IQVIA

About the Team / DepartmentYou will join a global Project Management team supporting Linguistic Validation (LV) and eCOA projects for clinical trials. The team works closely with internal stakeholders, clients, and external vendors to deliver high-quality, compliant, patient-facing materials across multiple regions and languages. Job OverviewManages the operational aspects of projects and programs. Will ensure that all project work is completed in accordance with SOPs, policies and practices. Essential Functions Why Join This RoleThis role offers strong exposure to global projects and cross-functional collaboration in a dynamic environment. You will develop end-to-end project management skills, build stakeholder relationships, and gain valuable experience in clinical trial delivery, with clear opportunities for career progression into senior or program management roles. Essential Functions• Create, track and report on project timelines• Manage project budgets and approval of invoices• Produce and distribute status, tracking and financial reports for internal and external team members and senior management.• Prepare and present project information at internal and external meetings.• May be assigned responsibility for sub-projects or specific components of the project or program• May participate in proposal development and sales/proposal presentations• Coordinate with other project resources within and outside the organization.• Provide input into project proposals and RFPs.• Ensure that work is conducted in compliance with standard processes, policies and procedures and meets project timeline metrics.• Serve as a backup contact for internal Project Managers.• Identify and negotiate out of scope project work• Responsibility for financial reporting on the project including tracking deliverables and invoicing• Meet with team members on a regular basis regarding project tasks to ensure project milestones are met.• Partner with other Project Managers to develop and implement process improvements Qualifications• Bachelor's Degree  Req• 3 years of related experience Req Or• Equivalent combination of education, training and experience Req• Strong communication and interpersonal skills• Good problem solving skills• Demonstrated ability to deliver results to the appropriate quality and timeline metrics• Good teamwork skills• Excellent customer service skills• Ability to work under limited direction• Strong software and computer skills, including MS Office applications• Ability to establish and maintain effective working relationships with coworkers, managers and clients IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Mitarbeiter Belegvorbereitung/ Poststelle in Taucha (m/w/d) -flexibles Schichtsystem Die IQVIA Health System Services GmbH, ehemals DAVASO GmbH, ist führender Dienstleister für das Genehmigungs- und Abrechnungsmanagement gesetzlicher Krankenkassen und Technologieanbieter für Softwarelösungen mit Schwerpunkt der digitalen Transformation unserer Kundenprozesse, unter anderem in den Bereichen Datenerfassung und -verarbeitung, Image Processing sowie Analyse und Datensauswertungsarbeiten. Ebenso beinhaltet das Produkt- und Dienstleistungsportfolio IT-Lösungen für das Gesundheitswesen, Finanzdienstleister sowie Industrie- und Handelskammern. Das Unternehmen ist Teil von IQVIA, einem führenden, globalen Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung für Life Science Unternehmen. Mit über 35 Jahren Markterfahrung agieren die über 1.300 Mitarbeitenden an den Standorten Leipzig, Dortmund und Taucha sowie standortübergreifend. Aufgaben: -Dein Aufgabengebiet umfasst die Annahme und Vorbereitung der Eingangspost sowie die Erfassung und Dokumentation der jeweils erhaltenen Postvolumina in Brief- und Paketform. -Der Aufgabenbereich beinhaltet zudem körperliche Tätigkeiten wie das Schieben von Postwagen. -Routiniert erledigst Du die Fein- und Grobsortierung der Post nach Empfänger im Unternehmen und verteilst diese über die vorgegebenen Postwege. -Zudem bist Du für die Bearbeitung des Postausgangs sowie für die Übergabe der Ausgangspost an die jeweiligen Postdienstleister zuständig. -Du bist ebenfalls für die Aufbereitung & Transporte des Beleggutes innerhalb des Standortes mittels Wagen verantwortlich. -Des Weiteren gehört die Archivierung sowie die Vernichtung der gescannten Dokumente zu Deinen Aufgaben. Voraussetzungen: -Du bist bereit, in einem 2- oder 3-Schichtsystem zu arbeiten -Die Frühschicht findet von 05:00 bis 13:30 Uhr statt, die Spätschicht von 13:00 bis 21:30 Uhr und die Nachtschicht von 21:00 bis 05:30 Uhr (zzgl. 25 % Zuschlag). -Zuverlässige Teilnahme an allen vorgesehenen Schichten gemäß Einsatzplanung -Du hast den Blick fürs Detail und erledigst deine Aufgaben präzise und mit Sorgfalt. -Deine Aufgaben organisierst du selbstständig und zielstrebig, dabei unterstützt ihr euch im Team gegenseitig. -Durch deine rasche Auffassungsgabe gelingt es dir verschiedenste Unterlagen und Belege verantwortungsvoll zu bearbeiten. -Du möchtest mindestens 35 oder 40 Wochenstunden vor Ort in Taucha tätig sein. -Sowohl Berufserfahrene (zum Beispiel auf dem Produktionsgewerbe) als auch Quereinsteiger und Neueinsteiger sind bei uns willkommen. Das erwartet dich: -Mindesteinstiegslohn 14,50 €/ Stunde (bei Vollzeit 2514,00 € / Monat) -Leistungsbezogener monatlicher Bonus von bis zu 3120,00 € jährlich (bei Vollzeit 260,00 € / Monat) -Nachtschichtzuschlag in Höhe von 25% ab der 1.Stunde -Durch unsere Trainer- und Mentorenprogramm ist eine strukturierte Einarbeitung garantiert und Du bekommst regelmäßiges wertvolles Feedback -Es gibt eine faire Überstundenregelung mit Freizeitausgleich oder einer Vergütungsmöglichkeit (25 % Zuschlag bei Vollzeitbeschäftigung) -Du kannst interne Entwicklungsmöglichkeiten, wie individuelle Weiterbildungen, Workshops und Seminare nutzen sowie eigene Seminarwünsche einbringen -Unsere Mitarbeiterversorgung bietet kostengünstiges Essen u.a. warmes Mittagessen für 1,30 € -kostenlose Kalt- und Heißgetränke, sowie auch kostenloses Obst für alle Beschäftigten -Viele Rabatte/ Angebote durch Mitgliedschaft bei corporate benefits -Betriebliche Altersvorsorge -kostenlose Lebensberatung von TALINGO EAP -betriebliches Gesundheitsmanagement -kostengünstiger Parkplatz -rabattiertes Jobticket -regelmäßige Unternehmensevents wie u.a. Grillfeste Werde Teil unseres Teams und freue Dich auf ein dynamisches Umfeld und spannende Aufgaben. Wir schätzen Vielfalt und begrüßen daher alle Bewerbungen – unabhängig von Geschlecht, Nationalität, ethnischer und sozialer Herkunft, Religion/Weltanschauung, Behinderung, Alter sowie sexueller Identität. Bewerbungen gerne auch per Mail an: [email protected] 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.

Sachbearbeiter (m/w/d) für die Datenerfassung- flexibles Schichtsystem- hybrid Homeoffice möglich Die IQVIA Health System Services GmbH, ehemals DAVASO GmbH, ist führender Dienstleister für das Genehmigungs- und Abrechnungsmanagement gesetzlicher Krankenkassen und Technologieanbieter für Softwarelösungen mit Schwerpunkt der digitalen Transformation unserer Kundenprozesse, unter anderem in den Bereichen Datenerfassung und -verarbeitung, Image Processing sowie Analyse und Datensauswertungsarbeiten. Ebenso beinhaltet das Produkt- und Dienstleistungsportfolio IT-Lösungen für das Gesundheitswesen, Finanzdienstleister sowie Industrie- und Handelskammern. Das Unternehmen ist Teil von IQVIA, einem führenden, globalen Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung für Life Science Unternehmen. Mit über 35 Jahren Markterfahrung agieren die über 1.300 Mitarbeitenden an den Standorten Leipzig, Dortmund und Taucha sowie standortübergreifend. Aufgaben: -Du bist verantwortlich für das Erfassen und Bearbeiten von digitalisierten Daten im Gesundheitswesen in unserer hauseigenen Systemsoftware. -Du klassifizierst das Beleggut in Rechnungen, Verordnungen und sonstige Anlagen. -Die Erstellung eines Datensatzes anhand des eingereichten Belegguts gehört ebenfalls zu Deinen Aufgaben. -Letztlich gehört die Kontrolle der Daten und die Markierung von Auffälligkeiten und Abweichungen zu Deinen Aufgaben. Voraussetzungen: -Du bist bereit, in einem 2- oder 3-Schichtsystem zu arbeiten -Die Frühschicht findet von 05:00 bis 13:30 Uhr statt, die Spätschicht von 13:00 bis 21:30 Uhr und die Nachtschicht von 21:00 bis 05:30 Uhr (zzgl. 25 % Zuschlag). -Zuverlässige Teilnahme an allen vorgesehenen Schichten gemäß Einsatzplanung -Du verfügst über erste Berufserfahrungen im kaufmännischen Bereich. -Du zeichnest dich durch eine genaue, systematische, zügige und selbstständige Arbeitsweise aus. -Du bist verantwortungsbewusst, teamfähig und zeichnest dich durch eine sorgfältige und konzentrierte Arbeitsweise aus. -Ein sicherer Umgang mit MS-Office-Produkten und die Beherrschung des Nummernblocks, sowie der sichere Umgang der Tastatur sind wünschenswert. Das erwartet dich: -Mindesteinstiegslohn 14,50 €/ Stunde (bei Vollzeit 2514,00 € / Monat) -Leistungsbezogener monatlicher Bonus von bis zu 3120,00 € jährlich (bei Vollzeit 260,00 € / Monat) -Nachtschichtzuschlag in Höhe von 25% ab der 1.Stunde -Durch unsere Trainer- und Mentorenprogramm ist eine strukturierte Einarbeitung garantiert und Du bekommst regelmäßiges wertvolles Feedback -Es gibt eine faire Überstundenregelung mit Freizeitausgleich oder einer Vergütungsmöglichkeit (25 % Zuschlag bei Vollzeitbeschäftigung) -Du kannst interne Entwicklungsmöglichkeiten, wie individuelle Weiterbildungen, Workshops und Seminare nutzen sowie eigene Seminarwünsche einbringen -Unsere Mitarbeiterversorgung bietet kostengünstiges Essen u.a. warmes Mittagessen für 1,30 € -kostenlose Kalt- und Heißgetränke, sowie auch kostenloses Obst für alle Beschäftigten -Viele Rabatte/ Angebote durch Mitgliedschaft bei corporate benefits -Betriebliche Altersvorsorge -kostenlose Lebensberatung von TALINGO EAP -betriebliches Gesundheitsmanagement -kostengünstiger Parkplatz -rabattiertes Jobticket -regelmäßige Unternehmensevents wie u.a. Grillfeste Werde Teil unseres Teams und freue Dich auf ein dynamisches Umfeld und spannende Aufgaben. Wir schätzen Vielfalt und begrüßen daher alle Bewerbungen – unabhängig von Geschlecht, Nationalität, ethnischer und sozialer Herkunft, Religion/Weltanschauung, Behinderung, Alter sowie sexueller Identität. Bewerbungen gerne auch per Mail an: [email protected] 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.

Mitarbeiter Urbelegebearbeitung (Urbelegeabgleich) (m/w/d)- flexibles Schichtsystem- hybrid Homeoffice möglich Die IQVIA Health System Services GmbH, ehemals DAVASO GmbH, ist führender Dienstleister für das Genehmigungs- und Abrechnungsmanagement gesetzlicher Krankenkassen und Technologieanbieter für Softwarelösungen mit Schwerpunkt der digitalen Transformation unserer Kundenprozesse, unter anderem in den Bereichen Datenerfassung und -verarbeitung, Image Processing sowie Analyse und Datensauswertungsarbeiten. Ebenso beinhaltet das Produkt- und Dienstleistungsportfolio IT-Lösungen für das Gesundheitswesen, Finanzdienstleister sowie Industrie- und Handelskammern. Das Unternehmen ist Teil von IQVIA, einem führenden, globalen Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung für Life Science Unternehmen. Mit über 35 Jahren Markterfahrung agieren die über 1.300 Mitarbeitenden an den Standorten Leipzig, Dortmund und Taucha sowie standortübergreifend. Aufgaben: -Du bist verantwortlich für die Formalienprüfung von Abrechnungen mit Kennzeichnung von Auffälligkeiten im Rahmen der Prüfaufträge für den Bereich Leistungsabrechnung gemäß § 302 SGB V bei gleichzeitiger Kontrolle auf Datenlieferung. -Du pflegst bzw. erfässt standardisierte Vorlagen mit Fachinformationen. -Darüber hinaus bearbeitest du Vorgänge, die zum Weiterversand an den Kostenträger bzw. zur Rücksendung an den Abrechner vorgesehen sind. -Zu deinen Aufgaben gehört weiterhin die Bearbeitung von Vorgängen zur Weiterleitung an die manuelle Rechnungs- und Verordnungserfassung. Voraussetzungen: -Du bist bereit, in einem 2- oder 3-Schichtsystem zu arbeiten -Die Frühschicht findet von 05:00 bis 13:30 Uhr statt, die Spätschicht von 13:00 bis 21:30 Uhr und die Nachtschicht von 21:00 bis 05:30 Uhr (zzgl. 25 % Zuschlag). -Zuverlässige Teilnahme an allen vorgesehenen Schichten gemäß Einsatzplanung -Du verfügst über erste Berufserfahrungen im kaufmännischen Bereich. -Du zeichnest dich durch eine genaue, systematische, zügige und selbstständige Arbeitsweise aus. -Du bist verantwortungsbewusst, teamfähig und zeichnest dich durch eine sorgfältige und konzentrierte Arbeitsweise aus. -Ein sicherer Umgang mit MS-Office-Produkten und die Beherrschung des Nummernblocks, sowie der sichere Umgang der Tastatur sind wünschenswert. Das erwartet dich: -Mindesteinstiegslohn 14,50 €/ Stunde (bei Vollzeit 2514,00 € / Monat) -Leistungsbezogener monatlicher Bonus von bis zu 3120,00 € jährlich (bei Vollzeit 260,00 € / Monat) -Nachtschichtzuschlag in Höhe von 25% ab der 1.Stunde -Durch unsere Trainer- und Mentorenprogramm ist eine strukturierte Einarbeitung garantiert und Du bekommst regelmäßiges wertvolles Feedback -Es gibt eine faire Überstundenregelung mit Freizeitausgleich oder einer Vergütungsmöglichkeit (25 % Zuschlag bei Vollzeitbeschäftigung) -Du kannst interne Entwicklungsmöglichkeiten, wie individuelle Weiterbildungen, Workshops und Seminare nutzen sowie eigene Seminarwünsche einbringen -Unsere Mitarbeiterversorgung bietet kostengünstiges Essen u.a. warmes Mittagessen für 1,30 € -kostenlose Kalt- und Heißgetränke, sowie auch kostenloses Obst für alle Beschäftigten -Viele Rabatte/ Angebote durch Mitgliedschaft bei corporate benefits -Betriebliche Altersvorsorge -kostenlose Lebensberatung von TALINGO EAP -betriebliches Gesundheitsmanagement -kostengünstiger Parkplatz -rabattiertes Jobticket -regelmäßige Unternehmensevents wie u.a. Grillfeste Werde Teil unseres Teams und freue Dich auf ein dynamisches Umfeld und spannende Aufgaben. Wir schätzen Vielfalt und begrüßen daher alle Bewerbungen – unabhängig von Geschlecht, Nationalität, ethnischer und sozialer Herkunft, Religion/Weltanschauung, Behinderung, Alter sowie sexueller Identität. Bewerbungen gerne auch per Mail an: [email protected] 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.

Manila Speaker Bureau Logistics Planner IQVIA’s Speaker Bureau team consists of dedicated meeting professionals who plan and manage highly compliant meetings and events for Life Sciences organizations.  We work with our clients to deliver a high-quality attendee experience through a range of in-person, hybrid, and virtual meetings by seamlessly pairing deep industry expertise, best-in-class compliance technology and an innovative, scalable approach to support our client’s Speaker Bureau.  The Manila Speaker Bureau Logistics Planner is main point of contact of Venue, Food & Beverage, and Audio-Visual vendors on behalf of our client’s field force sales reps through the planning logistics of these successful and compliant meetings.  Essential Duties & Responsibilities Collaborate as an integral part of the client Core Team which comprises of meeting planners and speaker bureau planners and other planner roles supporting the logistics of each meeting.Coordinate all aspects of the planning and delivery of relevant meeting logistics in a timely manner within the client’s business rules and budgetary requirement.Confirm and secure location/venue booking of each meeting assigned, applying venue compliance following business rules and approved SOP of each client team.Plan and confirm Food & Beverage needs of the meeting for the Sales Rep, Speaker and all attendees considering any requested special F&B needs of the meeting.Review and secure all audio-visual needs for the meeting including specific requests or needs by the Sales Rep or the Speaker(s) of the meeting.Coordinate venue, food/beverage, and AV confirmation with Meeting Planner through standard documentation and communication within the meeting lifecycle.Ensure all related tasks, required documents are sent and confirmed in a timely manner as measured by task due dates and applicable service level deliverables.Communicate timely with meeting planner, speaker bureau planner and vendors related to task completion and other related inquiry or follow up needs.Application of client business and compliance rules throughout the planning process, especially related to venue appropriateness and negotiated rates within compliance rules.Ability to trigger or escalate any items that can impact risk on meeting compliance.Complete work within client defined SLA parametersEnsure understanding of system functionalities related to job function as assigned.Liaise with relevant internal and external stakeholders to ensure appropriate team members have the most up to date information.Comply with timekeeping standards & policies in Sprout, PSA ensuring accurate work hours are logged.Other related team task maybe assigned.Qualifications 2+ years of (events) planning, and/or customer service experience or equivalentPrevious work experience in catering to US clients, preferably in a phone-based Customer Service role, is requiredRelevant events or meeting planning experience is preferredPharma Industry experience is a plusFamiliarity with US cultural norms and practices to better understand and service stakeholders and clients.Bachelor's Degree Required.Proficiency in PC applications, Microsoft Office suite of products (Word, Excel, PowerPoint, Teams) and Outlook is required.Knowledge in SharePoint, Salesforce and Smartsheet preferred.Proficiency in using phone systems such as Twilio, CRM software and other relevant technology is preferredAbility to carry out analysis and information gathering to resolve problems on routine matters.Able to work during US standard business hours and be flexible on work schedule and/or extended hours to meet clients’ business needs during peak season.Ability to multi-task/plan numerous meetings simultaneously while still demonstrating a strong attention to detail.Able to be flexible to report onsite frequently, dependent on business needConducive work space when working remotely at home, which includes ability to receive and make calls during your shift, work with company provided dual monitors and have appropriate internet speed is requiredComfortable working in a fast-paced team environment, while also able to work independently.Exceptional customer service skillsA strong sense of urgency and the ability to effectively problem solve.Excellent oral and written communication skills with focus on the ability to be concise and clear, summarize a situation and articulate the necessary next steps, effectively listen, and assess the need for urgent action.Collaborate as an integral part of the project team to execute world class events as measured by internal and external client satisfactionIQVIA 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 Description Responsible for providing support to clients of Compliance Services, specifically for Transparency. This role is versatile but is focused on transparency reporting which requires a higher level of technical proficiency and familiarity with data and data manipulation concepts. Familiarity with Pharmaceutical compliance regulations is helpful. Detailed process orientation and superior communication skills is critical. Responsibilities • Perform Transparency Reporting tasks including: - Data validation – validating data against other sources  - Data remediation – updating data based on provided business rules  - Data Analytics – looking for trends in data, and provided related reporting - Transparency Reporting – generate draft reports, understand methods for reporting, be able to articulate methods • Sends information requests to clients for required information. (e.g., missing information, clarification of information, documentation) • Track activities, and report activity data to client. • Perform quality reviews and validation of data inputs • Adherence to various policies (i.e. confidentiality, sensitive communication, intellectual property) • Provide weekly reports on status of all activities to Client stakeholders  • Reporting automation activities using BI tools Competency Requirements • Background in Pharmaceutical, Technology Services or Software Industry desirable, but not mandatory • Proficiency in MS-Office, Word, and Outlook • Advanced abilities with MS Excel required to do data analysis and validation – Power Query and VBA Macros • Knowledge with Power BI or other BI tools • Good organizational skills and ability to meet deadlines working within a time sensitive environment • Ability to multi-task and prioritize • Superior customer service • Excellent communication and interpersonal skills, with the ability to build strong relationships internally and work within a team environment Education, Skills, Experience Desired • Bachelor’s degree or equivalent • 3 years related work 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.

Job Description Responsible for providing support to clients of Compliance Services, specifically for Transparency. This role is versatile but is focused on transparency reporting which requires a higher level of technical proficiency and familiarity with data and data manipulation concepts. Familiarity with Pharmaceutical compliance regulations is helpful. Detailed process orientation and superior communication skills is critical. Responsibilities • Perform Transparency Reporting tasks including: - Data validation – validating data against other sources  - Data remediation – updating data based on provided business rules  - Data Analytics – looking for trends in data, and provided related reporting - Transparency Reporting – generate draft reports, understand methods for reporting, be able to articulate methods • Sends information requests to clients for required information. (e.g., missing information, clarification of information, documentation) • Track activities, and report activity data to client. • Perform quality reviews and validation of data inputs • Adherence to various policies (i.e. confidentiality, sensitive communication, intellectual property) • Provide weekly reports on status of all activities to Client stakeholders  • Reporting automation activities using BI tools Competency Requirements • Background in Pharmaceutical, Technology Services or Software Industry desirable, but not mandatory • Proficiency in MS-Office, Word, and Outlook • Advanced abilities with MS Excel required to do data analysis and validation – Power Query and VBA Macros • Knowledge with Power BI or other BI tools • Good organizational skills and ability to meet deadlines working within a time sensitive environment • Ability to multi-task and prioritize • At least 1 year senior level reporting analyst • Excellent communication and interpersonal skills, with the ability to build strong relationships internally and work within a team environment Education, Skills, Experience Desired • Bachelor’s degree or equivalent • 5 years related work 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.

We are looking for a motivated and customer-focused IT Support Specialist to join our growing team in Bulgaria. In this role, you will provide second-tier remote IT support to end users, ensuring timely service restoration and effective problem resolution. You will work with a wide range of technologies while collaborating closely with Service Desk and IT Operations teams to deliver an excellent user experience. This is an opportunity to deepen your technical expertise, contribute to continuous improvement initiatives, and support a dynamic, international environment. As an IT Support Specialist, you will: Diagnose, recreate, and resolve user issues related to operating systems, applications, and network environments.Identify root causes of recurring problems and recommend system modifications to reduce future incidents.Escalate complex or high-impact issues to senior teams or management, providing clear documentation and status updates.Ensure compliance with established IT policies, procedures, and security standards.Propose creative, effective solutions to improve efficiency, productivity, and end-user satisfaction.Deliver end-user training and guidance when needed.Support and mentor less experienced Service Desk colleagues, sharing best practices in problem resolution and communication.Maintain strong working knowledge of the IT operating environment, tools, client applications, and Service Desk processes.Collaborate with IT Operations to ensure smooth service delivery across systems and applications.Perform additional duties as required to support business needs.Participate in occasional after-hours support, managed in compliance with Bulgarian labor legislation.Required Qualifications & Experience Bachelor’s degree in Computer Science, Information Technology, or a related field.Hands-on experience supporting PC software in a networked environment (Microsoft operating systems, Office applications, email systems, etc.), or an equivalent combination of education and experience.Working knowledge of Microsoft server, workstation, and networking technologies (intermediate level).Understanding of industry standards and best practices for system and network administration.Strong verbal and written communication skills, with the ability to explain technical concepts to non-technical users.Nice to Have Experience working in a shared services or international environment.Familiarity with ITSM tools and incident/problem/change management processes.A proactive mindset and passion for improving user experience.Why Join UsWork in a collaborative, international IT environment.Develop your technical and professional skills through exposure to diverse systems and challenges.Be part of a team that values knowledge sharing, continuous improvement, and innovation.Competitive compensation and benefits aligned with the Bulgarian market.Stable role with opportunities for growth within IT Operations or specialized technical paths.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 monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions• 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.• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications • Native Bulgarian language and English proficiency• Bachelor's Degree Degree in scientific discipline or health care preferred. Req• Requires at least 1 year of on-site monitoring experience. Req• Equivalent combination of education, training and experience may be accepted in lieu of degree. Req• 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).• Good therapeutic and protocol knowledge as provided in company training.• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).• Written and verbal communication skills including good command of English language.• Organizational and problem-solving skills.• Effective time and financial management skills.• Ability to establish and maintain effective working relationships with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Responsibilities: 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.  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. Job Requirements: Bachelors Degree in Pharmaceutical or related field Min. 1 - 3 years of experience in clinical research environment Open to candidates from non-clinical research environment but strong experience in administrative duties Basic knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Broad knowledge of applicable protocol requirements as provided in company training Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint Good 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 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 Standard Operating Procedures (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.• Read and acknowledge all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion and documented. Work towards ensuring your individual training plan and training transcript are reconcilable.• 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.• Liaise with different functional team members, e.g. project management, clinical, data management• health care professionals e.g. investigators, medical monitors, site coordinators and designees to address project related issues.• May liaise with client in relation to details on day to day case processing activities.• 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.• Perform other duties as assigned.• Lead/ Support department Initiatives• 100% compliance towards all people practices and processes• In addition to the above mentioned responsibilities, depending on the project requirement, the team member may perform medical review of non-serious adverse events (AEs) and non-serious adverse drug reactions (ADRs) which includes reviewal of AE coding, past medical history, concomitant medications, expectedness/ listedness, causality assessment and other medical information and ensure completeness and accuracy of data according to applicable regulations and guidelines, SOPs, project-specific guidelines, and medical evaluation guidelines and communicate with the team leads for any correction required in the case and maintain appropriate documentation for all communications. Qualifications• High School Diploma or equivalent Scientific or healthcare discipline or allied life sciences Req• Bachelor's degree in life sciences or related field and up to 3 years of relevant experience, inclusive of up to 1 year of Pharmacovigilance experience. Req• or equivalent combination of education, training and experience. Pref• Good knowledge of medical terminology. Intermediate• Working knowledge of applicable Safety Database and any other internal/Client applications. Intermediate• Knowledge of applicable global, regional, local clinical research regulatory requirements. Intermediate• Excellent attention to detail and accuracy. Intermediate• maintain high quality standards. Intermediate• Good working knowledge of Microsoft Office and web-based applications. Intermediate• Strong organizational skills and time management skills. Intermediate• 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, meet strict deadlines, manage competing priorities and changing demands. Intermediate• Ability to delegate to less experienced team members. Intermediate• Ability to be flexible and receptive to changing process demands. Intermediate• Willingness and aptitude to learn new skills across Safety service lines. Intermediate• Ability to establish and maintain effective communication and working relationships with coworkers, managers and clients. Intermediate• Ability to work as a Team Player, contribute and work towards achieving Team goals. Intermediate• Ensure quality of deliverables according to the agreed terms. Intermediate• Demonstration of IQVIA core values while doing daily tasks Advanced• Extensive use of telephone and face-to-face communication requiring accurate perception of speech. Intermediate• Regular sitting for extended periods of time. Intermediate• May require occasional travel. Intermediate• Flexibility to operate in shifts. Intermediate 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 high quality, on-time input to market research projects in the healthcare field, with limited support and increasing independence in managing project components.• Assignments range in complexity from basic analysis and problem solving to leading components of more complex solutions and contributing to overall project direction. Essential Functions• Lead overall execution of market research project to ensure timely delivery and the development of proposals• Contribute to drafting research materials and other tasks leading up to final report preparation (qualification for either quantitative and qualitative studies as below requirements are acceptable): Quantitative studies: Questionnaire design, table specs, code frames, report charting with error-free, developing key insights and takeaway messages, etc.Qualitative studies: drafting discussion guide, conduct in-depth interviews independently or with limited supervision, prepare content analysis/ summary of IDIs, contribute to qualitative report synthesis, etc.• Proactively develops a market research methodology/industry knowledge through the delivery of market research engagements and participation in formal and informal learning opportunities, and applies this knowledge to improve project outcomes• Well time/resource management when handling multi-studies, with accountability for project deliverables• Keep effective performance & well EQ management under pressure. Qualifications• 1 year and 3 months contract• 6+ years of experience in Market Research (preferred Healthcare & Pharma exp.) (Position level will be aligned with the candidate’s experience.)• Experience in marketing/Product Manager roles in Pharmaceutical companies is also preferred• Mainly act as a project delivery lead, with experience in managing project modules or client communication preferred [추천 컨텐츠]1. What does it mean to be IQVIAN? (video)2. 아이큐비아ㅣ나만 몰랐던 (진짜) 포브스 선정 '세계 최고의 직장' (video)3. [아이큐비아 직업탐구] 정확한 제약시장 분석을 위한 Primary Intelligence (article) [관련 문의]한국 아이큐비아 채용(IQVIA) 카카오톡 채널을 통해 1:1 문의 하실 수 있습니다.*채널을 추가하시면 매월 신규 포지션 알림 및 회사 소식을 받아보실 수 있습니다. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Title: Registered Dietitian – Clinical Research Support Location: Remote (South Korea) Job Type: Freelance / Part-time (ad hoc hours) Are you ready to make a real impact? Do you want to work flexibly from anywhere in South Korea, while advancing your career with a global leader in healthcare innovation? Join IQVIA and become part of a collaborative, forward-thinking team that values your expertise and supports your professional growth. IQVIA is seeking experienced and registered Dietitians to join our team for an international clinical research projects in the field of metabolic disease area. You will support patients participating in clinical studies, provide nutritional and lifestyle guidance, and contribute to improving healthcare outcomes. Key Responsibilities Conduct comprehensive nutritional assessments Provide ongoing counseling and motivational support to study participants Monitor participant progress and outcomes throughout the study period Conduct all meetings and consultations with participants online (telehealth) Collaborate with the clinical research team to ensure adherence to study protocols Maintain accurate and confidential documentation in compliance with regulatory standards Participate in virtual team meetings and training sessions Requirements Certified and Registered Dietitian Fluent in Korean and English; additional language skills are a plus; Strong interpersonal and communication skills Ability to work independently and in a structured manner; clinical experience preferred Proficient with digital tools and telehealth platforms What We Offer Opportunity to contribute to a high-impact international clinical study Remote work and collaboration with an international team All participant interactions and monitoring are conducted online Professional development and exposure to global research standards Why IQVIA? At IQVIA, you’ll be part of a collaborative and forward-thinking team that’s shaping the future of healthcare. We offer a supportive environment, meaningful work, and the chance to grow your career in clinical research. #LI-DNP #LI-CES #LI-HCPN #LI-XS 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.

Estamos em busca de um(a) profissional júnior para atuar na área de Produção OKAI, com foco em contato com painéis e coleta de dados. Essa posição é ideal para quem gosta de rotina estruturada, comunicação e organização.Principais responsabilidades:Realizar contato ativo com farmácias utilizando abordagem e roteiro definidos Incentivar a participação das farmácias em painéis contínuos Executar follow-ups para garantir a taxa de retorno dos participantes Atender chamadas recebidas, esclarecendo dúvidas simples e direcionando casos mais complexos Apoiar o envio de materiais físicos de coleta de dados Coletar e registrar informações assegurando a qualidade dos dados Requisitos:Ensino médio completo Boa comunicação verbal e escrita Capacidade de seguir processos e instruções Organização e atenção a detalhes Diferenciais:Espanhol básico Experiência prévia com atendimento, call center ou área da saúde 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! 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:The Customer Service – Client Support Specialist plays a key role in supporting our Sales Team and ensuring exceptional service for our Enterprise client accounts. You will collaborate closely with Account Managers and Business Development Directors to streamline sales processes, manage customer requests, and ensure clients receive timely, accurate, and high‑quality support. Responsibilities:Client Support & CommunicationServe as a primary point of contact for customer service inquiries related to sales activities, orders, and account needs. Communicate with Life Sciences, Population Health and Academic clients—including Procurement, Data Management, and Project Management teams—to ensure questions are answered, and issues are resolved quickly and professionally. Support client relationship activities such as sharing updates, resources, upcoming events, and IQVIA Quality Metric initiatives. Sales Process & Administrative SupportPartner with Sales team members to ensure smooth, efficient progression from initial quote to signed sales order. Coordinate with internal proposal and pricing teams to assist with creation, review, and processing of Sales Orders and Change Orders. CRM & Pipeline CoordinationMaintain and update CRM entries, ensuring opportunities, client notes, and follow‑up actions are correctly logged and current. Work with Sales Leadership to support pipeline accuracy, opportunity progression, and follow‑up communications. Leverage client insights and interactions to help identify new opportunities or areas of client need. Minimum Required Education & Experience: Experience in customer service, client support, sales operations, sales coordination, or project coordination—preferably in SaaS or Life Sciences. A bachelor’s degree is highly preferred. Experience supporting sales processes or working within fast‑paced commercial teams. English fluency (this is part of a global area) Proactive problem‑solver person with clear, professional and assertive communication Highly organized & detail‑oriented Experience with Microsoft Navision/365 Business Central, CRM tools, and strong Word and Excel skills preferred. *Resumé/CV must be submitted in English* #home-based IQVIA is committed to embracing a diverse and inclusive work environment. Our goal is to attract and retain the best people, regardless of their gender, race, marital status, ethnic origin, national origin, age, disability, sexual orientation, gender identity or any other characteristic. Join us! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Location: Brazil (Sao Paulo) About Us: Join our team and help shape the future of our organization. We are a leading company committed to excellence and innovation, seeking a talented Senior Recruiter to support our growth. Job Overview: Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements. Key Responsibilities: • Complete appropriate therapeutic, protocol and clinical research training to perform job duties. • Gain experience in study procedures by working with experienced clinical staff. • Under close supervision, perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with contracted scope of work and good clinical practices. • Under close supervision, administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues. • Under close supervision, 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. • Under close supervision, 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 Good Clinical Practice (GCP) /  International Conference on Harmonization (ICH) and local regulatory requirements. • Under close supervision may support start-up phase. • Under close supervision, 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, learn key facets for successful development of project subject recruitment plan on a per site basis. Suggest ideas for improving site recruitment plan in line with project needs to enhance predictability. Assist in tracking subject site recruitment progress. Basic Qualifications: • Bachelor's Degree Degree in scientific discipline or health care preferred. • Equivalent combination of education, training and experience may be accepted in lieu of degree. • Prior clinical experience preferred. • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). • Written and verbal communication skills including good command of English language. • Strong attention to detail and excellent communication skills. • Exceptional problem-solving, judgment, and decision-making abilities. • Organizational and problem-solving skills. • Ability to establish and maintain effective working relationships with coworkers, managers and clients. • Advanced knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. • Knowledge of applicable protocol requirements as provided in company training. Why Join Us? • Be part of an innovative and forward-thinking company that collaborates to make a healthier world. • Work alongside a diverse and talented team. • Many opportunities for professional growth by developing project mgmt abilities. • Competitive salary 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.

Are you passionate about improving patient access to innovative therapies? Join our team as a Business Access Manager in Northern Italy, where you'll play a key role in expanding access to cutting-edge biosimilar medicines in Central Italy (Lazio, Bruzzo, Molise). This is an exciting opportunity to work with a leading biopharmaceutical company that is dedicated to bringing high-quality biologics to market at cost-effective prices. Job Overview:  In this role, you will manage commercial activities and engage with hospital stakeholders to promote a range of specialist biosimilar products. You will collaborate with colleagues to provide decision-makers with the necessary information for optimal adoption and prescribing. Your responsibilities include establishing our client as a trusted partner in the biosimilars/biologics market, collecting and reporting relevant data, and achieving sales and market share growth. Qualifications : Pharmaceutical sales experience within hospitals, especially with high-cost drug pharmacists within hospitals. Experience in biosimilars or therapy areas such as Rare Disease, Haematology, Nephrology, Ophthalmology, Immunology, Oncology, Endocrinology, Orthopaedics, or Rheumatology. Life Sciences degree or equivalent; advanced degrees in Business Administration or Health Economics are a plus. Strong relationship-building skills with both external and internal customers. Fluent in Italian and English. Willingness to travel regularly throughout the territory. Full driving license essential. #LI-CES  #LI-CS1 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is 52 600,00 € - 78 800,00 €. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA is seeking an International Project Support Coordinator, to provide administrative support to the field based staff of complex multiple projects, and helping with the smooth running of day to day activities for the team. This will be a varied and busy role, where strong administrative experience, excellent communication skills and ability to work autonomously are essential.  The successful candidate will be an effective communicator with an excellent telephone manner, ideally with experience of working within a support / call centre role who can demonstrate strong IT/data skills, strong time management skills and is proficient with MS Office packages and ideally CRM knowledge. Responsibilities To work collaboratively across the Team Coordinator function, and understand how the function contributes to the Commercial business. To be the first point of contact for all queries relating to the project, handling and addressing issues where appropriate, or else directing queries to the most appropriate contact. To follow processes and procedures (new employee, leaver, transfer) and work with departments (HR, Fleet, Resourcing, HR-PSC, Amex, BT etc.) to ensure effective team administration. Ensure that systems are updated accordingly. To track levels of absence, identify sickness trends within the project and highlight cost implications as appropriate. To facilitate production and documentation of presentations and organize team/customer meetings, finalizing minutes in collaboration with Project Director To support Month end administration, ensuring daily rates are allocated to field teams along with relevant time sheet, accurately collate information in connection with the Rolling Forecast, within project deadlines. To conduct financial tracking for project revenue recognition and liaising with Management Accounts. To undertake diary management of Project Director. Skills and Qualifications Good verbal and written communication skills, telephone manner, team working skills, flexible attitude to work Good prioritization skills Fluency in English and Spanish Able to use initiative, plan ahead, proactive in problem solving, diplomatic and able to demonstrate appropriate decisions within scope of authority Able to share experience and learning, able to priorities and liaise with field staff and customers effectively Intermediate understanding of Word, Power point and basic Excel Ability to establish and maintain effective working relationships with co-workers, managers and clients. Eligibility to work full-time in the EU #LI-CES #LI-CS1 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.

Job Title: Registered Dietitian – Clinical Research Support Location: Remote (France) Job Type: Freelance / Part-time (ad hoc hours) Are you ready to make a real impact? Do you want to work flexibly from anywhere in France, while advancing your career with a global leader in healthcare innovation? Join IQVIA and become part of a collaborative, forward-thinking team that values your expertise and supports your professional growth. IQVIA is seeking experienced and registered Dietitians to join our team for an international clinical research projects in the field of metabolic disease area. You will support patients participating in clinical studies, provide nutritional and lifestyle guidance, and contribute to improving healthcare outcomes. Key Responsibilities Conduct comprehensive nutritional assessments Provide ongoing counseling and motivational support to study participants Monitor participant progress and outcomes throughout the study period Conduct all meetings and consultations with participants online (telehealth) Collaborate with the clinical research team to ensure adherence to study protocols Maintain accurate and confidential documentation in compliance with regulatory standards Participate in virtual team meetings and training sessions Requirements Certified and Registered Dietitian Fluent in French and English; additional language skills are a plus Strong interpersonal and communication skills Ability to work independently and in a structured manner; clinical experience preferred Proficient with digital tools and telehealth platforms What We Offer Opportunity to contribute to a high-impact international clinical study Remote work and collaboration with an international team All participant interactions and monitoring are conducted online Professional development and exposure to global research standards Why IQVIA? At IQVIA, you’ll be part of a collaborative and forward-thinking team that’s shaping the future of healthcare. We offer a supportive environment, meaningful work, and the chance to grow your career in clinical research. #LI-DNP #LI-CES #LI-HCPN #LI-XS 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 monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions• 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.• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications• Bachelor's Degree Degree in scientific discipline or health care preferred. Req• Requires at least 1 year of on-site monitoring experience. Req• Equivalent combination of education, training and experience may be accepted in lieu of degree. Req• 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).• Good therapeutic and protocol knowledge as provided in company training.• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).• Written and verbal communication skills including good command of English language.• Organizational and problem-solving skills.• Effective time and financial management skills.• Ability to establish and maintain effective working relationships with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Créée en 2010, l’agence RCA Factory accompagne les acteurs de la santé dans la définition et la mise en œuvre de leur stratégie de communication social media et de marketing digital. RCA Factory propose une large gamme de services permettant aux entreprises, aux organisations et aux dirigeants de communiquer auprès de leurs publics sur les réseaux sociaux. RCA Factory est aussi experte dans la création et l’animation de communautés de patients ou de professionnels de santé.  L’agence a d’ailleurs elle-même fondé 2 médias 100% digital/social media : We are Patients, le média des patients engagés et de leurs proches, suivi par plus de 250 000 personnes et Buzz Comptoir le média de l’équipe officinale. RCA Factory est enfin à l’initiative d’Influence For Health, l’événement phare des créateurs de contenus en santé.   RCA Factory emploie 30 collaborateurs et compte parmi ses principaux clients : Sanofi, Servier, Boehringer Ingelheim, Pierre Fabre, GSK, Merck, le Groupe Elsan, La Médicale, UCB, CRIP Pharma, GIE GERS, l’AF3M...    RCA Factory fait partie du groupe IQVIA depuis septembre 2025.    Rôle  RCA Factory recherche un(e) Responsable du pôle créatif pour structurer, animer et faire évoluer son équipe de création multimédia dans un environnement santé exigeant.  Le poste combine direction créative, production opérationnelle, management d’équipe et intégration concrète de l’IA dans les méthodes de travail.  L’objectif : faire émerger un véritable lab créatif IA, capable d’accélérer l’idéation, d’améliorer la qualité des livrables, de renforcer les réponses aux appels d’offres et d’imaginer de nouveaux formats créatifs.        Missions  1) Développer l’usage de l’IA dans la création  Vous mettez en place une démarche IA concrète et utile : veille, tests, prototypes, workflows, bonnes pratiques et cas d’usage.  Vous identifiez les usages les plus pertinents pour l’idéation, les concepts, la direction artistique, l’image, la vidéo, le motion design, les réseaux sociaux, les présentations et la production de contenus.  Vous accompagnez les équipes dans l’adoption des outils IA, avec un cadre clair intégrant qualité, éthique, conformité, confidentialité et contraintes santé/pharma.  2) Piloter le pôle créatif  Vous managez une équipe composée de profils créatifs, vidéo, motion design, design et freelances.  Vous organisez les ressources, priorisez les sujets, fluidifiez les échanges avec les équipes conseil et projet, et garantissez le respect des délais.  Vous êtes garant(e) de la cohérence créative, de la qualité d’exécution, de la clarté des messages et de l’impact des livrables.  3) Contribuer aux appels d’offres et recommandations  Vous participez aux réponses aux appels d’offres : analyse des briefs, angles créatifs, concepts, storytelling, moodboards, prototypes, maquettes et présentations.  Vous apportez une vision créative différenciante, structurée et réaliste, capable de convaincre tout en restant opérationnelle.  Vous utilisez l’IA comme levier d’exploration, de visualisation rapide et d’accélération des recommandations.  4) Produire et superviser les projets créatifs  Vous intervenez sur des projets créatifs variés : territoires de marque, directions artistiques, contenus social media et digitaux, présentations, design, motion design et vidéo.  Vous êtes capable de produire directement lorsque nécessaire : maquettes, prompts, images de référence, storyboards, scripts, assets, présentations ou adaptations.  Vous supervisez la production de bout en bout : cadrage, planning, validation, itérations, contrôle qualité et livraison.  Le profil recherché  Vous justifiez d’une expérience confirmée en direction créative digitale, direction artistique ou pilotage de pôle créatif.  Vous possédez une solide culture social media, digitale, vidéo, motion design, design, contenus de marque et présentations stratégiques.  Vous êtes à la fois stratégique et opérationnel(le), capable de définir une vision tout en produisant, prototypant et prenant des décisions rapidement.  Vous avez déjà managé des équipes créatives, coordonné des freelances et accompagné la montée en compétences de profils créatifs.  Une expérience dans la santé, la pharmacie ou un environnement réglementé constitue un véritable atout.  Compétences IA attendues  Vous maîtrisez les principaux usages de l’IA générative appliqués à la création : idéation, benchmark, moodboards, concepting, rédaction, image, vidéo, motion design, présentation et automatisation.  Vous savez construire des prompts précis, itérer, documenter vos méthodes et contrôler la qualité des résultats.  Vous êtes capable d’intégrer l’IA dans des workflows hybrides combinant outils créatifs traditionnels, génération IA, retouche, montage, design, validation humaine et conformité.  Vous connaissez les limites et les risques liés à l’IA : droits d’usage, confidentialité, données sensibles, biais, hallucinations, traçabilité, validation médicale ou réglementaire et cohérence de marque.  Outils appréciés  Une bonne connaissance des outils suivants est attendue ou fortement appréciée :  ChatGPT, Claude, Gemini ou Perplexity pour l’idéation, la synthèse, la rédaction et la structuration.  Midjourney, DALL·E, Adobe Firefly, Ideogram ou Leonardo AI pour l’exploration visuelle et la direction artistique.  Runway, Kling, Luma, Pika, HeyGen ou Synthesia pour les prototypes vidéo, animatiques, storyboards ou formats courts.  Adobe Creative Cloud, Figma, Canva, Gamma ou Tome pour la production, les maquettes et les présentations.  Notion, Miro, Airtable, Zapier ou Make pour l’organisation, la documentation et les workflows.  Ce que nous attendons  Un équilibre fort entre vision stratégique, exigence créative et capacité d’exécution.  Une approche structurée de la création, pensée comme un système : concept, ton, direction artistique, formats, déclinaisons et production.  Une capacité à faire progresser les équipes, les outils et les méthodes, avec l’IA comme levier d’innovation.  Une attention constante portée à la clarté, à la crédibilité, à l’impact et à la qualité finale.  Pourquoi nous rejoindre  Pour contribuer à des projets à impact dans le secteur de la santé.  Pour jouer un rôle clé dans la structuration et la montée en puissance du pôle créatif.  Pour bénéficier d’une forte autonomie dans le développement d’une culture créative enrichie par l’IA.  Pour travailler sur des projets mêlant stratégie, design, contenu, social media, vidéo, production et nouveaux formats.    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。 【部署・チーム名】 Medical Writing部門では、国内外の製薬会社・ベンチャー企業等から、幅広い治療分野の業務を受託しているため、様々な文書作成に携わり、非常に多くの経験をすることができます。また、社内の教育システムも充実しており、新規案件に対して専門的なアプローチが可能な体制になっています。 【主な業務内容】 リード・メディカル・ライターとして次のような業務をお任せします。・臨床試験関連文書（治験実施計画書、治験総括報告書、コモンテクニカルドキュメント）の作成およびレビュー業務・グローバル試験の治験実施計画書に対して日本要件を満たすための修正版の作成およびレビュー業務・臨床研究・PMS関連文書（実施計画書、安全性定期報告書、論文など）の作成およびレビュー業務・プロジェクトの進捗管理、人員管理、予実管理、顧客対応・後輩スタッフの指導、他 【求める人物像】 【必須要件】 ・Medical Writing経験5年以上（翻訳のみは不可）・理系大学、大学院卒・医薬品開発全般、GCP、ICH関連ガイドラインを理解している・国内の薬事規制に関する知識を有する・薬学･医学・統計学の基礎知識を有する・英語スキル：読み書きができる（英文書Review・添削ができる、英文和訳ができる、英文レポート作成ができる）、目安：TOEIC 730以上、会話は日常会話程度・Fluency in Japanese would be required 【歓迎要件】 ・非臨床（薬理、毒性、ADME）の知識、ご経験がある方 ・臨床薬理の知識、ご経験がある方 【このポジションの魅力・キャリアパス・チーム構成・雰囲気】 ・医薬品、医療機器、再生医療等幅広い分野の開発品目に関する文書作成を経験できます ・文書作成に際し、社内の医師や薬事の専門知識を有する者からアドバイスを受けることできます ・グローバルメディカルライティングのメンバーとしてグローバルな環境で仕事をすることができます 【勤務地】 全国フルリモート可 【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 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 【選考ステップ（オンライン完結）】 ①書類提出（履歴書・職務経歴書）②書類選考③筆記試験&人事面談（オンライン）※計2時間15分④部門面接（オンライン）◆補足◆部門面接について- 部門マネジャー　30分の個別面接- 部門ディレクター　1時間の個別面接同日に1時間30分続けて実施※難しい場合は別日に分けて調整が可能です。 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。 【部署・チーム名】Medical Writing部門では、国内外の製薬会社・ベンチャー企業等から、幅広い治療分野の業務を受託しているため、様々な文書作成に携わり、非常に多くの経験をすることができます。また、社内の教育システムも充実しており、新規案件に対して専門的なアプローチが可能な体制になっています。 【主な業務内容】メディカルライター（担当者）として次のような業務をお任せします。 臨床試験関連文書（治験実施計画書、治験総括報告書、コモンテクニカルドキュメント等）の作成 グローバル試験の治験実施計画書に対して日本要件を満たすための修正版の作成 製造販売後調査関連文書（安全性定期報告、再審査申請資料等）の作成 臨床研究報告書・論文の作成 各種文書のQC　他 【求める人物像】 必須条件 Medical Writing実務経験がある（翻訳のみの方は対象外） 理系大学、大学院卒 薬学･医学的な基礎知識を有する 医薬品開発全般、GCP、ICH関連ガイドライン、国内薬事規制(GPSP等)を理解している 英語の読み書きが可能（辞書を使って英文書の添削や和文英訳が可能なレベル） Fluency in Japanese would be required 歓迎要件 非臨床（薬理、毒性、ADME）の知識、ご経験がある方 臨床薬理の知識、ご経験がある方 【このポジションの魅力・キャリアパス・チーム構成・雰囲気】 医薬品、医療機器、再生医療等幅広い分野の開発品目に関する文書作成を経験できます 文書作成に際し、社内の医師や薬事の専門知識を有する者からアドバイスを受けることできます グローバルメディカルライティングのメンバーとしてグローバルな環境で仕事をすることができます 【勤務地】 全国フルリモート可 【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 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（オンライン完結）】①書類提出（履歴書・職務経歴書） ②書類選考 ③筆記試験&人事面談（オンライン）※計2時間15分 ④部門面接（オンライン） ◆補足◆ 部門面接について - 部門マネジャー　30分の個別面接 - 部門ディレクター　1時間の個別面接 同日に1時間30分続けて実施 ※難しい場合は別日に分けて調整が可能です。 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.

Financial Analyst (13-Month Fixed Term Contract) Location: Sydney, NSW IQVIA is seeking a motivated Financial Analyst to join our team on a 13-month fixed term contract. This role is ideal for recent graduates or early-career professionals looking to build strong foundations in financial planning & analysis (FP&A), reporting, and month-end close processes. Working under close guidance, you will support financial and transactional accounting activities, contributing to budgeting, forecasting, and business planning initiatives. Key Responsibilities Assist in financial analysis to support business and strategic planning, budgeting, and forecasting processesSupport the month-end close process, including journal entries, reconciliations, and reportingAssist with post Accounts Receivable (AR) activities, including tracking and analysisPrepare and maintain regular financial reports and dashboardsProactively maintain financial reporting systems, including data collection and consolidationPerform ad hoc financial analysis and general finance administration as requiredLiaise with operational and finance stakeholders to resolve routine financial queries and discrepanciesSupport audit processes and provide assistance with compliance-related activitiesIdentify opportunities to improve processes and data accuracyProactively manage cash collection though co-ordination between project managers, delivery teams, and clients. Generate monthly AR Aging report and update commentary for regional & corporate reporting.Skills & Experience 1–3 years’ experience in Financial Planning & Analysis (FP&A), accounting, or related finance rolesExposure to month-end close processes is highly desirableExperience with Hyperion and PeopleSoft is strongly preferredStrong proficiency in Microsoft Excel and financial systemsSolid analytical and problem-solving skills with attention to detailAbility to manage multiple priorities and work effectively under pressureStrong interpersonal and communication skills, with the ability to engage stakeholdersQualifications Bachelor’s Degree in Accounting, Finance, or a related discipline (required)What We’re Looking For A proactive and detail-oriented individual eager to develop their finance careerStrong willingness to learn and adapt in a fast-paced environmentAbility to work both independently and collaboratively within a teamConfidence to communicate insights and support decision-makingWhy Join Us? Excellent opportunity to gain hands-on experience in FP&A and corporate financeExposure to leading financial systems and toolsSupportive and collaborative team environmentPathway to longer-term opportunities based on performanceIQVIA 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.

Case ManagerCase Managers serve as subject matter experts responsible for resolving complex patient, provider, pharmacy, and client support issues that fall outside standard program workflows and business rules. This role provides both inbound and outbound phone support for escalated cases identified by Care Managers, clients, leadership, and stakeholders. The Case Manager investigates issues, coordinates cross-functional resolutions, educates stakeholders, and ensures an exceptional service experience through proactive case ownership and timely resolution of complex support requests. This is a remote position.   The information contained herein is intended to be an accurate reflection of the duties and responsibilities of the individuals assigned to this position. They are not intended to be an exhaustive list of the skills and abilities required to do the job. IQVIA reserves the right to revise the job or to require that other or different tasks be performed as assigned. ResponsibilitiesClient Support·Serve as a dedicated resource for clients requiring advanced case support and issue resolution.·Manage referrals involving complex reimbursement, claims, affordability, benefit verification, and patient access concerns.·Provide inbound and outbound communication with clients, healthcare providers, pharmacies, patients, and stakeholders to facilitate resolution.·Partner with clients, and internal operational partners to address high-priority or time-sensitive patient situations.·Deliver white-glove service and proactive follow-up for complex cases requiring enhanced oversight and coordination.Additional Key Responsibilities Handle escalations involving repeat callers, claim disputes, exception requests, client-approved overrides, and situations requiring enhanced case ownership.Review and resolve support requests received through the Escalation Tool, HUB Portal requests, referrals, inbound calls, emails, and internally generated escalations.Maintain ownership of assigned cases through resolution, ensuring all actions, root causes, and outcomes are appropriately documented.Responsible for answering in-bound and making outbound calls and assisting customers with pharmacy-related services.Obtain client information by answering telephone calls; interviewing clients; verifying information.Contact insurance companies for benefit investigation and coverage eligibility.Provide customers with courteous, friendly, fast, and efficient service.Update job knowledge by participating in educational opportunities and training activities.Work efficiently both individually and within a team to accomplish required tasks.Maintain and improve quality results by adhering to standards and guidelines and recommending improved procedures.Any additional duties as assigned by program management.ScheduleMust be available to work an 8-hour shift between 8:00 AM and 8:00 PM ESTRequired Qualifications:High School diploma required or equivalent.Must currently be working on an AbbVie projectDemonstrated time management skills; planning and prioritization skills; ability to multi-task and maintain prioritization of key projects and deadlines.Demonstrated effective presentation skillsExcellent interpersonal (written and verbal) communication skills.Demonstrated effectiveness to work cross-functionally within a team.Demonstrated ability to work effectively in an independent environment.Demonstrated ability to build relationships with customers and third parties.Demonstrated ability to adapt to a fast-paced, changing work environment and responsibilities.Fully competent in MS Office (Word, Excel, PowerPoint)Excellent documentation accuracyDrive and enthusiasm for supporting customers.Excellent listening and problem-solving skillsPrevious data entry experience and ability to type 30wpm+Ability to use MS Office Must reside in country where the job is posted.Preferred Qualifications:Associate degree or higher preferred.Minimum 2+ years’ experience in medical billing, insurance verification, or similar patient services experience preferred.Experience using a CRM and integrated telephony platform a plus.Bilingual (Spanish) highly desirableNote: This role is not eligible for visa sponsorship. Candidates must have authorization to work in the US without the need for sponsorship.  #LI-CES #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is 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 $54000 to $56700 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.