key role in connecting talented professionals with opportunities that help advance healthcare worldwide.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.

Localização: São Paulo/SP (Híbrido) Buscamos um(a) profissional com perfil analítico para atuar na gestão e otimização da jornada do cliente, transformando dados em insights que apoiem decisões estratégicas e aumentem o engajamento em canais digitais e presenciais.  Principais responsabilidades:    • Analisar KPIs e métricas de performance omnichannel.    • Desenvolver dashboards e relatórios gerenciais.    • Identificar oportunidades de melhoria na jornada do cliente.    • Apoiar times de Marketing, Customer Experience e Tecnologia na definição de estratégias de engajamento.    • Conduzir análises de dados e apresentar recomendações para diferentes stakeholders.     Requisitos:    • Ensino superior completo em Administração, Marketing, Engenharia, Estatística, Ciência de Dados ou áreas correlatas.    • Experiência em funções analíticas, CRM, Customer Engagement ou Omnichannel.    • Conhecimento em Power BI, Tableau ou ferramentas similares.    • Inglês avançado.    • Experiência na indústria farmacêutica ou healthcare será um diferencial.    Competências desejadas: Capacidade analítica, comunicação, organização, visão de negócio, proatividade e habilidade para atuar em ambientes multidisciplinares. 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 #LI-LATAM 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.

Rattachement hiérarchique Le poste est rattaché à la Direction de RCA Factory, agence du Groupe IQVIA, et travaille en lien étroit avec les équipes commerciales, conseil, opérations, finance, administration des ventes et les interlocuteurs du groupe, y compris dans un environnement international. Finalité du poste L’Assistant(e) de Direction assure un rôle central de support administratif, commercial et organisationnel au sein de RCA Factory, Groupe IQVIA.Il/elle contribue au bon fonctionnement quotidien de l’agence, au suivi des processus commerciaux, à la gestion administrative des dossiers clients et au support opérationnel d’activités associatives, notamment dans l’écosystème santé et data. Missions principales 1. Support administratif et commercial Établir, mettre en forme et transmettre les devis clients dans le respect des procédures internes de RCA Factory et du Groupe IQVIA.Assurer le suivi des devis émis, des bons de commande, des contrats clients et des documents administratifs associés.Coordonner les échanges avec les équipes internes afin de garantir l’avancement des dossiers commerciaux.Relancer les parties prenantes internes et externes pour sécuriser les échéances et fluidifier le cycle de validation.Veiller à la conformité, à l’exhaustivité et à la bonne traçabilité des documents commerciaux.Participer à l’amélioration continue des processus administratifs liés au cycle de vente.Être en mesure d’échanger en anglais avec certains interlocuteurs internes du Groupe IQVIA, le cas échéant.2. Gestion et suivi des opportunités dans Salesforce Saisir les opportunités commerciales dans Salesforce / SFDC, selon les standards et procédures du Groupe IQVIA.Mettre à jour les informations relatives aux opportunités : statut, montant, échéances, documents associés, interlocuteurs, étapes de validation et prévisions.Assurer la fiabilité et la complétude des données renseignées dans l’outil CRM.Collaborer avec les équipes commerciales et opérationnelles afin de garantir un suivi rigoureux du pipeline et des dossiers en cours.Contribuer à la bonne visibilité de l’activité commerciale de l’agence à travers la mise à jour régulière des informations dans les outils internes.3. Support administratif d’une association loi 1901 Assurer la gestion administrative courante de l’association Healthcare Data Institute.Suivre les cotisations des membres (émission, relances et mise à jour des informations).Participer au suivi comptable de premier niveau.Préparer et diffuser les documents de présentation de l’association.Contribuer à l’onboarding des nouveaux membres.Mettre à jour les outils de suivi et assurer l’interface avec les membres, partenaires et prestataires.4. Suivi administratif interne Assurer le suivi des récupérations et des absences spécifiques des collaborateurs, selon les règles internes applicables.Mettre à jour les tableaux de suivi RH ou administratifs correspondants.Veiller à la bonne circulation de l’information entre les collaborateurs, les managers et les services concernés.Participer à la coordination administrative des sujets internes de l’agence.5. Organisation des déplacements professionnels Organiser les déplacements professionnels des collaborateurs de RCA Factory  : réservations de transport, hôtels et prestations associées.Veiller au respect des contraintes de planning, des budgets et des politiques internes du Groupe IQVIA.Assurer le suivi administratif des réservations, confirmations, modifications et justificatifs.Gérer les éventuels ajustements, annulations ou urgences liés aux déplacements.Être en capacité d’interagir avec des prestataires ou plateformes de réservation en français comme en anglais.Activités transverses Préparer, mettre à jour et suivre différents tableaux de bord administratifs et commerciaux.Classer, archiver et organiser les documents selon les procédures internes.Assurer une communication fluide avec les interlocuteurs internes et externes, en français et ponctuellement en anglais.Contribuer au respect des échéances administratives, commerciales et contractuelles.Participer à la qualité du service rendu aux équipes, clients, membres et partenaires.Apporter un soutien opérationnel à la Direction et aux équipes dans la gestion quotidienne de l’agence.Profil recherché Formation Formation de type Bac+2 à Bac+3 en assistanat de direction, gestion administrative, gestion PME-PMI, commerce, administration des ventes ou équivalent.Une expérience dans un environnement agence, conseil, santé, data, services B2B ou groupe international est appréciée.Expérience Expérience réussie en assistanat de direction, assistanat administratif, assistanat commercial ou administration des ventes.Expérience dans le suivi de devis, bons de commande, contrats clients et processus de facturation appréciée.La maîtrise ou la pratique de Salesforce / SFDC constitue un atout important.Une connaissance du fonctionnement d’une association loi 1901 serait un plus.Une expérience dans un environnement international ou matriciel serait appréciée.Compétences techniques Très bonne maîtrise des outils bureautiques : Excel, Word, PowerPoint et Outlook.Connaissance de Salesforce / SAP souhaitée.Capacité à gérer des tableaux de suivi et à fiabiliser des données administratives ou commerciales.Bonne compréhension des processus administratifs, commerciaux et contractuels.Aisance avec les outils collaboratifs et les environnements digitaux.Capacité à travailler dans le respect de procédures internes structurées.Anglais professionnel requis, à l’écrit comme à l’oral, pour interagir avec certains interlocuteurs internes, outils, documents ou process du Groupe IQVIA.Qualités personnelles Rigueur, fiabilité et sens de l’organisation.Capacité à gérer plusieurs sujets en parallèle et à prioriser les urgences.Excellent relationnel et sens du service.Discrétion et respect de la confidentialité.Autonomie, réactivité et esprit d’initiative.Bonne communication écrite et orale, en français comme en anglais professionnel.Capacité à travailler avec des interlocuteurs variés : direction, équipes commerciales, consultants, fonctions support, clients, membres et partenaires.Environnement du poste Le poste s’inscrit au sein de RCA Factory, Groupe IQVIA, dans un environnement exigeant, dynamique et orienté santé, data et services aux acteurs de l’écosystème santé. L’Assistant(e) de Direction joue un rôle clé dans la coordination administrative de l’agence, la sécurisation des processus commerciaux et contractuels, le support aux équipes et la fluidité du fonctionnement quotidien. La pratique de l’anglais est nécessaire pour évoluer efficacement dans l’environnement international du Groupe IQVIA. 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.

【会社紹介・ビジョン】  私たちIQVIAは、ヒューマンデータサイエンスの先駆的な企業として、医療・ヘルスケアの前進に取り組む皆様をIQVIAならではの革新的なソリューションによってご支援することで、「誰もが、より健康に自分らしく生きられる社会」の実現を目指しています。世界最大規模を誇る医療・ヘルスケア関連データを基盤に、人・データ・サイエンスを融合させた見地から、未だ満たされない治療ニーズに応える、新たな医薬品や医療機器の開発と市販化、厳格化する規制やコンプライアンスへの対応、持続可能な医療システム推進の支援など、患者さんをはじめとするすべての人々のために、より良い未来へと医療・ヘルスケアを前進させていく力となることが、私たちの使命です。  世界100以上の国と地域で約9万人が活動するIQVIAの日本法人として、IQVIAジャパンでは約6,000人が一丸となり、この使命に向かって日々、力を尽くしています。    （部門） 内科、循環器内科、消化器内科、神経内科、総合診療科、一般外科、胸部外科、乳腺外科、免疫アレルギー、産婦人科、精神科などの専門分野を有して いるドクターが在籍しています。 さらに各種がん医療に精通した医師が多いことも特徴です。 業務内容 メディカルモニタリング：日本に割り当てられたプロジェクトのメディカルアドバイザーとして以下の役割を担う ・プロトコルの明確化、組入れ基準の決定、患者さんの安全性・適格性の問題を含むプロトコル関連の問題について、プロジェクトメンバーや治験実施医療機関に対し医学的アドバイスを行う ・プロトコル、治験薬概要書、症例報告書の医学的レビューを行う ・プロジェクトチームに対し、疾患領域や適応症に関するトレーニングを提供する ・インヴェスティゲーター・ミーティングに参加する ・有害事象のレビューを行う ・ファーマコビジランス部門と協力して、重篤な有害事象のレビューを行う ・ファーマコビジランス部門と協力し、またはその代理として、累積/類似症例の分析をサポートする ・有害事象コーディングの医学的レビューを行う ・総括報告書とナラティブのレビューを行う ・キックオフミーティング、チームミーティング、クライアントミーティングに参加する ・就業時間以外にプロトコル関連する緊急問題が生じた場合は所定のルールに従ってタイムリーに対応する 候補者要件 【必須】 ・日本における医師免許・4年以上の臨床経験（研修期間含む）と、オンコロジー経験 ＊腫瘍内科経験 ・リモートワークに懸念がない方 (English )Candidates must hold a valid Japanese medical license and have experience in Medical Oncology.・語学力 > 日本語：あらゆるコミュニケーションの場面におけるビジネスレベルの能力 >英語：読む・書くについてビジネスレベルの能力。および、聞く・話すについて日常会話が可能であり、就業後に能力を向上する意欲があること 【尚可の条件】 英語：あらゆるコミュニケーションの場面におけるビジネスレベルの能力。   勤務時間 原則フルタイム(7.5hour/day フレックスタイム適用) 曜日限定勤務などは応相談   勤務地 ・自宅/リモートベース 出社が必要な際には対応できる方 勤務時間 原則フルタイム(7.5hour/day フレックスタイム適用) 曜日限定勤務などは応相談（週一日は臨床業務希望など）   勤務地 ・東京、大阪、福岡 【雇用形態・勤務時間・福利厚生・休日休暇】  雇用形態：正社員／契約社員など  勤務時間：9:00-17:30 フレックス勤務：あり  在宅勤務制度：あり 福利厚生：法定内（社会保険制度）・法定外（IQVIA独自制度）の両面から充実した福利厚生制度あり  受動喫煙対策：あり  休日休暇：年次有給休暇、夏季休暇、病気休暇、特別休暇、女性特別休暇、育児介護休暇、看護休暇·など  試用期間：あり（通常６か月）  【給与・待遇】  給与：当社規定により優遇します  昇給：あり  賞与：あり  時間外手当：あり  【選考プロセス】  書類選考→部門面接2回 ＊必要に応じ人事面談を挟みます。 【応募方法】  日本語の履歴書、職務経歴書をお送りください。 紹介会社様へ： ご紹介の際には、現在の副業状況、今後の希望についても ご記載ください。 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.