IQVIA

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

Job Overview Engage with Client CEOs and Senior Management to generate awareness about IQVIA, sell consulting engagements and continuously reinforce IQVIA position with this stake-holder group.Principal will typically carry an individual target and will also carry additional bid-team targets, and will work under the supervision of Country Principal to develop a business development plan and pursue it.Expected to deliver the targeted profitability for the “book” managed, pricing the proposals right and ensuring on-time, on-cost deliveryPrincipal Life Sciences will be expected to have significant knowledge in Pharma/LifeSciences Strategy projects and be well known in the industryPrincipal will actively oversee the engagements sold by them and/or other engagements being run, and ensure high quality delivery, leading to good client satisfaction scoresPrincipal is expected to contribute to the enhanced awareness of IQVIA Consulting in the market place, e.g. through speaking engagements, client meetings, publications etc. Expected to proactively continue to strengthen subject matter expertise through on the job experience, participation in conferences and symposiums and other forums for professional knowledge sharing.Expected to proactively mentor, coach and share subject matter expertise with others to elevate our capabilities to deliver world-class solutions for clients.May have responsibility for managing one or more Engagement Managers and the team below. Minimum Education, Experience, & Specialized Knowledge Required: MBA from premier school with at least 15+ years’ experience in the consulting industry & pharma (Strategy).In depth and long-standing relationships with client companies, especially at a senior level. Requires deep expertise in at least one practice along with knowledge of all other practices.Possesses exemplary business development skills.Consulting experience is a mustDesired Experience From Consulting organizations leading LifeSciences/Pharma Strategy projects. Mix of BD, Delivery & good network in the Pharma Industry.Additional Requirements: Has broad knowledge of the pharmaceutical industry.Works willingly and effectively with others in and across the organization to accomplish team goals.Knowledge and understanding of the fundamental processes of business, their interaction and the impact of external/internal influences on decision making, growth and decline.Knowledge of consulting methods, tools and techniques, related to functional area. Knowledge and understanding of the marketplace and professional/trade associations key people and companies.Demonstrated strategic thinking and planning and change management skills.Excellent interpersonal and networking skills.Values people’s opinions and encourages knowledge sharing.High level of energy, drive and enthusiasm.Able to manage complex relationships and juggle priorities.Ability to profitably price engagements. Has excellent client relationship and influencing skills.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Position Title: Mass Market Representative Location: MozambiqueIndustry: FMCG / HealthcareEmployment Type: ContractorFluency In English Essential A leading Consumer Healthcare company is seeking a results-driven Mass Market Representative with proven experience in the FMCG or retail pharmacy space. This role is ideal for a candidate with strong field execution skills, a passion for consumer health, and the ability to drive visibility and availability of products across mass market channels. Key Responsibilities: Visit channel-specific outlets regularly to ensure product availability in collaboration with distributor teams.Deploy company Point-of-Sale Materials (POSM) across assigned outlets.Oversee and support the execution of company activations within the designated channel.Submit weekly, monthly, and quarterly reports on sales, stock levels, and market activities.Gather and report market insights and competitor activities to inform strategy.Qualifications & Requirements: Minimum of a diploma in Sales, Marketing, or a related field; a degree is an advantage.At least 3 years’ experience in the FMCG environment.Fluency in English required for the recruitment process and recruitment documentationPrevious experience working in retail pharmacy is beneficial.Valid driver’s license and access to a reliable vehicle.Must be a resident of the country in scope and legally able to work there.Why Join Us?This is a great opportunity to be part of a dynamic team focused on delivering impactful consumer healthcare solutions. You’ll play a key role in driving brand visibility, market execution, and retail excellence. #LI-DNP #LI-CES  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com 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 IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to manage Early Phase clinical research projects in different therapeutic areas and to cooperate closely with one of our key clients. We currently offer the exciting opportunity to join the team as Clinical Trial Manager in full-time and work home-based in Italy. In this role you will be accountable for the operational and scientific oversight, the set-up, execution and delivery of your assigned clinical trials at the regional/local level. working closely together with the Clinical Trial Lead, the CRAs and the regulatory start-up team in the assigned trial. KEY RESPONSIBILITIES • Accountable for the operational and scientific oversight, the set-up, execution and delivery of their assigned clinical trials at the regional/local level. CTMs contribute to delivery of sponsor´s pipeline through accurate planning and efficient execution of trials that bring speed & value to participating patients and sites• Provides leadership and direction to the Operational Unit trial team and is accountable for the overall success and delivery of their assigned clinical trial/s according to defined milestones and key performance indicators • Responsible for steering and directing clinical trial activities, including patient and site engagement activities and interaction with multiple internal and external stakeholders and trial team members at a regional/local and global level • Responsible for managing the planning, implementation and tracking of the clinical trial process as well as risk mitigation. The CTM serves as a proactive member of the trial team, liaising closely with the Clinical Trial Leader (“CTL”) on all study-related issues Trial Preparation, Conduct and Closeout:• Accountable for the trial activities for responsible R/OPU• Verify the trial is conducted in compliance with GCP-ICH, local/global regulations, application SOPs and according to the trial protocol by overseeing CRO and internal team activities • Creation, management, and review of the R/OPU trial budget to verify appropriate level of financial oversight and planning accuracy• Appropriate trial-specific training of R/OPU internal and external partners.• Accurate planning and co-ordination of operational feasibility of trial timelines for their R/OPU; and oversight of trial preparation to verify trial team members are aligned and on track • Verifies and provides input into the country and site level feasibility and OPU commitment • Development and implementation of country level engagement plans, recruitment planning and risk mitigation • Oversees outsourcing of vendor services in the R/OPU in accordance to operating models and governance • Verify timely responses to questions from Regulatory Authority/Ethic Committee and other external stakeholders• Maintains oversights during clinical trial conduct including adherence to GCP and all global and local regulatory requirements; verifies budget oversight, including support of regular clinical quality monitoring, and safety reporting • Support CTL during investigator meetings• Responsible for timely, complete, and compliant archiving of all relevant R/OPU documents in the TMF, including all required documents from vendors • Verifies timely submission of the CTR to Regulatory authority/Ethics Committee and other external stakeholders as required by local regulations • Shares information on trial results with Investigational sites and, if applicable, patients Leadership competencies • Create an environment that inspires, motivates, and empowers colleagues, contributing to acceleration of clinical development timelines and value creation for patients• Embraces innovative approaches and technologies, as well as creates and maintains a culture that drives empowerment and smart risk taking REQUIRED KNOWLEDGE, SKILLS AND EXPERIENCEEducation & Background• Master’s degree or higher in Life Sciences preferred• Extensive experience in clinical research, including a minimum of 3 year in clinical trial management• Mandatory prior involvement in clinical trials conducted in Italy• Experience with Early Phase clinical trials (Phase I and Proof-of-Concept) is an advantageRegulatory & Quality Expertise• Expert knowledge of applicable clinical research regulations, including GCP and ICH guidelines• Strong attention to detail, accuracy, and a results-oriented, quality-driven approachProject, Financial & Vendor Management• Strong understanding of project financials, including contractual obligations and financial implications• Proven experience in vendor selection, oversight, and effective vendor management• Ability to organize resources, plan activities in advance, and adapt to changing circumstancesTherapeutic Area knowledge• Previous experience in OncologyLeadership & Decision-Making• Demonstrated leadership capability to deliver results through others, ensuring quality, timelines, and performance management, including feedback• Ability to make sound decisions by synthesizing complex and disparate information• Experience influencing business partners within matrix and cross-functional environments  Organizational & Problem-Solving Skills• Excellent organizational, planning, time-management, and prioritization skills, with the ability to manage multiple projects and conflicting priorities• Strong analytical and problem-solving skills, with a strategic, solution-oriented mindsetCommunication & Collaboration• Excellent written and verbal communication skills• Fluency in Italian language (minimum C1 level) and very good command of English• Strong collaboration and customer service skills• Proven ability to work across geographies with cultural awareness and sensitivityIT & Practical Requirements• Very good computer and software skills, including Microsoft Word, Excel, and PowerPoint• Location: Lombardy Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is 41 000,00 € - 79 800,00 €. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job OverviewAs a Clinical Data Management Lead you will independently manage the delivery of data management services for single/multi-service projects ensuring quality deliverables are provided on time and within budget. You will provide leadership and vision to the Clinical Data Management (CDM) team ensuring high-quality data management products that meet customer needs. Your role will involve project planning execution close-out financial management and communications while complying with Good Clinical Practices (GCPs) and regulatory guidelines. Essential Functions Key responsibilities related to Client Management, Service Management, Financial Management and Business Development Support. Serve as the primary point of contact for customers on data management deliverables. Manage multiple large studies or programs providing leadership and support to Data Team Leads (DTLs). Ensure open communication with customers and IQVIA management to meet contractual obligations. Independently manage DM service delivery ensuring quality and compliance with agreed specifications. Implement proactive quality management plans and drive service improvements. Manage financial aspects of projects including budgets and change orders. Support business development activities including RFP processes and pricing discussions. Lead process improvements and contribute to the development of new technologies or tools. Qualifications Bachelor's Degree in Health Clinical Biological or Mathematical Sciences or related field. 5+ years of direct Data Management experience with 3+ years as a Clinical Data Manager Project Lead. Advance English level and communication skills in the language. Based in Mexico, home based position. Proven competence in managing delivery of multiple global trials through the full Data Managemenr life-cycle. Expert data management skills and advanced knowledge of the processes. Experience in handling complex customer negotiations and bid defense meetings. Knowledge of Medical Terminology Pharmacology Anatomy and Physiology. Excellent communication interpersonal and project management skills. Ability to work independently and establish effective working relationships. 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.

Únete a nosotros en nuestro emocionante trayecto! IQVIA ™ es The Human Data Science Company ™, enfocada en el uso de datos y ciencia para ayudar a los clientes de la salud a encontrar mejores soluciones para sus pacientes. Formada a partir de la fusión de IMS Health y Quintiles, IQVIA ofrece una amplia gama de soluciones que aprovechan los avances en información, tecnología, análisis e ingenio humano para impulsar la atención médica. Actualmente nos encontramos en la búsqueda de profesionales interesados en ser parte de un gran proyecto con un importante socio de negocios. 🩺 Vacante: Representante de Atención al Paciente – Call Center Tipo de puesto: Jornada completa Modalidad híbrida Zona de trabajo: Col. Nápoles Lunes a viernes 🧑‍⚕️ Descripción del puesto: Estamos en búsqueda de un nuevo integrante para nuestro equipo de Call Center. El objetivo principal del rol es brindar soporte telefónico y digital a pacientes. ✅ Responsabilidades: Atender llamadas entrantes y salientes de pacientes. Brindar información clara y precisa sobre servicios Programas de Soporte a Pacientes. Registrar y actualizar datos en CRM. Resolver inquietudes con empatía, profesionalismo y orientación al paciente. Requisitos: Experiencia en atención telefónica, call center, atención a cliente, etc. Experiencia en programa de soporte a pacientes (PSP). Excelente comunicación verbal y escrita. Manejo de herramientas informáticas y sistemas de gestión (Microsoft Office, CRM). Gran empatía y vocación de servicio. #LI-CES IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Title: Expert Detailing RepresentativeLocation: MauritiusIndustry: Pharmaceutical / HealthcareEmployment Type: Full-Time Overview:A leading global Consumer Healthcare company is seeking a dynamic and experienced Pharmaceutical Sales Representative to join their team as an Expert Detailing Representative (EDR) in Mauritius. This role is ideal for a science-driven sales professional with a strong understanding of healthcare provider (HCP) engagement and a passion for promoting therapeutic solutions that make a difference. Key Responsibilities:As an EDR, you will be responsible for driving HCP awareness, advocacy, and recommendation of key consumer healthcare brands. You will: Conduct expert detailing sessions with HCPs, presenting clinical data and therapeutic benefits.Recruit HCPs to digital platforms and support digital engagement initiatives.Utilize multiple channels (face-to-face, remote, email, webinars) to drive meaningful engagement.Guide HCPs in accessing patient communication tools and digital resources.Encourage participation in Continuous Medical Education (CME) modules.Ensure consistent in-call quality and monitor expert performance metrics.Build and maintain strong relationships with HCPs in your territory.Distribute medical samples to support patient trials and product conversion.Track and achieve KPIs such as AWR, BRMO, and SoR.Meet or exceed territory sales targets.Provide market insights and competitor intelligence to internal teams.Organize and support educational events and meetings.Uphold compliance standards and represent the field team professionally.Qualifications & Requirements: Education: BSc or equivalent in a relevant scientific field.Experience: Minimum 5 years in pharmaceutical sales or a related healthcare role.Skills:Strong communication and presentation abilities.Proficiency in digital tools and CRM systems (e.g., Veeva).Analytical mindset with the ability to interpret sales data and KPIs.Excellent time management and organizational skills.Knowledge of pharmaceutical compliance and ethical standards.Other Requirements:Valid driver’s license and access to a reliable vehicle.Based in Mauritius with the legal ability to work in Mauritius.Why Join Us?This is an exciting opportunity to be part of a forward-thinking team that values innovation, professional development, and impactful healthcare solutions. You’ll play a key role in shaping HCP engagement and driving brand success in a dynamic market. #LI-DNP #LI-CES  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com 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 looking for an opportunity as a Clinical Research Nurse?  Do you want to work for an industry leading company. This part-time role is to support a clinical trial in Marseille where you will need to visit patients in their homes to assist the patient with their medical device. Full training will be given. We are looking for candidates with the following skills and experience: BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedulesBasic knowledge of medical terminologyStrong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and WordExcellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client​Good organizational skills with the ability to pay close attention to detail.#LI-DNP #LI-HCPN #LI-CES #LI-CT1 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 Customer Success Manager to join the Research Practice in the Payers, Providers and Governments group, supporting the growth and adoption of innovative solutions that advance clinical and health research. As a Customer Success Manager you will work closely with clients and IQVIA employees to maximize and expand use and value derived from deployed technology. In this role you will collaborate closely with different IQVIA teams to promote use of our technologies. What we are looking for: BSc in medicine, biomedical sciences, health sciences, pharmacy, or a related field. One to five years of work experience in the health care sector, life sciences or data analytics/data science. More related experience in Project Management and/or Service Delivery is required. Experience with client and stakeholder management and networking. The ability to interact and influence at all levels in both hospitals and in future the IQVIA organisation. Demonstrate a positive and enthusiastic attitude and willingness to help others. Experience with teaching, providing training or hosting workshops and/or providing support and/or coaching to immediate co-workers, employees within the same company or external parties. The ability to translate complicated technical information in a comprehensible way to HCPs, clients and other IQVIA employees. The ability to translate clinical/health care questions and needs from HCPs into a search strategy and query that retrieves patients-of-interest and data-of-interest. Used to working in an interdisciplinary team. Strong written and verbal communication skills in English & German, including ability to train, present and deal tactfully and in a service-oriented way with clients. Nice to have       • An understanding of or experience with searching through, handling and/or analyzing complex (medical) data.      • Knowledge of the structure of electronic health records and how information is recorded by medical professionals. 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.

Sales Account Manager Location: London IQVIA is recruiting for a Medical Device Sales Specialist. In this role you will be responsible for developing sales in strategic accounts across London. You will become an integral part of the sales team, supported by several clinical specialists in servicing your customers and accounts. Achieve agreed objectives and sales targets as outlined in the annual performance cycle.Within allocated geographical region, interact and promote products to key customers and stakeholders in secondary care. Manage territory through the development of comprehensive business plans.  Focus on highest value opportunities to grow and develop new business including taking competitor share and the adoption of new technologies whilst maintaining key customers and core business.Manage and develop accounts and own the relationship between the Company and the customer, ensuring efficient alignment of all efforts to maximise impact of all activities driving growth.What to ExpectYou will build strong networks of relationships that enable the identification of mutually beneficial opportunities to sell key technologies in the surgical procedural environment. Presenting brand value propositions and value-added customer solutions to positively influence buying behaviours.Thereby analysing and interpreting account strategies and plans utilising key systems and data, both internally and externally, where appropriate to gain a broad understanding of the business environment and insights in to account needs.Partner with Professional Education to develop and maintain associated KOL relationships as well as championing the effective use of the Company’s comprehensive Professional Education offering. Ideal Experience:Strong selling skills in the medical device sectorA solid understanding of Account managementPreferred, but not essential, experience working in cardiology med tech and / or electrophysiology.To make a difference in Medical Device Sales, apply today! Please note: sponsorship is not available for this opportunity.   #LI-DNI #LI-CES #LI-WB1 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Project Manager, eCOALocation: UK, home basedWe are seeking a Project Manager to manage delivery of eCOA projects to internal and external clients .                                                       Job OverviewValidates the project scope, plans and schedules for moderately complex projects; adheres to metrics for project success and begins to suggest appropriate metrics; provides input to and applies standards (e.g. delivery process, roles and responsibilities, operational norms, compliance).Responsibility  Manage day to day implementation of eCOA projects Manage internal staff to support customer projects and manage internal service projects Define and monitor project scope, budget, timelines, resources, quality and deliverables for the full project life cycle Ensure the project team adheres to high quality service and all applicable corporate and client policies and standards Regularly review project contract terms and conditions, and project plan to ensure that all assumptions are still valid Work in close collaboration with the internal or external project stakeholders to achieve the study goals Establish strong customer relationships and seek opportunities to increase customer satisfaction and deepen relationships Communicate effectively with customers to identify needs and propose solutions Keep customers well informed on status of internal service efforts and serves as liaison between internal staff and customer Provide technical direction for the development, design, and systems integration for customer engagements Responsible for managing the development, review and approval of project related study documentation during throughout the full life cycle of the project implementation Provide regular updates and reports to Sponsor and IQVIA upper management Conduct regular status meetings, reviewing project schedule, risks, issues and outstanding action items Implement and monitor a risk management plan at the project level (raise to program level, as necessary) Implement corrective actions as needed to maintain project performance • Identifies opportunities for improving and streamlining projects Manage vendor relationship and tasks Manages the Lessons Learned process throughout the project lifecycle Communicate customer requirements to the product management teams, advocate on the customer’s behalf, and communicate the status of enhancement requests to customers Manage project team members across multiple locations and time zones International Travel required as needed   Education, skills and experience required  Bachelor Degree or equivalent   A thorough understanding of Project Management principles - PMP / PRINCE II certification is a plus In-depth project management experience ideally within clinical research Experience and understanding of the clinical research environment and GCP principles Strong leadership, diplomatic and motivational skills Open, transparent and excellent communication skills, fluency in English both verbal and written Proven ability to work creatively and analytically in a problem-solving environment  Excellent in planning, organizing and monitoring Self-motivated, decisive, with the ability to adapt to change and competing demands Able to communicate and deal effectively with all levels of the organization Confident and comfortable with public speaking in front of a large and diversified audience. Ability to adjust presentation material for differing audience Solid technical background, with understanding or hands-on experience in software development and clinical technologies (EDC, eCOA, IWRS etc.) Strong working knowledge of Microsoft Office tools This role is not eligible for UK visa sponsorship. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 86.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für unseren Kunden, ein renommiertes, international agierendes Familienunternehmen, suchen wir zum nächstmöglichen Zeitpunkt einen Pharmaberater (m/w/d) General Medicine / Diabetes Im Gebiet: Speyer, Neustadt a.d.W., Landau i.d. Pfalz Das sind Deine Aufgaben: Durch die intensive Betreuung ausgewählter Ärzte förderst Du die Verordnung Deiner Präparate und trägst so maßgeblich zum Unternehmenserfolg bei. Du setzt als Experte auf der Basis Deines Fachwissens Beratungsstrategien erfolgreich um und überzeugst so Deine Ansprechpartner. Du findest mit Deinen Gesprächspartnern innovative Therapiekonzepte in anspruchsvollen Indikationen. (optional: zum Wohle des Patienten/für den Patienten/und trägst somit zur Gesundheit und dem Patientenwohl bei) Du führst regionale und zentrale Fortbildungsveranstaltungen in enger Abstimmung mit dem Regionalleiter und Deinem regionalen Team durch. Das bringst Du mit: Du hast idealerweise bereits erste Erfahrung im Pharma-Außendienst gesammelt, idealerweise in der Indikation Diabetes. Als durchsetzungsstarke Persönlichkeit und erfahrener Netzwerker verstehst Du es, Dich und Deine Ansprechpartner zu begeistern. Du möchtest etwas bewegen – für Dein Präparat, für Dich selbst und vor allem für betroffene Patienten. Ausgeprägte kommunikative Fähigkeiten sowie die Bereitschaft, eigenverantwortlich und ergebnisorientiert zu arbeiten. Du kannst mit digitalen Medien gut umgehen und hast solide Kenntnisse, um auch englische Fachtexte zu verstehen. Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] #LI-CES #LI-DNP #LI-SS2 #Pharmaberater; #Biologie; #Chemie; #Pharmareferent; #BTA; #CTA; #PTA; #Oecotrophologie; #Pharmazie; #Pharma-Außendienst IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewConduct testing activities in CDMS environment and provide comprehensive testing expertise to the team to produce efficient, quality database that meets customer requirements. Essential Functions• Independently conduct testing activities to validate edit checks, system settings, SAS listings, Transfer Programming and custom reports in platforms including, InForm, RAVE, OCRDC.• Solid understanding of database structure.• Ensure validation processes and best practice guidelines are being followed strictly by self and team.• Solid understanding of documentation requirements and update all relevant documentation in a timely manner.• Communicate status of project to Validation Team Lead/Manager.• Escalate problems to the attention of Validation Team Lead/Manager.• Mentor Associate Validation Analysts in all testing activities.• Conduct Quality Reviews of testing projects on an ongoing basis as applicable.• Provide suggestions for continues process improvement and actively participate and contribute towards process improvement initiatives as assigned.• Understand and comply with core Operating Procedures and Work Instructions (including Best Practice and Guidance documents).• Meet project objectives as assigned by Validation Team Lead/Manager.• Develop and maintain good communications and working relationships with multiple teams across locations. Qualifications• Bachelor's Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology  Req• 1 - 2 years of relevant clinical DB Testing experience in CDMS Platforms and total exp being 2+ yrs Req IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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

Job DescriptionThe Junior Cloud Operations Engineer supports the operation of cloud‑native platforms with a focus on Kubernetes and microservices‑based applications. This role assists with day‑to‑day deployments, monitoring, and operational support of containerized workloads in Azure and/or AWS environments. The position works closely with DevOps and application teams to ensure stable, reliable, and compliant production and non‑production environments. Key Responsibilities Support day‑to‑day deployments of microservices on Kubernetes platforms (e.g., AKS/EKS) across multiple environments.Assist with routine Kubernetes operations, including monitoring workloads, validating deployments, restarting services, and basic troubleshooting.Execute and support application deployments through CI/CD pipelines, Helm charts, and approved deployment configurations.Monitor application and platform health, respond to alerts, and support incident triage and resolution for containerized services.Coordinate with development and DevOps teams during release activities, configuration updates, and environment readiness checks.Support operational maintenance activities such as configuration updates, certificate renewals, and container image updates.Follow defined service management and change processes, ensuring accurate documentation and timely updates.Maintain deployment runbooks and operational documentation to support consistent and repeatable operations. Preferred Qualification Degree / Engineering, Computer Science, Information Technology, or a related field. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Field Sales Associate – UrologyAbout the Role As a Field Sales Associate (FSA) at Boston Scientific, you will play a pivotal role in supporting regional accounts under the guidance of the Region Sales Manager. Working closely with Territory Managers, you’ll help maintain market share across existing accounts while delivering exceptional service and clinical support. This includes conducting in-services and assisting with training initiatives to elevate the team’s performance and customer experience. Key Responsibilities Strengthen key account relationships through regular customer visits, product demonstrations, educational programs, in-services, procedural observation, and issue resolutionEngage with a broad range of stakeholders including physicians, nurses, technicians, materials management, hospital administration, and infection controlCollaborate with Territory Managers, Sales Management, HEMA, and cross-functional teams to assess business conditions and sales trendsDrive utilization of targeted technologies across assigned accountsDemonstrate clinical excellence in relevant disease statesDevelop and execute proactive service plans with the Region Manager and team to maintain market share and enhance customer satisfactionSupport professional education initiatives by participating in on-site and field training workshopsIdentify opportunities to present Boston Scientific solutions that drive regional sales activityProvide timely updates to the Regional Manager on business plans, competitive landscape, and industry trendsManage expense and promotional budgets in accordance with company guidelinesPrepare comprehensive account-level plans aligned with the Urology Division’s strategic goalsLeverage sales enablement tools such as Salesforce and Tableau to optimize performanceMaintain accurate records of expenses, customer interactions, and field reportsSubmit all required administrative documentation promptlyConduct all sales activities in compliance with Travel & Entertainment (T&E) guidelines, AdvaMed policies, and company integrity standardsParticipate in occasional weekend and evening trade shows or meetingsCommit to travel requirements, typically 40–50%Preferred Qualifications Self-starter with strong leadership qualities and high coachabilityProven ability to set priorities and manage time effectivelySkilled in building and maintaining customer relationshipsFlexible and adaptable to change; able to align work with strategic goalsEnergetic, enthusiastic, goal-oriented, and determinedThrives in a fast-paced, competitive environmentRequired Qualifications Minimum 1 year of successful B2B sales experienceCompletion of a formal sales training program or relevant degreeBachelor’s degreeMust reside within the assigned territoryNote: This role is not eligible for visa sponsorship. Candidates must have authorization to work in the US without the need for sponsorship.#LI-CESIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is 70-75,000 annually. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Sind Sie auf der Suche nach einer neuen Chance oder Herausforderung in der klinischen Forschung? Möchten Sie für ein branchenführendes Unternehmen arbeiten? IQVIA sucht derzeit einen **Studienassistentin / Study Nurse (m/w/d)** zur Unterstützung der Durchführung einer klinischen Studie an einem Zentrum in Hannover. Diese Teilzeit-Position ist ab sofort zu besetzen, zunächst befristet bis zum 31.12.2026 Zu den täglichen Aufgaben gehören: Koordinierung klinischer Forschungsstudien und Aufrechterhaltung eines sicheren Studienumfelds gemäß den Gesundheits- und Sicherheitsrichtlinien unter der Leitung und Delegation des Principal InvestigatorsSicherstellung des Wohlergehens der PatientInnen, Eingehen auf deren Belange bei gleichzeitiger Gewährleistung der höchsten QualitätBetreuung der PatientInnen und Unterstützung des Personals bei administrativen AufgabenPflege von Studienprotokollen, Fallberichtsformularen (CRFs), elektronischen Datenerfassungssystemen (EDC) und anderen Studiendokumenten auf dem neuesten StandPlanung und Koordinierung der logistischen Aktivitäten für Studienverfahren gemäß dem StudienprotokollDurchführung der klinischen Vorbereitungen für die Studie, einschließlich der Beschriftung von Probenentnahmeröhrchen und -behältern, der Inventarisierung des erforderlichen Materials und der Einrichtung oder Behebung von Problemen mit der Ausrüstung und/oder der StudieDateneingabe, Überprüfung der Datenqualität und Beantwortung von FragenUnterstützung bei der Aufnahme von PatientInnen in die Studie durch Rekrutierung, Screening und Einweisung gemäß dem StudienprotokollSammeln, Erfassen und Berichten klinischer Daten und Befunde in angemessener Weise in CRFs und Zusammenarbeit mit dem Prüfarzt über studienbezogene unerwünschte Ereignisse und schwerwiegende unerwünschte Ereignisse gemäß dem StudienprotokollKoordinierung mit dem Studienmonitor bei Studienproblemen und effektive Beantwortung der vom Monitor gestellten Fragen.Wir suchen Kandidaten mit den folgenden Fähigkeiten und Erfahrungen: Mindestens zwei Jahre einschlägige Erfahrung; oder eine gleichwertige Kombination aus medizinischer Ausbildung, Schulung und Erfahrung Kenntnisse über klinische Studien, kombiniert mit fundierten Kenntnissen der abteilungs-, protokoll- und studienspezifischen Arbeitsabläufe, Einverständniserklärungen und StudienpläneAusgeprägte IT-Kenntnisse, geübt im Umgang mit MS Windows und Office-Anwendungen wie Access, Outlook, Excel und WordAusgezeichnete zwischenmenschliche Fähigkeiten mit der Fähigkeit, effektive Arbeitsbeziehungen aufzubauen und zu pflegenSehr gute Deutschkenntnisse in Wort und Schrift#LI-CES #LI-XS #LI-HCPN #LI-DNI 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.

#LI-HCPN #LI-CES #LI-DNP #LI-NS1 #LI-Onsite IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewProvide support and guidance to less experienced  members of an HR team in their day-to-day operational roles.  Support  the continuous improvement of the HR function through development and implementation of HR programs in an assigned geography or business line. With limited guidance, provide comprehensive HR support to employees and management across assigned service areas, business units or departments.  As HR Business Partner, with guidance, provide expertise, support and advice to assigned management teams either locally, regionally, globally or by function. Essential Functions Develop strong and effective team relationships with HR specialist functions/Centers of Excellence, e.g., HRPSC, Finance PSC.Support line managers in the process of new employee orientation where appropriate.Provide advice and guidance to more junior members of the HR team as appropriate.Conduct ad hoc reviews as directed and propose recommendations in handling employment legislation, compliance, HR systems, practices and procedures and, with guidance, provide support and education to line management.Participate as assigned, with minimal supervision, in working with senior HR team members for the day-to-day development and implementation of redesign and new local and global HR initiatives.With guidance, provide HR Partnering management coaching and counseling.With guidance, act as Business Partner to assigned business areas.Work with more experienced HR team members on organizational effectiveness and HR partnering change management efforts associated with reorganizations, mergers/acquisitions and transfers to ensure compliance to local legislation.Provide reports and analyses as requested by senior management.Support line managers in the recruitment and selection process where appropriate.Manage HR-related queries and may work independently or in conjunction with senior members of the HR team and line management on issues.Qualifications Bachelor's Degree  Req and 4 years experience within an HR function as generalist or combination of generalist and specialist experience Req OrEquivalent combination of education, training and experience ReqExtensive knowledge of local and relevant employment legislationExpert coaching and counseling skillsEffective leadership skillsExcellent  problem solving, judgment and decision making skillsGood presentation skillsGood influencing skillsGood computer skills, including Microsoft Office applications and HRIS applicationsStrong verbal and written communication skills and very good interpersonal skillsVery high degree of discretion and confidentialityStrong attention to detailGood ability to work in a matrix environmentAbility to lead a projectAbility to establish and maintain effective working relationships with coworkers, managers and clientsProfessional HR accreditation  ReqIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $68,900.00 - $172,400.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

The Associate Director, Product Management, IQVIA Digital, leads product execution for AIMXR’s identity‑resolution and contextual intelligence capabilities. This role manages a team of Product Owners, each responsible for a defined feature set, and partners closely with Product Managers (PMs) to implement the product strategy they define. You will translate strategic direction into prioritized outcomes, maintain high‑quality backlogs, and guide cross‑functional teams (engineering, data science, UX, privacy, and go‑to‑market) to deliver customer value at scale.Key Responsibilities:Team Leadership: Develop and coach Product Owners, each owning a distinct set of features within AIMXR.Establish clear goals, operating rhythms, and delivery standards for the PO team (definition of ready/done, acceptance criteria, discovery cadences).Ensure consistency in requirements quality, backlog hygiene, and release readiness across feature areas.Promote a culture of customer empathy, measurable outcomes, and continuous improvement.Strategy Implementation & Planning: Partner with PMs to understand market problems, target segments, and outcome goals; convert PM‑defined strategy into executable product plans (epics, features, releases).Contribute actionable input during planning (risks, dependencies, sequencing) while keeping alignment with PM‑owned strategy and prioritization.Translate business objectives into clear success metrics and acceptance criteria for delivery teams.Roadmap & Backlog Ownership: Own near‑ and mid‑term roadmaps for assigned AIMXR components; maintain transparent views of scope, dependencies, and release timing.Lead backlog refinement, story mapping, and estimation with engineering; ensure stories are testable, valuable, and trace to outcomes.Make day‑to‑day tradeoffs on scope and sequencing to protect delivery dates and quality, escalating strategic reprioritization decisions to PMs as appropriate.Cross‑Functional Delivery: Partner with engineering, data science, and architecture to shepherd features from discovery through GA; clarify requirements, edge cases, and non‑functional needs.Coordinate with privacy/governance partners to incorporate compliance requirements into definitions of done.Align with documentation, enablement, and GTM teams to ensure feature readiness (release notes, guides, training materials, and internal demos).Customer & Stakeholder Engagement: Serve as a senior product point‑of‑contact for internal stakeholders and select client conversations to explain capability behavior, roadmap intent, and release plans.Collect feedback from users, delivery, and support teams; synthesize into user stories and backlog updates.Validate outcomes post‑launch via telemetry and customer feedback, and feed learnings back into PM‑owned strategy discussions.Measurement & Continuous Improvement: Define and track feature‑level KPIs (adoption, utilization, performance, quality).Run lightweight experiments and A/B validations where applicable; socialize results and next steps.Improve team flow (lead time, throughput, predictability) and strengthen discovery/delivery practices across your PO team.Requirements & Qualifications: To be eligible for this position, you must reside in the same country where the job is located.Bachelor’s degree required.US Remote with approximately 10% travel required.Experience working with enterprise life sciences and pharmaceutical customers or regulated data products.7+ years’ experience as a Product Owner/Senior PO (or equivalent PM role) delivering software/data products at scale with demonstrated success managing and developing Product Owners or similar IC product roles.Strong backlog management, story writing, and acceptance‑criteria discipline; expert in agile/lean delivery practices.Product marketing experience, preferably in AdTech, MarTech, or digital marketing solutions, with exposure to healthcare/life sciences marketing.Proven ability to partner with PMs: executing against strategy, flagging risks, and translating outcomes into releasable increments.Excellent communication and facilitation skills across engineering, data, UX, privacy, and customer‑facing teams.Experience with audience segmentation and targeting products, behavioral data, or digital engagement signals, AI/ML, or predictive modeling (practical application vs theory)Preferred Qualifications: Experience with large‑scale data/analytics platforms, identity resolution, or contextual intelligence.CSPO / CSPM certification for agile/scrum, preferred.Familiarity with cloud data stacks (e.g., AWS, Snowflake) and data governance/privacy considerations.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $88,300.00 - $246,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Required Skills & Experience Technical Skills Expert‑level SAS programming skills.Strong, hands‑on experience with CDISC SDTM, ADaM and TLFs.Proven experience developing safety, PK, and PK/PD ADaM datasets.Experience supporting POPPK/popPD/Exposure Response(ER) dataset creation workflows.Solid understanding of early‑phase clinical trial designs, including:Phase I / First‑in‑HumanCrossover studiesExposure–response analysisPK parameter poolingExperience 8+ years of statistical programming experience in the pharmaceutical or CRO environment.Demonstrated experience as a Lead Programmer or technical lead.Prior experience working in an FSP engagement model preferred.Experience supporting regulatory submissions is required.Soft Skills Strong communication and stakeholder management skills.Ability to work independently while managing multiple priorities.Detail‑oriented with a strong commitment to quality and timelines.Preferred Qualifications Experience supporting Translational Medicine or Clinical Pharmacology groups.Familiarity with internal exploratory analysis and early‑phase decision‑making needs.Exposure to integrated summaries or pooled PK analyses across studies.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $98,200.00 - $273,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA Biotech is hiring for Site Contracts Associate with 1-3 years' experience negotiating clinical site contracts and budget templates. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. Job Overview We are seeking a Site Contract Specialist to support the development and execution of investigator grant estimates and site contracting activities for clinical trials. This role plays a critical part in ensuring timely and compliant study start-up and maintenance by managing financial and operational aspects of site contracts. Essential Functions Develop investigator grant estimates and proposal text to support business development and proposal creation.Utilize and maintain contract and budget templates, systems, tools, and training materials for assigned sponsors, studies, or programs in alignment with the Scope of Work and Project Plan.Collaborate with sponsors, internal stakeholders, and regional/country teams to ensure successful delivery of project scope and compliance with sponsor requirements and RSU Management Plans.Provide specialized operational and financial contracting support to enable efficient trial initiation and maintenance while ensuring regulatory compliance.Assist in the creation and review of scientific, technical, and administrative documentation to support study start-up and ongoing trial activities.Contribute to the collection, analysis, and dissemination of contracting intelligence to support assigned studies and broader organizational needs.Monitor contracting efficiency and adherence to timelines and financial goals; report performance metrics and out-of-scope activities as needed.Ensure compliance with contract management and quality standards. Provide administrative and operational support to contract analysts, managers, and directors.Maintain accurate records in internal systems including CTMS, databases, tracking tools, and project plans.Qualifications Bachelor’s degree in business, life sciences, or a related field preferred.Experience in clinical trial budgeting, contracting, or site management strongly preferred.Strong understanding of clinical research processes and regulatory requirements.Proficiency in Microsoft Office and contract management systems.Excellent organizational, analytical, and communication skills.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $49,200.00 - $123,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA Biotech is seeking Sr. Site Contracts Associate or Site Contracts Associate with 3-5 years' experience negotiating clinical site contracts and budget templates. This role requires candidates who have sponsor facing experience as well. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. Job Overview Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements.  Essential Functions • Develop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process. • Develop contract language, payment language and budget templates as required as applicable to the position • Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy. • Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan. • Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. • Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. • Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required. • Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements • Report contracting performance metrics and out of scope contracting activities as required. • Work with Quality Management to ensure appropriate contract management and quality standards. Mentor and coach colleagues as required including the delivery of training materials as required. Qualifications • Bachelor's Degree Related field. • 3-5-year relevant sponsor or clinical research organization clinical site contracting experience, including demonstrable global and/or regional experience acting as a contract negotiator. Equivalent combination of education, training and experience. • Good negotiating and communication skills with ability to challenge. • Strong legal, financial and/or technical writing skills. • Strong understanding of regulated clinical trial environment and knowledge of drug development process. • Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines. • Knowledge of applicable regulatory requirements, SOPs and company’s Corporate Standards. • Good understanding of clinical trial contract management. • Ability to develop and suggest alternate contracting language, terms, and financial options. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $62,800.00 - $157,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Summary: Connected Devices is one of the most dynamic and interesting areas within the Clinical Research industry. The identification, strategy and management of various devices and their data ingestion modalities to meet the endpoint goals of our customers is ever challenging and exciting.  This highly visible business unit is closely connected to other trial delivery teams within IQVIA.  We work closely with technology partners and our sponsor partners to help speed therapies to market in a global network. We seek highly motivated and accountable people looking for opportunities to impact the business and be part of the solution. At IQVIA, we look at individuals with a focus on continuous learning and career development Purpose: Support the project manager to deliver projects to the sponsor's satisfaction, on time and within budget.  Support all project related activities for assigned projects in accordance with standard operating procedures, policies and practices. RESPONSIBILITIES: Assist the Project Manager in the set-up, planning, implementation and delivery of assigned projects in accordance with the Scope of Work agreed with the Customer.Assist in monitoring and coordinating efforts of cross-functional project teams.Track project progress, identify and evaluate project risks and take advice from superiors on corrective action as appropriate.Attend the ‘End of Project’ review meeting to ensure that all project activities have been completed in full.Prepare and present project information at internal and external meetings, where requiredEnsure that consistent and appropriate project specific guidelines are documented and circulated to all project team members and that the team is well-trained on these guidelines under guidance of the Project ManagerREQUIRED KNOWLEDGE, SKILLS AND ABILITIES: Knowledge of CRO IndustryDemonstrated ability to deliver results to the appropriate quality and timeline metricsGood problem-solving skillsGood teamwork skillsExcellent customer service skillsAbility to work under limited directionStrong software and computer skills, including MS Office applicationsGood ability to prioritize, schedule and organizeGood interpersonal and communication skillsAbility to establish and maintain effective working relationships with coworkers, managers and clientsMINIMUM REQUIRED EDUCATION AND EXPERIENCE: High School Diploma or equivalent Life science or health care related discipline RequiredOne-year related experience Required Or Equivalent combination of education, training and experience Required#LI-Remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $45,300.00 - $113,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Sales Account Manager Location: Ireland IQVIA is recruiting for a Medical Device Sales Specialist. In this role you will be responsible for developing sales in strategic accounts across London. You will become an integral part of the sales team, supported by several clinical specialists in servicing your customers and accounts. Achieve agreed objectives and sales targets as outlined in the annual performance cycle.Within allocated geographical region, interact and promote products to key customers and stakeholders in secondary care. Manage territory through the development of comprehensive business plans.  Focus on highest value opportunities to grow and develop new business including taking competitor share and the adoption of new technologies whilst maintaining key customers and core business.Manage and develop accounts and own the relationship between the Company and the customer, ensuring efficient alignment of all efforts to maximise impact of all activities driving growth.What to ExpectYou will build strong networks of relationships that enable the identification of mutually beneficial opportunities to sell key technologies in the surgical procedural environment. Presenting brand value propositions and value-added customer solutions to positively influence buying behaviours.Thereby analysing and interpreting account strategies and plans utilising key systems and data, both internally and externally, where appropriate to gain a broad understanding of the business environment and insights in to account needs.Partner with Professional Education to develop and maintain associated KOL relationships as well as championing the effective use of the Company’s comprehensive Professional Education offering. Ideal Experience:Strong selling skills in the medical device sectorA solid understanding of Account managementPreferred, but not essential, experience working in cardiology med tech and / or electrophysiology.To make a difference in Medical Device Sales, apply today! Please note: sponsorship is not available for this opportunity.   #LI-DNI #LI-CES #LI-WB1 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.