IQVIA

 The team & the company   IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. With direct access to the world’s most comprehensive healthcare information, analytics and research resources, IQVIA Real World Solutions (RWS) experts design and deliver innovative data– and technology-enabled evidence programs to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. IQVIA RWS is a fast-growing and highly successful consultancy business, focusing upon on delivering tangible business results to our clients who are key decision-makers and business managers across the international pharmaceutical and healthcare industry.   Within the RWS group, the IQVIA Europe, Middle East, Africa (EMEA) Real World Methods and Evidence Generation (RW MEG) team is composed of around 200 highly qualified multi-disciplinary professionals from a variety of disciplines including health economics, statistics, biochemistry, and epidemiology, based in 12 geographies, with projects delivered across >50 countries.  Our clients operate in the life sciences industry, including global top 20 pharmaceutical companies, medical device, and biotech companies, as well as public health providers and regulatory authorities. They are looking for insight and evidence around the safety, efficacy, effectiveness and cost-effectiveness of health care delivery systems, medical devices, and pharmaceutical products spanning the full spectrum of therapeutic and disease areas. Our diverse mix of clients, the breadth of disease areas, as well as increasing access to novel data sources and methodologies provide a constant and rewarding challenge for our people.  For more information about our company please visit our website: https://www.iqvia.com/  Role purpose  This role will offer you the opportunity to support our EMEA Health Economics team as a Consultant Medical Writer and be part of our HTA Evidence & Strategy Centre of Excellence and Value Communications Centre of Excellence.  This role focusses on medical writing for HEOR purposes, where you will be responsible for writing tasks within HEOR projects and work with a senior team to co-manage small workstreams, project tasks and thought leadership initiatives. Typical projects include medical writing for the new EU Joint Clinical Assessment (JCA) dossier, HTA dossiers (e.g., NICE, SMC, NCPE, etc), global value dossiers, protocols and reports for literature reviews, reports for evidence synthesis and health economic modelling studies, and HEOR-focused peer-review manuscripts and conference abstracts. The audience for the project deliverables will be various life-sciences customers as well as healthcare payers, providers, and regulators. You will work within a team of highly experienced health economists and outcomes research specialists providing support across a range of HEOR projects, working in a cross-functional and cross-country project team, providing medical writing, undertaking quality control, and contributing to the management of project delivery (including guiding the work of more junior team members). The role will expose the candidate to the broad range of EMEA RWS offerings in value communications, HTA strategy and HEOR to support in business development opportunities. An ideal candidate will have a good understanding of the matrix structure typical of our clients from the pharmaceutical industry and how to successfully navigate this structure to achieve clients’ aims, as well as proven success in communicating scientific information in a strategic way to optimize a product’s access to markets and reimbursement.   Qualifications and Skills  Previous experience with medical writing is essential for the role. We are looking for proactive individuals with strong analytical and problem-solving skills. Candidates should have a strategic mindset, the ability to identify potential issues and suggest solutions. The ideal applicant should have apt interpersonal skills and the ability to establish relationships with both internal team members and clients. As such, fluency in conversational and business English is essential. The ability to demonstrate this through slide deck development, report writing, and presentations is essential.  We recruit individuals from a variety of backgrounds to join our well-rounded team. If you are motivated, have a passion for healthcare, and strong organisational skills and experience in medical writing we encourage you to apply. The list below should be viewed as a guide rather than a checklist.  Degree in life sciences (or related), epidemiology or health economics and policy, preferably a Master’s degree;  Significant experience in medical writing, including being the primary writer on peer-reviewed publications and HEOR study reports/protocols;  Familiarity with health economics and health technology assessment is a benefit;  Strong written and verbal English communication skills, expertise in scientific writing requirements;   Excellent Microsoft office skills (expert in use of MS Word), and high attention to detail;   Self-motivated with a strong desire to learn quickly and independently, ability to work autonomously with appropriate guidance when needed;  Strong time-management and organisational skills, and flexibility to work in a fast-paced environment;  Interest in data visualisation and presentation;  Keen to work as a member of a diverse, multi-cultural team.  Responsibilities   Write high-quality HEOR study reports and protocols, HTA/GVD dossiers, manuscripts, conference abstracts;  Work with senior team to co-manage small workstreams, project tasks and thought leadership initiatives;  Conduct quality control reviews of HEOR documents and maintaining audit trails of changes;  Mentor and train less experienced Medical Writers;   Contribute to medical writing training initiatives to upskill the team and set quality standards;  Support the team’s Centre of Excellence initiatives.   Please submit your CV in English. Please note that we're not able to sponsor visa for this position. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 88.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dazu gehören integrierte Projektansätze entlang unseres IQVIA-Lösungsportfolios, die wir individuell an Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für einen bundesweiten Teamaufbau im Bereich Gynäkologie suchen wir zum 01.09.2026 mehrere Pharmaberater (m/w/d). Im Gebiet: Großraum München Rollenbeschreibung Verantwortung für definierte gynäkologische Zielkunden und Aufbau nachhaltiger KundenbeziehungenUmsetzung des Markteintritts im Bereich Women’s Health auf GebietsebenePositionierung des Produkts sowie Durchführung fundierter FachgesprächeAufbereitung und Präsentation klinischer StudiendatenEntwicklung und Umsetzung individueller Account-PläneSteuerung der Gebietsperformance unter Nutzung von CRM-Tools (z. B. Veeva)Enge Zusammenarbeit mit internen Schnittstellen unter Einhaltung von Compliance-Vorgaben​Erforderliche Qualifikationen Ein abgeschlossenes Studium in Naturwissenschaften oder eine vergleichbare Qualifikation nach §75 AMGGültiger Führerschein sowie Reisebereitschaft innerhalb des jeweiligen GebietsErfahrung oder Kontakte im Bereich Gynäkologie / Women’s Health bevorzugtSicherer Umgang mit Compliance-Vorgaben (inkl. SAMs)Ausgeprägte Kundenorientierung und überzeugendes AuftretenSensibilität und Offenheit im Umgang mit Women’s Health ThemenErfahrung mit CRM-Systemen (z. B. Veeva) von VorteilGute Englischkenntnisse von VorteilDas 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 KrankenzusatzversicherungenEin top ausgestatteter Firmenwagen mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des ModellsEine moderne IT-Ausstattung für Deinen modernen digitalen ArbeitsplatzUnser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige PerspektiveWir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines WohnortsVielfältige 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 BeschäftigungsverhältnissesUnser 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 #PharmaceuticalSales #PharmaRepresentative #Pharmacy #FieldSales #Gynäkologie#Woman’s Health 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.

Purpose The Investigator Payments Analyst is accountable for budget planning, analytics and payment execution in a direct country or extended country group (OPC and satellite countries) in close collaboration with the SSO Study Start-Up Managers, SSO Clinical Project Managers and SSO Contracting Specialists in compliance with GCP/ICH, and regulatory requirements. Accountabilities Supports country SSU strategy in close collaboration with SSO Study Start-Up Team Lead and SSO Study Start-Up Managers to ensure SSU timelines and deliverables are met according to country commitments. Responsible for accounting and execution of investigator payments in a direct country or extended study group (OPC and satellite countries) in close collaboration with SSO Study Start- Up Manager, SSO Clinical Project Manager and SSO Contracting Specialist in assigned projects. Project controlling & budget management supports financial planning, forecasting and management, analyses, and reports project costs and their drivers. Set-up & validation of investigator contracts in the accounting system for clinical studies. Executes and monitors internal controls. Translates Grant Plans into local Payment Schemes. Prepares and submits country TCF(s). Updates systems (ACT, Optimus, etc.) Executes payments, communicates with sites when it comes to payment issues. Tracks and oversees payment status. Ensures adherence to financial standards, prevailing legislation, ICH/GCP, IRB/IEC, Health Authority and SOP requirements. Implements innovative and efficient processes. Activities & Interfaces Externally facing role with impact on Principal Investigators and Institution/Site business offices. Internal partnerships with Trial Grants Experts to ensure appropriate feedback and Grant Plan leveling for sites. Key Performance Indicators Performance against budget planning and payment commitments at the country level. Delivery of  study milestones  in adherence  with prevailing  legislation, ICH/GCP, IRB/IEC, Health Authority and SOP requirements Timely submission and delivery of high-quality clinical trial documentation/data. 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 €38 000,00 - €57 000,00. 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.

We are seeking Lab Project Services Coordinator to join IQVIA Laboratories at Marietta, GA.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary:Support the Project Manager and broader project team by coordinating routine laboratory project activities across the full study lifecycle, from start-up through close-out. Help ensure study deliverables are completed efficiently, accurately, and in line with standard operating procedures, protocol requirements, and customer expectations. What You'll Be Doing:Support study start-up activities by preparing meeting minutes, action logs, and protocol-specific laboratory instruction documentsCoordinate routine study tasks such as site loading, Investigator Portal access, kit shipments, and day-to-day study monitoringUse status reports, monitoring tools, and study outputs to identify trends and provide feedback on site and service performancePartner with internal and external stakeholders to resolve protocol questions, queries, issues, and escalations in a timely mannerLead customer communications and support project-related activities when the Project Manager is unavailableAssist with project close-out activities and help ensure study documentation and deliverables are completed appropriatelyParticipate in meetings, audits, inspections, and study training activities with sites, CRAs, and customers What We Are Looking For:High School Diploma or equivalent required; Bachelor’s Degree in life sciences or related field preferred1+ years relevant experience (Clinical, Medical or Healthcare industry preferred)Computer proficiency in word processing, presentation and spreadsheet applicationsAbility to use monitoring tools, status reports, and study outputs to support study performance tracking and issue resolutionOther Equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Strong interpersonal, written, and verbal communication skills with a good command of EnglishStrong organizational and time management skills with the ability to manage multiple competing prioritiesDemonstrated critical thinking and problem-solving ability in a fast-paced environmentAbility to establish and maintain effective working relationships with coworkers, managers, customers, and study stakeholdersAbility to lift up to 50 lbs, frequent standing and walking, occasional sitting, close eye work requirement (computer, typing, reading small prints). Physical demands vary depending on assigned work area and work tasks. Occasional exposure to cold temperatures. What We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.To learn more about our benefits, visit https://jobs.iqvia.com/benefits.If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $44,500.00 - $92,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

We are seeking Associate Laboratory Project Services Manager to join IQVIA Laboratories at Marietta, GA remotely.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary:Under general direction, manage all laboratory aspects of clinical trial projects, serving as the main point of contact for customers throughout the study lifecycle. Ensure studies are delivered in alignment with standard operating procedures, policies, and best practices. What You'll Be Doing:Lead study setup activities including protocol and budget review, project planning, and risk and issue trackingCoordinate with study setup teams to ensure quality database configuration and protocol-specific documentationMonitor project timelines, deliverables, and documentation across the full study lifecycle including eTMF managementManage study scope changes, budgets, and service quality while implementing improvements as neededAct as the primary customer contact, building strong relationships and facilitating clear communicationCoordinate and resolve study-level issues, acting as an escalation point when requiredRepresent the company at investigator meetings, audits, and training sessions for sites and stakeholdersSupport continuous improvement initiatives and assist in training less experienced team members What We Are Looking For:Bachelor's Degree in Life Sciences and/or related field preferred2+ years of clinical or research industry experience, including 1 year project management / project set up experience Pref Or Equivalent combination of education, training and experienceWorking knowledge of central laboratory operations including logistics, specimen management, and data reportingProficiency in Microsoft Office and experience with centralized laboratory or project management systemsOther Equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Strong interpersonal and customer relationship management skillsAbility to manage multiple priorities in a fast-paced environment while meeting deadlinesEffective written and verbal communication skills with strong attention to detail What We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey. To learn more about our benefits, visit https://jobs.iqvia.com/benefits. If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $64,200.00 - $133,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Track, analyze, and interpret changes in PhilHealth, eSOA, DOH, and related regulations impacting HIS.Define system scope, objectives, and regulatory impact through detailed research and fact‑finding.Act as primary owner for regulatory interpretation and clarification."Develops or modifies moderately complex information systems.Includes analysis of business and user needs, documenting requirements, and revising existing system logic difficulties as necessary.Guides and advises less-experienced Business Systems Analysts.Competent to work in some phases of systems analysis and considers the business implications of the application of technology to the current business environment.Qualifications Bachelor's Degree Computer Science or Business Administration, or equivalent experienceTwo (2) years experience in systems analysisKnowledge of business-wide applications (e.g. third party software internal operational applications, etc.) or IQVIA client facing applications and productsDemonstrated ability to understand client requirements and as well as underlying infrastructure applications, systems and processes to enable execution of those 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.

The Team IQVIA is a fast-growing and highly successful consultancy business, focusing on delivering tangible business results to our clients who are key decision-makers and business managers across the international pharmaceutical and healthcare industry. With direct access to the world's most comprehensive healthcare information, analytic and research resources, IQVIA experts design and deliver innovative, data- and technology-enabled evidence programmes for the pharmaceutical industry. We apply scientific rigour and advanced analytics to real-world data to help our clients improve healthcare. The IQVIA Global Health Economics and HTA team includes highly qualified multi-disciplinary professionals in a variety of health economics, statistics, life sciences and epidemiology-related disciplines based across multiple geographies worldwide. We help our customers design and execute an evidence generation strategy meeting payer and health technology assessment (HTA) evidence requirements and effectively communicate their product's value story. Our clients operate in the life sciences industry, including the global top 20 pharmaceutical companies, medical device and biotech companies, as well as public health providers and regulatory authorities. They are looking for insight and evidence around the safety, efficacy, effectiveness and cost-effectiveness of healthcare delivery systems, medical devices, and pharmaceutical products spanning the full spectrum of therapeutic and disease areas. Our diverse mix of clients, the breadth of disease areas, as well as increasing access to novel data sources and methodologies provide a constant and rewarding challenge for our people. For more information about our company please visit our website: https://www.iqvia.com/ Role Overview This is a manager role within the IQVIA Global Health Economics and HTA team with a focus on health technology assessment (HTA) and strategic offerings to support our clients with designing an evidence generation and dissemination strategy for their products that meets HTA requirements and optimises the chances for market access. The primary focus of this role is on UK HTA, supporting submissions and engagements with agencies such as NICE and the SMC, although there is flexibility to work on other types of products and geographies should the opportunity arise. The successful candidate will: Be involved in shaping and leading the team and offerings, working closely with the wider senior leadership team and centres of excellence across the global network Manage business development, from proactively developing client relationships to understanding their strategic goals and milestones, with senior oversight; confirming, managing and maintaining the scope of the project to meet those goals in a timely and efficient manner Manage HTA project strategy and direction, with a particular emphasis on UK HTA processes and requirements, with senior oversight; identifying potential challenges to product value, and the development of risk mitigation strategies, as appropriate Manage the project delivery team on a range of projects, including dossier development and submission support for UK HTA agencies, early scientific advice, informing and defining HTA strategy and other strategic HTA offerings to support our clients, with senior oversight. There will also be opportunities to contribute to multi-country and global HTA projects Involvement in mediating, negotiating and problem solving, within and outside of the immediate project team, with senior oversight Train and identify opportunities for more junior members of the team to support their career development as HTA specialists Work within and across internal IQVIA teams, including technical consultants responsible for studies generating HTA evidence and complementary functions such as Market Access, Patient-Centered Solutions, HTA Accelerator Solutions, database studies and local teams across the global network Liaise with clients who will include pharmaceutical, biotechnology and medical devices companies with global and regional headquarters, and occasionally their affiliate teams Support and/or lead thought leadership for HTA topics, such as preparing conference abstracts and posters, supporting development of white papers and peer-reviewed publications on HTA and guiding interns working with the team on HTA-focused thesis topics Provide line management, depending on interests The demand for IQVIA's HTA offerings has seen dramatic increases over the past two years and will continue to expand in response to evolving HTA processes globally, including the growing importance of UK HTA. The role of the Senior Consultant is a management role within the IQVIA Global Health Economics and HTA team and is expected to play an important role in shaping the team's UK HTA offerings. There will also be opportunities to expand your portfolio into other areas if desired. The role is based in either Spain, Greece, Portugal or South Arica, with flexibility regarding frequency of office and home working. Please refer to our diversity and inclusion statement for further information. The Successful Candidate We are looking for a candidate with a good mix of academic and professional experience, domain experience, and interpersonal skills. An ideal candidate has experience with UK HTA submissions and preparing for and supporting early HTA scientific advice, as well as proven success in navigating HTA processes in a strategic way to optimise a product's access to markets and reimbursement. Experience with multi-country HTA submissions is also highly desirable. Experience with statistical methods used in clinical trials and evidence synthesis is highly desirable. The ideal candidate will also have a good understanding of the structure typical of our clients from the pharmaceutical industry and how to successfully navigate this structure to achieve client's aims. The list below should be viewed as a guide rather than a checklist. Qualifications and Desired Experience Postgraduate degree level education or higher from a relevant discipline (such as, but not limited to, HTA, health economics, economics, life sciences, epidemiology, biostatistics, public health, medicine, pharmacy, etc.) AND at least 4 years of relevant work experience (such as, but not limited to, pharmaceutical sector, consulting, academia) with preparing evidence submissions aligned to the HTA processes and requirements within the UK and/or Europe as well as involvement in the appraisal and negotiation processes, where relevant Demonstrable commercial awareness and thorough understanding of the pharmaceutical industry, with an existing network of HEOR contacts highly desirable Project management experience, including managing multidisciplinary teams Strategic thinking and attention to detail Previous experience in a consultancy environment is highly desirable Commercial acumen and proven consultancy skills is highly desirable Strong written and verbal communication skills with fluency in English – applications should be sent in English Strong understanding of the design of clinical trials, statistical methods used in clinical trials, and methodology for evidence synthesis is highly desirable Quantitative skills, including biostatistics and health economic modelling methods and good knowledge of statistical software packages (e.g., STATA, R) is desirable but not essential Please submit your CV in English. Our Commitment to You IQVIA are committed to your professional growth in the healthcare industry. During the first three months new joiners will be supported with a structured onboarding programme to ensure a smooth transition into the team and the wider organisation. IQVIA offers numerous training opportunities. As a Senior Consultant you will have opportunities for external trainings aligned with business and team objectives. IQVIA also offers unlimited access to eLearning courses on LinkedIn Learning and Learning Edge (our internal training platform). The organisational structure of the team ensures that each team member can have regular 1:1 meetings with their line manager. These meetings range from goal setting to advice for projects; the common theme is to provide personalised development support. You will be rewarded with a competitive salary, bonus, and benefits. You will have the opportunity to gain invaluable and transferable experience within an innovative team with a global footprint. Your new role offers flexibility, including remote working and occasional office visits. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies. IQVIA 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 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.

¿Quieres iniciarte en el mundo de la visita médica dentro de la industria farmacéutica?IQVIA es líder mundial en el uso de datos, tecnología, analíticas avanzadas y experiencia humana para ayudar a sus clientes a impulsar el cuidado de la salud. Junto a las empresas a las que prestamos servicios, estamos habilitando un sistema de salud más moderno, más efectivo y más eficiente, a la vez que creamos soluciones innovadoras para transformar los resultados de las compañías y de los pacientes.Seleccionamos un Delegad@ de Venta farmacia para dar una oportunidad a profesionales que quieran ganar experiencia e introducirse en el área comercial de la industria farmacéutica.Deberás realizar visitas de farmacia en tu zona asignada con el fin de conseguir los objetivos marcados.El puesto requerirá que adoptes un enfoque amplio del negocio, así como un alto nivel de autonomía e independencia.Si tienes experiencia comercial y ganas de entrar o continuar desarrollándote en la industria farmacéutica, ¡Esta es tu oportunidad! #LI-CES #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Te apasiona la venta y el contacto directo con farmacias? 🚀 ¿Eres un perfil claramente comercial y orientado a resultados? ¡Esta es tu oportunidad!Buscamos un/a Delegado/a de Ventas con experiencia en canal farmacia 💼 para gestionar la zona de Valencia, Alicante y Murcia, con base en Valencia, incorporándose a un proyecto dinámico y en crecimiento 📈.Tu día a día estará enfocado en la gestión y desarrollo de la cartera de farmacias 🤝, identificación de oportunidades de negocio, negociación y cierre de acuerdos, con un claro enfoque a resultados y posicionamiento de producto en el punto de venta.Buscamos una persona con alta capacidad comercial 🔥, proactiva, ambiciosa y acostumbrada a trabajar por objetivos, que destaque por su habilidad para generar relaciones de confianza con el cliente y dinamizar las ventas en su zona.Se ofrece la oportunidad de formar parte de un proyecto estable, con recorrido y potencial de crecimiento 🌱, donde podrás desarrollar al máximo tu perfil comercial.Si buscas un entorno donde potenciar tu perfil comercial, asumir retos y crecer profesionalmente, queremos conocerte 💼✨📩¡Da el siguiente paso en tu carrera y únete a un proyecto con impacto real en farmacia! 🚀Requisitos🎯 Perfil que buscamos-Formación universitaria en Ciencias de la Salud.-Experiencia mínima de 2 años como delegado/a de visita a farmacia.-Residencia en la zona de influencia.-Carnet de conducir y disponibilidad para desplazarte dentro del territorio asignado.💡 Competencias clave para brillar en este rol-Excelente comunicación y capacidad para generar relaciones de confianza.-Orientación al cliente y sensibilidad hacia sus necesidades.-Fuerte capacidad de análisis para entender el negocio y detectar oportunidades.-Planificación y organización para gestionar eficientemente tu zona.-Espíritu de trabajo en equipo, sumado a una actitud proactiva e iniciativa constante.-Clara orientación a resultados y motivación para alcanzar objetivos comerciales.Tipo de contrato:Temporal 6 meses con posibilidad de continuidadNúmero de vacantes:1Remuneración anual:19.000 € brutos fijo año & 30.000 € Incentivos#LI-CES #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Te apasiona la venta y el contacto directo con farmacias? 🚀 ¿Eres un perfil claramente comercial y orientado a resultados? ¡Esta es tu oportunidad!Buscamos un/a Delegado/a de Ventas con experiencia en canal farmacia 💼 para gestionar la zona de Valencia, Alicante y Murcia, con base en Valencia, incorporándose a un proyecto dinámico y en crecimiento 📈.Tu día a día estará enfocado en la gestión y desarrollo de la cartera de farmacias 🤝, identificación de oportunidades de negocio, negociación y cierre de acuerdos, con un claro enfoque a resultados y posicionamiento de producto en el punto de venta.Buscamos una persona con alta capacidad comercial 🔥, proactiva, ambiciosa y acostumbrada a trabajar por objetivos, que destaque por su habilidad para generar relaciones de confianza con el cliente y dinamizar las ventas en su zona.Se ofrece la oportunidad de formar parte de un proyecto estable, con recorrido y potencial de crecimiento 🌱, donde podrás desarrollar al máximo tu perfil comercial.Si buscas un entorno donde potenciar tu perfil comercial, asumir retos y crecer profesionalmente, queremos conocerte 💼✨📩¡Da el siguiente paso en tu carrera y únete a un proyecto con impacto real en farmacia! 🚀Requisitos🎯 Perfil que buscamos-Formación universitaria en Ciencias de la Salud.-Experiencia mínima de 2 años como delegado/a de visita a farmacia.-Residencia en la zona de influencia.-Carnet de conducir y disponibilidad para desplazarte dentro del territorio asignado.💡 Competencias clave para brillar en este rol-Excelente comunicación y capacidad para generar relaciones de confianza.-Orientación al cliente y sensibilidad hacia sus necesidades.-Fuerte capacidad de análisis para entender el negocio y detectar oportunidades.-Planificación y organización para gestionar eficientemente tu zona.-Espíritu de trabajo en equipo, sumado a una actitud proactiva e iniciativa constante.-Clara orientación a resultados y motivación para alcanzar objetivos comerciales.Tipo de contrato:Temporal 6 meses con posibilidad de continuidadNúmero de vacantes:1Remuneración anual:19.000 € brutos fijo año & 30.000 € Incentivos#LI-CES #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human ingenuity to drive healthcare forward. Outcomes Assessments (COAs) organization leads the industry in generating data to ensure that the patient voice is incorporated into the development and commercialization of medication and other drug/non-drug interventions. We focus on understanding and meeting the needs of our clients – mostly life science/pharmaceutical companies – through the application of broad consulting expertise and technical scientific knowledge to conduct scientifically rigorous research. This research is broad and includes qualitative (e.g., interviews, focus groups), quantitative (e.g., clinical outcome assessments/patient-reported outcomes (PROS), preference research) and passive (e.g., digital health technology tools) approaches to understand patient, caregiver, and healthcare professional experiences and expectations of disease and treatment. To meet our client expectations and retain the excellent reputation built up over time the IQVIA COAs team is committed to recruiting, training and supporting driven individuals who have life science, consulting, and/or product development skills that can be applied to COA research activities. Individuals joining us are assured of a rewarding and progressive career in patient-focused research. You’ll have the opportunity to address challenging client issues, across multiple geographies with a hands-on influence in developing and delivering solutions.  We operate in a truly multi-cultural, collegial and collaborative work environment that is rich in development and growth. Role & Responsibilities •    Serve as the primary account manager for COA Accelerator clients, managing onboarding and ongoing support.•    Deliver training sessions (live and recorded) to ensure effective platform use.•    Drive customer success initiatives, monitoring engagement and proactively addressing challenges.•    Collect client feedback and collaborate with product teams to suggest enhancements based on pain points.•    Identify opportunities to expand collaboration within COA Accelerator, Instrument Services, PCS, and other IQVIA offerings.•    Support prospecting and business development in partnership with internal IQVIA stakeholders.•    Assist in marketing activities, including webinars, case studies, and promotional campaigns.•    Contribute to proposal development, presentations, demos, and trial setups for prospective clients.•    Participate in offering development, helping refine COA Accelerator and related services. Skills & Qualifications - our ideal candidate will have: •    Degree in Life Sciences or related field. •    3 years of experience in a consulting / advisory / strategy role in the COA / PRO space (working either in industry, CROs, or consultancies) •    Strong client-centric mindset with proven ability to build and maintain relationships.•    Previous consulting, sales or business development experience (account management, customer success, or similar roles are a plus)•    Deep knowledge of Clinical Outcome Assessments (COAs), Patient Experience Research and associated services.•    Excellent communication and interpersonal skills.•    Proficiency in PowerPoint and ability to deliver compelling presentations.•    Strong organizational and time management skills.•    Ability to work independently in a remote environment and collaborate across global teams.  Additional Requirements •    Familiarity with subscription-based SaaS platforms and digital adoption strategies.•    Understanding of clinical trial processes and COA-related regulatory considerations.•    Ability to analyse usage data and generate insights for client engagement.•    Comfort with virtual training tools (Zoom, Teams, etc.).•    Significant experience leveraging AI tools for work.•    Fluency in English. THIS ROLE IS NOT OPEN TO 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.

Team  IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. With direct access to the world’s most comprehensive healthcare information, analytics and research resources, IQVIA Real World Solutions (RWS) experts design and deliver innovative data– and technology-enabled evidence programs to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients.      Within the RWS group, the IQVIA Europe, Middle East, Africa (EMEA) Real World Methods and Evidence Generation (RW MEG) team is composed of around 90 highly qualified multi-disciplinary professionals from a variety of disciplines including health economics, statistics, epidemiology and data management, located across 8 geographies.   Our clients operate in the life sciences industry, including the global top 20 pharmaceutical companies, medical device and biotech companies, as well as public health providers and regulatory authorities. Our clients look for insight and evidence on the safety, efficacy, effectiveness and cost-effectiveness of health care delivery systems, medical devices, and pharmaceutical products spanning the full spectrum of therapeutic and disease areas. Our diverse mix of clients, the breadth of disease areas as well as increasing access to novel data sources and methodologies provide a constant and rewarding challenge for our people.    For more information about our company please visit our website: https://www.iqvia.com     Role overview  In this role within the EMEA RW MEG you will be producing materials and services relating to the Health Economics Outcomes Research business areas (health economic modelling, evidence synthesis, statistical analysis, health technology assessment submissions, report and publication development for value communication) that generate value for our clients. The role of the Consultant is expected to play an important role in shaping the team’s literature review offerings.   The successful candidate:  Will be involved in shaping and leading the team and offerings, working closely with the EMEA RWS Center of Excellence for Systematic Literature Review and the wider senior leadership team  Has a good understanding of systematic literature methods (e.g., Cochrane)  Can independently develop searches in various databases (e.g., EMBASE, MEDLINE, Cochrane, PubMed, etc.) and proficient in using OVID SP or another similar platform  Keeps up to date on new methodologies and HTAs requirements for systematic literature reviews and be an in-house go-to expert for the team  Has a good understand of different types of literature reviews (e.g., systematic, targeted, pragmatic, etc.)  Manages literature review projects with senior oversight  Guides the team on interpretation/qualitative synthesis of the literature review findings   Oversees literature review projects that meet rigorous HTA requirements, conducts quality control of literature review deliverables (searches, screening files, extractions, reporting)  Is a day-to-day contact with clients who will include pharmaceutical, biotechnology and medical devices companies with global and regional headquarters based in the EMEA region, and occasionally their affiliate teams, with senior oversight  Oversees the development of research questions, PICOS criteria, search strategies and literature review protocols   Contributes to business development as well as internal initiatives for the advancement of innovative methodological approaches   Collaborates with other business areas and functions of the organisation to deliver client services and support the development of new offerings  Qualifications and desired experience We are looking for a candidate with a good mix of academic and professional experience, domain experience and interpersonal skills. An ideal candidate has a good knowledge of literature review methods and has experience in conducting rigorous literature reviews in health sciences. The ideal candidate will also have a good understanding of the typical structure of our clients from the pharmaceutical industry and how to successfully navigate this structure to achieve client’s aims.   The list below should be viewed as a guide rather than a checklist. We want to prioritise recruiting candidates who will incorporate IQVIA’s value of ‘brave minds’ with their previous experience to put a personal spin on this role. If you share our passion for driving healthcare advancements through unparalleled data and have a passion for collaboration and solving complex problems, we encourage interested candidates who feel like they could be a good fit for the role to apply.  Desired skills and qualifications:   Postgraduate degree level education or higher from a relevant discipline such as health or bioscience-related, medicine, biomedical sciences, health economics, health policy, epidemiology, public health, or information science  Prior relevant experience, >2 years (such as, but not limited to experience in systematic literature reviews and/or meta-analyses)  Understanding of research principles, PRISMA principles, Cochrane guideline for SLRs, methods of the assessment of risk of bias for different study designs  Understanding of the principles of evidence-based healthcare, critical appraisal and the interpretation and synthesis of health care research   Understanding (and experience is advantageous) with the HTA agency requirements for evidence reviews and synthesis  Excellent oral and written communication skills  Accuracy, attention to detail and time management skills  An understanding of meta-analysis methods is advantageous, but not essential  Strong written and verbal communication skills with fluency in English  Demonstrable commercial awareness and thorough understanding of the pharmaceutical industry is advantageous   Proficiency in MS Word, PowerPoint, Excel  Eligibility to work in one of our office locations without visa sponsorship   Please submit your  CV in English. 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.

Mitarbeiter Mitarbeiterversorgung ( m/ w/ d) Wirke mit an der digitalen Transformation in der Gesundheitswirtschaft und profitiere von einer gesicherten wirtschaftlichen Perspektive. Neben anspruchsvollen und abwechslungsreichen Aufgaben mit genügend Freiraum für selbstständiges Arbeiten sowie der Mitarbeit in einem engagierten und motivierten Team. Was dich bei uns erwartet: • Mindesteinstiegslohn 14,50 €/ Stunde • Durch unsere Trainer und Mentoren Programm ist eine strukturierte Einarbeitung garantiert und Du bekommst regelmäßiges wertvolles Feedback • Es gibt eine faire Überstundenregelung mit Freizeitausgleich oder einer Vergütungsmöglichkeit ( 25 % Zuschlag bei Vollzeitbeschäftigung ) • Du kannst interne Entwicklungsmöglichkeiten, wie individuelle Weiterbildungen, Workshops und Seminare nutzen sowie eigene Seminarwünsche einbringen • Unsere Kantine bietet kostengünstiges Essen u.a. warmes Mittagessen für 1,30 € • kostenlose Kalt- und Heißgetränke u.a, Fanta, Cola, Sprite, heiße Schokolade, Kaffee Tee, sowie auch kostenloses Obst für alle Beschäftigten • Betriebliche Altersvorsorge • kostenlose Lebensberatung von TALINGO EAP • betriebliches Gesundheitsmanagement • kostengünstiger Parkplatz in Büro Nähe • rabattiertes Jobticket • regelmäßige Unternehmensevents wie u.a. Grillfeste, Weihnachtsfeiern Werde Teil unseres Teams und freue Dich auf ein dynamisches Umfeld und spannende Aufgaben. Aufgaben: • Fachliche und organisatorische Mitarbeit in der Mitarbeiterversorgung • Herstellung und Zubereitung aller benötigten Speisen sowie Sicherstellung der Qualität und Quantität des gesamten Leistungsangebotes • Erwärmen, Präsentieren und Ausgabe der Komponenten der Warmspeisen ohne Qualitäts- und Quantitätsverlust • Vor- und Nachbereitungsarbeiten im Produktionsbereich der Küche sowie in den Kantinenräumen • Entgegennahme, Kontrolle und fachgerechte Lagerung der Verbrauchsgüter • Überwachung der Lagervorräte, der Verfallsdaten und der daraus resultierenden Maßnahmen •Reinigung der Küchengeräte und Kantinenräume •Ordnungsgemäßes Bedienen der Spül- und Reinigungsmaschinen • Sicherstellung eines reibungslosen und schnellen Serviceablaufs • Einhaltung der Unfallverhütungsvorschriften und des HACCP-Konzepts inklusive Tragen von Arbeitsschutzkleidung •Entgegennahme von positiven und negativen Feedback und Einleiten entsprechender Maßnahmen •Einhaltung der innerbetrieblichen und gesetzlichen Datenschutzregelungen innerhalb der Fachgruppe • Im Bedarfsfall Erledigung anderer zumutbarer Aufgaben und Tätigkeiten, die von den Fähigkeiten und Fertigkeiten her ausführbar sind Voraussetzungen: • Für die Arbeit in unserem Team, benötigst du ein gültiges Gesundheitszeugnis/Lebensmittelpass. • Vorkenntnisse aus der Hotellerie bzw. Gastronomie sind von Vorteil oder du verfügst über Erfahrungen als Haushaltshilfe, Küchenhilfe oder Hauswirtschafter (m/w/d). • Du bringst ein gepflegtes Erscheinungsbild mit, hast Spaß an Ordnung und Sauberkeit und besitzt eine gründliche und zügige Arbeitsweise. • Für deinen professionellen Einsatz erhältst du von uns selbstverständlich die vollständige Arbeitskleidung. • Du kannst uns von Montag bis Freitag im Zeitraum von 05:00 Uhr bis 17:00 Uhr (Schichtsystem) zur Verfügung stehen. 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.

database processing problems considering computer equipment capacity and limitations, operating time and form of desired results. Essential Functions• Assists with database design or modifications to solve database processing problems considering computer equipment capacity and limitations, operating time and form of desired results.• Performs the administration, monitoring, tuning and support of databases in the production environment.• Implements database setups of development, user acceptance test and production  environments.• Implements  backups and recovery procedures.• May participate in database analysis and database design tasks to meet required operational standards and performance levels (as measured by reliability, response time, query execution time, etc.).• May participate in database consultations and database design reviews.• Activities may include: denormalization, developing data archival schemes, sizing, creation of data definition language and database objects, referential integrity and security enforcement and application optimization. Qualifications• Bachelor's Degree Computer Science, a related field, or equivalent experience Req• One (1) year experience in the database administration area Req• Ability to work collaboratively in a team environment. Ability to carry out moderate analysis and information gathering to resolve problems on non-routine matters. 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 OverviewThe Associate Software Engineer supports the design, development, and maintenance of software solutions, working across both front-end and back-end layers. This role is ideal for early-career professionals, focusing on building foundational technical expertise while contributing to the enhancement of IQVIA’s platforms. The individual will collaborate with cross-functional teams, troubleshoot issues, and ensure code quality aligns with industry and organizational standards.Job ResponsibilitiesAssist in the design and development of scalable software solutions with guidance from senior engineers.Develop, test, and maintain efficient, reusable, and reliable code.Work across the full application stack, including front-end (UI) and back-end components.Analyse software requirements and translate them into technical solutions.Perform unit testing and support system validation processes.Troubleshoot, debug, and resolve software defects and performance issues.Participate in code reviews and contribute to improving development standards.Review functional specifications and validation deliverables as assigned.Support small-scale development projects under supervision with defined instructions.Contribute to technical documentation, including design and implementation details.Continuously learn and apply industry best practices and IQVIA quality standards.Required Qualifications and ExperienceBachelor’s Degree in Computer Science, Computer Engineering, or a related field (or equivalent practical experience).1+ years of relevant experience in software development Basic understanding of software development lifecycle and programming concepts.Familiarity with object-oriented programming principles.Exposure to relational databases and basic SQL queries is preferred but not mandatory.Technical SkillsProficiency in JAVA programming languageKnowledge of web technologies such as HTML, CSS, and JavaScript.Familiarity with modern frameworks like React.js and Node.js (preferred).Understanding of SQL and database concepts.CompetenciesStrong problem-solving and analytical thinking skills.Critical thinking and attention to detail.Ability to learn quickly and adapt to new technologies.Effective communication and collaboration skills.Basic understanding of coding standards and best practices.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. Collaborate and liaise with study team members for project execution support as appropriate. If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications Bachelor's Degree in scientific discipline or health care preferred. Requires at least 1 year of on-site monitoring experience. Equivalent combination of education, training and experience may be accepted in lieu of degree. Req Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Good therapeutic and protocol knowledge as provided in company training. Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). Written and verbal communication skills including good command of English language. Organizational and problem-solving skills. Effective time and financial management skills. Ability to establish and maintain effective working relationships with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Home Based role requiring local submissions experience and fluency in Turkish language.  Essential Functions Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.Perform start up and site activation activities according to applicable regulations, SOPs and work instructions.Distribute completed documents to sites and internal project team members.Prepare site regulatory documents, reviewing for completeness and accuracy.Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.Review and provide feedback to management on site performance metrics.Review, establish and agree on project planning and project timelines.Ensure monitoring measures are in place and implement contingency plan as needed.Inform team members of completion of regulatory and contractual documents for individual sites.Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.Provide local expertise to SAMs and project team during initial and on-going project timeline planning.Perform quality control of documents provided by sites.May have direct contact with sponsors on specific initiatives.QualificationsBachelor’s Degree in life sciences or a related field and 3 years’ clinical research or other relevant experience; or equivalent combination of education, training and experience. In-depth knowledge of clinical systems, procedures, and corporate standards.Good negotiating and communication skills with ability to challenge, if applicable.Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.Knowledge of applicable regulatory requirements, including local regulations, , SOPs and company’s Corporate Standards.Understanding of regulated clinical trial environment and knowledge of drug development process.Ability to establish and maintain effective working relationships with coworkers, managers and clients.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 88.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dazu gehören integrierte Projektansätze entlang unseres IQVIA-Lösungsportfolios, die wir individuell an Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für einen bundesweiten Teamaufbau im Bereich Gynäkologie suchen wir zum 01.09.2026 mehrere Pharmaberater (m/w/d). Im Gebiet: Großraum Hamburg Rollenbeschreibung Verantwortung für definierte gynäkologische Zielkunden und Aufbau nachhaltiger KundenbeziehungenUmsetzung des Markteintritts im Bereich Women’s Health auf GebietsebenePositionierung des Produkts sowie Durchführung fundierter FachgesprächeAufbereitung und Präsentation klinischer StudiendatenEntwicklung und Umsetzung individueller Account-PläneSteuerung der Gebietsperformance unter Nutzung von CRM-Tools (z. B. Veeva)Enge Zusammenarbeit mit internen Schnittstellen unter Einhaltung von Compliance-Vorgaben​Erforderliche Qualifikationen Ein abgeschlossenes Studium in Naturwissenschaften oder eine vergleichbare Qualifikation nach §75 AMGGültiger Führerschein sowie Reisebereitschaft innerhalb des jeweiligen GebietsErfahrung oder Kontakte im Bereich Gynäkologie / Women’s Health bevorzugtSicherer Umgang mit Compliance-Vorgaben (inkl. SAMs)Ausgeprägte Kundenorientierung und überzeugendes AuftretenSensibilität und Offenheit im Umgang mit Women’s Health ThemenErfahrung mit CRM-Systemen (z. B. Veeva) von VorteilGute Englischkenntnisse von VorteilDas 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 KrankenzusatzversicherungenEin top ausgestatteter Firmenwagen mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des ModellsEine moderne IT-Ausstattung für Deinen modernen digitalen ArbeitsplatzUnser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige PerspektiveWir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines WohnortsVielfältige 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 BeschäftigungsverhältnissesUnser 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 #PharmaceuticalSales #PharmaRepresentative #Pharmacy #FieldSales #Gynäkologie#Woman’s Health 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. Komm in unser IQVIA-Team! Für ein spannendes Projekt im Bereich Impfstoffe suchen wir Pharmaberater (m/w/d) zum nächstmöglichen Zeitpunkt. Im Gebiet: Merseburg, Weißenfels, Naumburg, Zeitz, Querfurt, Bad Lauchstädt, Leuna   Das sind Deine Aufgaben: Durch die direkte Ansprache und intensive Betreuung ausgewählter Allgemeinmediziner, Internisten und Praktiker förderst Du die Verordnung Deines Impfstoff-Präparats und trägst so maßgeblich zum Unternehmenserfolg bei. In sehr eigenständiger Arbeitsweise bist du für den Aufbau und die Pflege langfristiger Beziehungen zu Ärzten und dem medizinischen Fachpersonal verantwortlich. Als Experte setzt Du auf der Basis Deines Fachwissens Beratungsstrategien erfolgreich um und überzeugst so Deine Ansprechpartner. Die Überwachung und das Management des Impfstoffbestands Deiner Kunden hast Du immer im Blick und stellst so eine kontinuierliche Verfügbarkeit und Versorgung sicher. Du erstellst eine eigenständige Routenplanung und pflegst Deine Besuche im CRM-System, inkl. Vor- und Nachbereitung. Das bringst Du mit: Du verfügst über eine naturwissenschaftliche Ausbildung (idealerweise Hochschulabschluss) oder Ausbildung zum Geprüften Pharmareferent (m/w/d) gemäß §75 AMG. Idealerweise verfügst Du über Erfahrung im Vertrieb von Impfstoffen bzw. hast eine hohe Bereitschaft und Begeisterung, Dich als Neueinsteiger in ein neues Aufgabengebiet einzuarbeiten. Als durchsetzungsstarke Persönlichkeit und erfahrener Netzwerker verstehst Du es, Dich und Deine Ansprechpartner zu begeistern. Du möchtest etwas bewegen – für Dein Präparat, für Dich selbst und vor allem für betroffene Patienten. Ausgeprägte kommunikative Fähigkeiten sowie die Bereitschaft, eigenverantwortlich und ergebnisorientiert zu arbeiten, runden Dein Profil ab. Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive. Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts. Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche. Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] #LI-CES #LI-DNP #LI-SS2 #Pharmaberater #Impfstoff #Chemie #Pharmareferent #75AMG #IQVIA #Pharma #Außendienst IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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 work with the preparation and documentation of clinical research projects in different therapeutic areas. We currently offer the exciting opportunity to join the team as Clinical Trials Assistant 2 (m/w/d) in full-time and work in a combination of office and home-office in the Düsseldorf area. Your responsibilities might include: Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for completeness. Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow. Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. Required knowledge, skills and experience: Bachelor’s or higher-level degree preferable in life science or High School Diploma and apprenticeship in life science, the medical or pharmaceutical field or office management. At least 2 years of experience as Clinical Trials Assistant or in another administrative role in clinical research, e.g. as Project Assistant, Study Coordinator, Study Nurse. Excellent knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Fluent languages skills in German on at least C1 level and good command of English. Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint. Effective communication, organizational and planning skills. Ability to work independently and to effectively prioritize tasks and to maintain effective working relationships with coworkers, managers and clients. Flexibility to visit our client's office in the Düsseldorf area on regular basis, about 2-3 days/week. Why join us? Permanent employment contract. Competitive compensation and benefits package. Flexible working schedules and combination of office and home-office. Ongoing learning and development. Whatever your career goals, we are here to ensure you get there! Please apply with your English CV, motivation letter and your certificates and reference letters. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewDirect and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources.  Essential Functions Oversee the execution of Site Activation (including pre-award/bid defense activities) and/or Maintenance for assigned projects in accordance with the agreed RSU site activation strategy, adhering to project timelines. Develop, implement and maintain the Management Plan according to the Scope of Work and Project Plan, within the agreed project strategy, resolving project related issues where required. Ensure collaboration across Regulatory & Site Activation, including communication with regions and countries, to successfully deliver the agreed project scope in compliance with the RSU Management Plan. Create and/or review technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Provide specialist regulatory and technical scientific support to facilitate efficient business development, initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Provide overall guidance and oversight of multi-regional and multi-protocol programs during initial start-up and maintenance phase as an integral member of the study management team. Determine regulatory strategy/expectations and parameters for submissions and all necessary authorizations Identify regulatory complexity and challenges and offer creative and practical solutions to support the bid process and subsequent execution of the site activation plan. Assess and review the regulatory landscape and contribute to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required. Execute operational strategy/ expectations for maintenance of clinical study approvals, authorizations and review/ negotiation of contracts and essential documents. Work with Quality Management to ensure appropriate quality standards for the duration of site activation (or Maintenance, as applicable). Mentor and coach colleagues as required. Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans with project specific information. May take a lead role in developing long standing relationships with preferred IQVIA customers. Deliver presentations/training to clients, colleagues and professional bodies, as required. May be involved in activities related to monthly study budget planning and reviews.  QualificationsBachelor's Degree Life sciences7 years’ relevant experience in a scientific or clinical environment including demonstrable experience in an international role. Strong negotiation and communication skills with ability to challenge Good regulatory and/or technical writing skills Strong knowledge and ability to apply Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines and applicable regulatory guidelines Good leadership skills, with ability to motivate, coach and mentor Excellent understanding of study financial management Proven ability to work on multiple projects balancing competing priorities In today’s world, continuing to grow and expand your skills is as important as ever. Discover career possibilities and chart your own path at IQVIA. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Join Our Team as a Therapeutic Strategy Lead!Are you passionate about creating innovative delivery strategies that meet customer needs? Do you thrive in a collaborative environment where you can make a real impact? If so, we have the perfect opportunity for you! Purpose As a Therapeutic Strategy Lead, you’ll develop and implement effective delivery strategies tailored to customer needs during the RFP/Bid Defense cycle. You’ll bridge the gap between sales, medical, and operational teams to ensure seamless project execution and support sales teams throughout the Business Development process. RESPONSIBILITIES Actively collaborate with Sales, Medical, Operations, and other functions and provide guidance to ensure tailor-made strategies to project or programs that differentiate IQVIA from the competition resulting in compelling, feasible proposals and continuously drive business growth.Scan the therapeutic and operational landscape and take account of wider impacts to develop long term implementation strategies that maximize opportunities to add value.Maintain an understanding of current and future market trends that may impact current and/or future innovative operational delivery strategies.Act as champion for project centricity within the organization through enabling the project delivery team assigned to an awarded project to understand and implement the project strategy that was sold.Drive the team to leverage and consolidate all available data to build the project strategy. Balance use of external research and data with IQVIA’s internal data sources.Guide and mentor assigned Project Leader so that they can confidently present the project strategy to the client and the internal stakeholders.Actively support Sales in the preparation and conduct of customer and bid defense meetings e.g. training and preparation of the assigned project team.Attend, present and lead or bid defense meeting or customer meeting, as requiredIdentify any quality issues within the study and provide coaching on resolution of issues, including implementation of corrective and preventative action plans and escalation.Ensure project/program budget(s) meet financial and company goals, including Gross New Business.REQUIRED KNOWLEDGE, SKILLS AND ABILITIES Deep and current knowledge of the scientific, clinical operations, real world, regulatory, operational, commercial and competitive landscape in applicable therapeutic area.·Strong global knowledge and awareness/understanding of the biopharma industry, drug development lifecycle and operational clinical trial delivery.In-depth knowledge of applicable clinical research regulatory requirements; e.g. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Strong business acumen including confidence with financial considerations, excellent negotiation and influencing skills, and comfort working in both sales and operational environments.Strong customer management skills and demonstrated ability to understand customer needs, have difficult conversations with internal/external stakeholders and customers, negotiate solutions and understand impacts on the overall program/portfolio.Strong leadership skills, ability to lead a virtual team in a matrix organization.Ability to work strategically to realize organizational and project goals, identifying and developing positive and compelling visions for the successful delivery of projects and taking account of a wide range of issues across, and related to, the projects and the organization.Strong presentation skills.Excellent written, verbal communication and interpersonal skills, including good command of English language (both written and spoken).Strong software and computer skills, including MS Office applications.Must have prior experience in the Clinical Research Organization (CRO) industryMINIMUM REQUIRED EDUCATION AND EXPERIENCE Bachelor's degree in life sciences and relevant global clinical research experience (director level), including hands on operational delivery and/or drug development experience in the applicable therapeutic area (Internal Medicine/Immunology)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.  #LI-remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Location – Region Southeast Netherlands In this role, you will lead the sales of clients’ products and services, driving growth in your territory by executing strategic plans and partnering with your line manager to deliver on key performance targets. Responsibilities Promote the company’s brands and manage product sales within your territory.Take ownership of your region by identifying innovative approaches, new business opportunities, customer needs, market trends, and competitor activities, and translate these into a relevant sales strategy in collaboration with your Line Manager.Develop and maintain a strategic business plan aligned with company standards and best practices, with guidance from your Line Manager.Execute the full range of sales activities, from introducing new products to delivering presentations and customer training, ensuring all stakeholders receive clear and consistent key messages.Act as a brand ambassador, representing the company at conferences, congresses, and trade fairs.Maintain accurate and up-to-date records in the CRM system in line with company standards.Collaborate closely with the Marketing and Medical teams to achieve shared goals.Knowledge & skills required Strong knowledge of the assigned territoryGood understanding of key stakeholders in the healthcare sector, particularly in wound and skin care in The NetherlandsStrong customer focus and entrepreneurial mindsetResults-driven, with a high level of comfort working with numbers and market analysisExcellent verbal and written communication skillsStrong presentation and negotiation skillsProficient in Microsoft Office, CRM systems, and ShowpadValid driving licenseExperience required Previous experience in field sales within a medical environment Education Higher professional education (HBO) in a commercial or medical field, or equivalent through relevant experience Languages Native-level Dutch and fluent in English, both written and spoken Please note you must have the right to work in the EU. This role does not sponsor visa's.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 88.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dazu gehören integrierte Projektansätze entlang unseres IQVIA-Lösungsportfolios, die wir individuell an Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für einen bundesweiten Teamaufbau im Bereich Gynäkologie suchen wir zum 01.09.2026 mehrere Pharmaberater (m/w/d). Im Gebiet: Großraum Düsseldorf /Ruhrgebiet Rollenbeschreibung Verantwortung für definierte gynäkologische Zielkunden und Aufbau nachhaltiger KundenbeziehungenUmsetzung des Markteintritts im Bereich Women’s Health auf GebietsebenePositionierung des Produkts sowie Durchführung fundierter FachgesprächeAufbereitung und Präsentation klinischer StudiendatenEntwicklung und Umsetzung individueller Account-PläneSteuerung der Gebietsperformance unter Nutzung von CRM-Tools (z. B. Veeva)Enge Zusammenarbeit mit internen Schnittstellen unter Einhaltung von Compliance-Vorgaben​Erforderliche Qualifikationen Ein abgeschlossenes Studium in Naturwissenschaften oder eine vergleichbare Qualifikation nach §75 AMGGültiger Führerschein sowie Reisebereitschaft innerhalb des jeweiligen GebietsErfahrung oder Kontakte im Bereich Gynäkologie / Women’s Health bevorzugtSicherer Umgang mit Compliance-Vorgaben (inkl. SAMs)Ausgeprägte Kundenorientierung und überzeugendes AuftretenSensibilität und Offenheit im Umgang mit Women’s Health ThemenErfahrung mit CRM-Systemen (z. B. Veeva) von VorteilGute Englischkenntnisse von VorteilDas 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 KrankenzusatzversicherungenEin top ausgestatteter Firmenwagen mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des ModellsEine moderne IT-Ausstattung für Deinen modernen digitalen ArbeitsplatzUnser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige PerspektiveWir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines WohnortsVielfältige 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 BeschäftigungsverhältnissesUnser 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 #PharmaceuticalSales #PharmaRepresentative #Pharmacy #FieldSales #Gynäkologie#Woman’s Health 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 Director, Business Transformation (AI Transformation) leads the definition, articulation, and execution of the enterprise AI transformation strategy, ensuring it is clearly understood, consistently applied, and translated into measurable business outcomes. This role is accountable for establishing the strategic narrative, transformation framework, and operating model that connect vision to execution - enabling scalable, repeatable adoption of AI across core business processes.Key Responsibilities•    Support the development of the AI transformation strategy, ensuring alignment with enterprise priorities•    Translate strategy into a clear, compelling narrative for leaders and teams•    Drive consistent communication of “what, why, and how” across the organization•    Partner with executives to ensure alignment, clarity, and sponsorship•    Act as a strategic advisor to senior leaders on AI transformation priorities•    Drive cross-functional alignment across Business, IT, Data, and Product teams•    Build organizational capability in AI-enabled transformation and strategic execution•    Coach teams on structured problem solving and strategy-to-execution disciplineKey Deliverables•    Clear, enterprise-wide AI transformation strategy and narrative•    Standardized transformation framework and methodology•    Executive communication and reporting materialsExperience & Qualifications•    10+ years in business transformation, strategy, or consulting•    Proven ability to define and communicate strategy at an executive level•    Experience leading enterprise transformation programs•    Strong understanding of AI/automation and business application•    Track record of bridging strategy to execution and delivering results 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 $108,100.00 - $300,800.00. 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.