IQVIA

Perform comprehensive data management tasks including data review, query generation and query resolution. This may also include, but is not limited to creation of eCRF completion guidelines, entry of test data for eCRF and the Data Review Model, testing of data validation rules, etc. Data Management tasks should be inclusive of Study Start-up, Execution, Database Lock and Close-out.Perform ongoing Data Reconciliation of all data streamsAttend study related meetings/teleconferencesPerform Study Closeout/Archiving Activities including QC of subject/site archival CRFsCreate and provide status/metric reportsGenerate reports on EDC and track cleaning progressManage Freeze / lock of eCRFFile documentation in the virtual Trial Master File (TMF)Receives and enters lab normal rangesIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewProvide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager. Essential Functions• Serve as a Data Operations Coordinator (DOC) for one protocol with less then 5 operations staff (excludes DE) or 15+ easy to moderately complex central laboratory studies, or serve in a leadership role in a specific data management task (e.g., coder, tester or database designer for technologies that don't require extensive programming expertise) with guidance.• May serve in the role of back-up to a DOC or DTL.• May conduct data review.• May write and resolve data clarifications.• May lead database audit team.• May develop and test databases and edit specifications.• May perform testing of programming.• May perform clinical data coding. Understand and comply with core operating procedures and working instructions. Meet objectives as assigned. Develop and maintain good communications and working relationships with CDM team." Qualifications• Bachelor's Degree Clinical, biological or mathematical sciences, or related field Req• Equivalent combination of education, training and experience in lieu of degree.• Medical terminology exposure. Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Medical terminology exposure. Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. 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 OverviewManage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team to provide high quality data management products that meet customer needs. Provide leadership to the team in the areas of project planning, execution, and close-out; Overview of financial management for data management activities; communications; and milestone deliverables. Perform role of Data Team Lead (DTL).  Essential Functions• Gather Study Set up requirements through discussion and communication with relevant stakeholders.• With Minimal guidance - support, overview of validation of new Device integrations.• Oversight & Perform regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor.• Ensure that all the deliverables are of expected quality standards and meet customer expectations.• With guidance, ensure service and quality meet agreed upon timelines and deliverables in contract/Scope of Work (SOW).• Support Training of New joiners.• Lead internal study meetings and internal/ sponsor audits and participate in Study Kick off meetings and other sponsor meetings.• Tracks and manages the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended as required.• With Guidance manage & oversight the implementation of new technology / database revisions.• Work closely with the programming team for process innovation and automation.• Be compliant to trainings and eSOP reading.• Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions.• Communication with Line Manager, and other team members across functions should be collaborative.• Perform other duties as directed by Line Manager. Qualifications• Bachelor's Degree In health, clinical, biological or mathematical sciences, or related field with proven experience in Data Management Req• 3 -4 years direct Data Management experience, including a minimum of 1 year as a CDM project lead. Pref• English Fluency Spoken and English Advanced• Advanced computer applications like Microsoft excel, word, Inbox etc Advanced• Should have Advanced understanding of Drug development lifecycle and Overall Clinical research process Advanced 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 OverviewAs a Senior Data Platforms SRE, you will serve as a technical escalation point and resolve higher complexity incidents and technical problems end to end. This role requires advanced troubleshooting expertise in data platforms, operational discipline, and the ability to drive service improvements across the governance team. You will work directly with Databricks and Snowflake platforms deployed on Azure and AWS, investigating non-trivial technical issues, implementing platform guardrails, and mentoring junior engineers to elevate the team's operational maturity. The position combines hands-on technical work with service improvement initiatives, including defining operational metrics, tracking incident resolution trends, and contributing to SLA/SLO verification to ensure platform reliability and cost effectiveness. Level 2 support engineers handle technically complicated issues that exceed the competence of Level 1 support, focusing on incident resolution through deep technical knowledge and advanced troubleshooting skill.Key ResponsibilitiesAdvanced Incident Handling & Escalation: Investigate non-trivial job and pipeline failures, performance and capacity symptoms, and recurring platform issues. Coordinate escalation to platform engineering or vendors with complete diagnostics, including root cause analysis, system logs, and performance metrics to ensure rapid resolution. L2 engineers perform deep diagnoses to trace and resolve issues, managing support tickets to ensure timely resolution of all technical incidents .Resource & Cost Governance: Perform spend anomaly checks to identify runaway queries, oversized clusters, and job loops that drive uncontrolled costs. Drive remediation actions including shutdowns and guardrails using policy and operational authority, ensuring alignment with financial controls and budget targets.Platform Guardrails Implementation: Implement and maintain cluster policies and operational restrictions that prevent uncontrolled cost growth, aligned with governance objectives. Configure and enforce workspace-level controls, quota management, and resource limits across Databricks and Snowflake environments.Environment Lifecycle Execution: Support workspace and environment provisioning and decommissioning activities, including Infrastructure as Code driven provisioning where defined. Execute environment setup, configuration validation, and teardown procedures following established operational standards.Service Improvement & Metrics: Help define and track operational metrics including incident volumes, resolution trends, and mean time to resolution. Contribute to SLA/SLO verification and improve documentation quality and consistency across the service to support continuous operational improvement. L2 support engineers maintain detailed documentation and knowledge articles as key activities in their role.Mentoring & Coaching: Mentor junior engineers on troubleshooting methodologies, ticket handling best practices, and technical documentation standards. Review tickets for completeness, ensure clean handoffs between support tiers, and raise the overall operational maturity of the team through knowledge sharing and skills development. 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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is looking for a driven and analytically rigorous Business Analyst to join our Commercial Effectiveness Services (CES) team, based in Algiers You will play a central role in the design and delivery of data-driven commercial solutions for pharmaceutical and life sciences clients across North, East, and West Africa. What You'll Work On Customer targeting and segmentation (HCP and pharmacy)Sales force structuring, sizing, and territory alignmentIncentive and target-setting modelingPerformance dashboarding and KPI trackingMarket and competitive analysis to support client decision-makingMain Responsibilities Collect, clean, and structure large datasets from multiple sources to build analysis-ready modelsConduct end-to-end quantitative analysis — from raw data processing through to synthesis, interpretation, and business recommendationsBuild and maintain Excel models, Power BI dashboards, and structured PowerPoint deliverables for client presentationsContribute to the delivery of multiple simultaneous client engagements across the Africa regionSupport project proposals and client interactions under senior supervisionRequired Profile Strong analytical and critical thinking skills — comfortable with ambiguity and able to translate data into actionable insightsSolid command of Excel (advanced formulas, pivot tables, modeling) and PowerPointMaster's degree in Economics, Statistics, Mathematics, Computer Science, or equivalentProficiency in English (French and/or Arabic are strong assets for the Africa region)0–3 years of experience in consulting, analytics, or a pharmaceutical/healthcare environmentNice to Have Experience with Power BI or equivalent BI toolsSQL skillsExposure to pharmaceutical commercial data (IMS/IQVIA syndicated data, CRM outputs)IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Clinical Research Coordinator - Albuquerque, NMWork Set‑Up: On‑siteSchedule: 24 Hours/Week (Part‑time)About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We collaborate with leading pharmaceutical, biotechnology, and medical device organizations to advance innovation and improve patient outcomes worldwide. Through scientific expertise, operational excellence, and cutting‑edge technology, IQVIA is shaping the future of healthcare. About the Role IQVIA is seeking a Clinical Research Coordinator (CRC) to support clinical research studies conducted under the supervision of a Principal Investigator. This role is well‑suited for a detail‑oriented research professional who enjoys direct patient interaction, values data integrity, and is committed to high‑quality clinical research within diverse communities. As a CRC, you will play a critical role in coordinating study operations, supporting patient recruitment and retention, performing study‑related procedures, and ensuring adherence to study protocols and regulatory requirements. Key Responsibilities Coordinate and conduct clinical research activities in accordance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements Perform study‑related clinical procedures, including ECGs, vital signs, and biological sample collection Conduct patient visits including screening, enrollment, education, orientation, and follow‑up Support patient recruitment efforts and community outreach, including bilingual (English/Spanish) communication Prepare study materials, manage equipment setup, and support daily clinic operations Accurately collect, document, and enter clinical data into electronic data capture (EDC) systems and case report forms (CRFs) Request, review, and manage medical records to support study eligibility and documentation Collaborate with investigators, sponsors, and monitors to address data queries and ensure study quality Maintain a safe clinical environment and serve as a patient advocate throughout study participation Qualifications Bachelor’s degree preferred, or an equivalent combination of education and relevant experience Minimum of 1+ year of clinical research coordination experience, including prior study coordination Hands‑on experience with clinical research operations, including: Data entry and query resolution in EDC systems Chart pre‑screening and patient pre‑screening activities Conducting and coordinating patient visits Patient outreach and education via phone and face‑to‑face communication regarding clinical trials Scheduling study visits and managing visit logistics Collection, processing, and shipping of laboratory samples Recruitment activities and participant follow‑up Regulatory document review and maintenance Working knowledge of clinical trial processes, GCP guidelines, and medical terminology Experience requesting and managing medical records Bilingual in English and Spanish (written and verbal) is preferred but not required Strong organizational skills, attention to detail, and ability to work effectively with diverse teams and patient populations Ready to Make an Impact? Join IQVIA and contribute to high‑quality clinical research that advances science while serving diverse patient communities.Apply today and be part of a team helping bring innovative treatments to patients. Additional Information This position is not eligible for visa sponsorship #LI-CES #LI-DNP #LI-HCP #ONSITE IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job OverviewProvide advanced technical expertise to develop and maintain programs to meet internal and external clients’ needs.  Plan and lead the development of project-related solutions to the full scope of statistical programming tasks.  Provide technical expertise to the Statistical Programming department. Essential Functions• Perform and plan: (i) the programming, testing, and documentation of programs for use in creating statistical tables, figures and listing summaries, (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and plan the programming of database quality control checks.• Program the integration of databases from multiple studies or sources.• Develop programming documentation including plans and specifications, as appropriate.• Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and department.• Perform and plan the development, implementation and validation of new process technologies, macros and applications.• Fulfill project responsibilities at the level of statistical team lead for single studies, under supervision.• Understand the Scope of Work, estimate the work completed, and manage Out of Scope for single studies. May manage budget and resource requirements and provide revenue and resource forecasts for single studies. May be required to understand budget and quote assumptions.• Provide training and guidance to lower level and new staff. Qualifications• Master's Degree Computer science or related field and 5 year relevant experience Req Or• Bachelor's Degree Computer science or related field and 5 years relevant experience Req• Equivalent combination of education, training and experience Req• Knowledge of statistics, programming and/or clinical drug development process• Working knowledge of computing applications such as Base SAS, SAS/STAT and SAS Macro Language• Good organizational, interpersonal, leadership and communication skills• Ability to effectively handle multiple tasks and projects• Excellent accuracy and attention to detail• 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.

Ervaring als medisch afgevaardigde op zak en zin om verder te bouwen? In deze rol krijg je autonomie en de kans om je talenten volop te ontwikkelen in het veld. Wat houdt de job in? Promotie van het Sandoz‑portfolio bij huisartsen, specialisten en apothekers.Analyseren van markt- en businessdata om sterke strategieën en actieplannen op te bouwen.Verhogen van salesperformantie, marktaandeel en klanttevredenheid binnen jouw regio.Inspelen op de noden van klanten en aanbieden van passende oplossingen.Opbouwen van duurzame professionele relaties met HCP’s binnen verschillende therapeutische domeinen.Trends uit het veld detecteren en waardevolle inzichten delen met het management.Actieve deelname aan educatieve en wetenschappelijke events voor zorgprofessionals.Wat breng jij mee? Een Bachelor in Farmaceutische Wetenschappen, (Bio)wetenschappen, Business of een gelijkwaardige richting.3–5 jaar ervaring in sales, bij voorkeur in de farmaceutische sector.Vlotte digitale vaardigheden en ervaring met CRM‑systemen.Sterke communicatieve skills in het Nederlands en Engels.Ondernemerschap, flexibiliteit en een echte go‑getter mentaliteit.Commerciële vaardigheden zoals onderhandelen, accountmanagement en analytisch inzicht.Teamspirit en de drive om bij te dragen aan een positieve bedrijfscultuur.Wat hebben we jou te bieden? Contract onbepaalde duur met mogelijkheid tot integratie bij de klant.Competitief salaris afgestemd op jouw ervaring.Aantrekkelijk pakket aan extralegale voorwaarden (inclusief bedrijfswagen + laadkaart, groeps- en hospitalisatieverzekering, ..).Uitdagende functie met veel autonomie.Begeleiding en opleiding.Klaar om impact te maken? Solliciteer nu! Of stuur je cv naar [email protected] #LI-MB1 #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.

V Voor een opportuniteit bij één van onze klanten zoekt IQVIA een ervaren, gedreven farmaceutisch afgevaardigde. Je komt terecht bij een internationale farmaceutische speler , actief in de ontwikkeling en commercialisering van kwalitatieve geneesmiddelen. Wat houdt de job in? Bezoeken van zelfstandige apotheken en apotheekgroeperingen binnen jouw regioPromoten en positioneren van een sterk portfolio met focus op OTC‑productenOpbouwen en onderhouden van duurzame relaties met apothekers en hun teamsWat breng jij mee? Je hebt ervaring met het promoten van OTC productenJe bent matuur, verantwoordelijk en werkt zelfstandigJe wil echt mee het verschil makenJe bent proactief, ondernemend en neemt graag initiatiefJe hebt een commerciële mentaliteit en denkt graag strategisch meeJe communiceert vlot in NederlandsWat hebben we jou te bieden? Een competitief salaris, afgestemd op jouw ervaringEen aantrekkelijk pakket aan extralegale voordelen,Een uitdagende functie met veel autonomie binnen een groeiende en stabiele omgevingGrondige begeleiding en opleiding, zodat je sterk van start kan gaan en je verder kan ontwikkelenRegio: Edegem , Wilrijk, Puurs, Asse, Halle, Dilbeek, Aalst, Aalst Arr, Dendermonde, Beveren, Ninove Klaar om impact te maken? Solliciteer nu! #LI-MB1 #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.

Combineer je medische kennis en communicatieve skills als jr. medisch afgevaardigde en bouw sterke vertrouwensrelaties op met artsen in regio Antwerpen, Edegem, Wilrijk, Mortsel, Putte, Lier Wat houdt de job in? Klantenopvolging Huisartsen en specialisten bezoeken en een professionele vertrouwensrelatie met hen uitbouwenDe wetenschappelijke kennis assimileren en ze op een gestructureerde, duidelijke en overtuigende manier overbrengenAnalyse, planning Actieplannen opstellen om de vooropgestelde objectieven te bereikenDe feedback van je dokters verwerken en analyserenDeelnemen aan meetings (team meetings, seminaries, cycle meetings)De belangrijkste artsen in je doelgroep identificerenWat breng jij mee? Je beschikt over een Bachelor of Master diploma (in een wetenschappelijke of commerciële richting)Je bent positief ingesteld, enthousiast, leergierig, ondernemend, klantgericht en flexibel.Je beschikt over uitstekende communicatieve vaardigheden en staat open voor verandering.Je bent sales gedreven.Je beschikt over een rijbewijs B en woont in de regioWat hebben we jou te bieden? Contract onbepaalde duurCompetitief salaris afgestemd op jouw ervaringAantrekkelijk pakket aan extralegale voorwaarden (inclusief bedrijfswagen + laadkaart, groeps- en hospitalisatieverzekering, ..)Uitdagende functie met veel autonomieBegeleiding en opleiding#LI-MB1 #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.

We are seeking Associate Laboratory Project Services Manager to join IQVIA Laboratories at Valencia, CA.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:Manage laboratory aspects of assigned clinical trial projects from start-up through closeout while serving as a key client contact throughout the study lifecycle. In this role, you will help ensure quality deliverables are completed on time and within budget while supporting strong collaboration across cross-functional teams. What You'll Be Doing:Manage assigned clinical trial projects across start-up, maintenance, and closeout activitiesReview study protocols, budgets, and project requirements to support effective study planning and set-upLead client communications and serve as the primary point of contact for study-related laboratory servicesMonitor timelines, deliverables, study scope, budgets, change orders, and project risksCoordinate cross-functional teams to resolve issues, support milestones, and maintain service qualityOversee protocol-specific laboratory documentation, instructional materials, and study plansReport study progress to internal and external stakeholders and drive proactive problem resolution What We Are Looking For:Bachelor's Degree in Life Sciences and/or related field preferredTypically requires 2 - 3 years of prior relevant experienceWorking knowledge of project management processes and central laboratory operations, including kits and supplies, logistics, specimen storage, data reporting and transfers, and site alerts preferredDemonstrated computer proficiency with Microsoft Office and company systems, or equivalent experience with similar centralized laboratory systems preferredOther 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 client management skills with the ability to build effective working relationships with coworkers, managers, and clientsStrong written and verbal communication skills, including good command of English languageDemonstrated ability to work in a fast-paced environment while maintaining organization, composure under pressure, and meeting deadlinesWorking understanding of medical and clinical research terminologyExperience leading problem solving and resolution efforts in a timely, client-focused manner 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 $62,000.00 - $129,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

We are seeking an Associate Manager, Flow Cytometry to join IQVIA Laboratories on site at Valencia. 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. As an Associate Manager, Flow Cytometry, you will lead daily laboratory operations, supervise a team of scientists, and ensure high‑quality, compliant delivery of flow cytometry testing. What You’ll Be DoingLead and supervise a team of laboratory staff to ensure accurate and timely operational delivery. Oversee daily workflow, assign tasks, and resolve technical or workload challenges. Hire, train, mentor, and evaluate staff performance under the guidance of senior management. Monitor reagent and supply inventory, ensuring availability and adherence to budget. Ensure compliance with safety, quality, CAP/CLIA, and regulatory requirements. Review laboratory metrics to identify process improvement opportunities and drive efficiency initiatives. Partner with cross‑functional stakeholders to implement new tests, equipment, and procedures. Serve as a backup for daily laboratory operations as needed. What We Are Looking ForBachelor’s degree in a chemical, physical, biological, or clinical laboratory science, medical laboratory technology, or related field. Minimum 4 years of experience in a regulated laboratory environment, including at least 2 years in flow cytometry. Demonstrated experience supervising, training, or mentoring laboratory staff. Strong technical background in laboratory operations, including hands‑on skills such as pipetting and assay execution. Other equivalent combinations of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This RoleIn‑depth knowledge of flow cytometry, clinical testing procedures, quality control, and laboratory regulations (CAP/CLIA). Strong leadership, communication, and problem‑solving skills with the ability to manage multiple priorities. Working knowledge of quality assurance, safety standards, root‑cause analysis, and CAPA processes. Ability to collaborate across teams, drive process improvements, and maintain a high‑performance laboratory environment. What We Offer YouWe 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. 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 $58,800.00 - $122,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job Location: Calicut Job OverviewMaximize sales growth in a specified geographical territory, consistent with Company strategy and objectives. This is generally achieved by educating and informing physicians and/or hospital staff on the features and benefits the customer’s product(s) versus competitor products in order to increase prescriptions and/or use by the healthcare professionals. Essential Functions• Achieve assigned activity goals and targets for the territory as agreed with the reporting manager, with an initial high level of supervision and coaching provided by the company, customer and manager.• Conduct sales interviews, carry out pre-call planning and preparation and develop a self analytical approach in order to identify learning areas from each call.• Promote and sell customer’s therapeutic products to general practitioners, other identified healthcare providers, and/ or other healthcare professionals in the retail market.• Within a specific geographical territory, identify target customers while maintaining and analyzing customer records.• Maintain records in the reporting systems within the required timescales.• Effectively utilize the relevant software (e.g. Electronic Territory Management System, CRM systems) to maintain records updated and to report daily calls.• Organize and hold group events to optimize business while complying with relevant country legislation.• Keep Line Manager informed about changes in competitor activities and other market changes.• Maintain an up-to-date sales / technical knowledge of specialty and disease areas and relevant publications as per customer profile.• Keep all Company equipment safe and in a good state of repair.• Share experiences, ideas and techniques in order to assist with the sales training of colleagues.• Discuss, agree and document assigned activity, Key Performance Indicator tools, and targets as agreed with Line Manager.• Successfully complete career development courses and additional training as required by the customer.• Ensure the reporting of any identified Adverse Events in line with prevailing process and guidelines.• Project a professional impression of the Company and act in accordance with the relevant Pharmaceutical Industry’s Code of Practice• Perform other duties as assigned. Qualifications• High School Diploma or equivalent 5 years’ relevant experience Req Or• Bachelor's Degree Life Sciences or related field Req• Equivalent combination of education, training and experience may be accepted in lieu of educational requirements Req• Basic knowledge of Pharma Market and related procedures.• Fluency software operating systems, such as MS Office and customer relationship management systems.• Effective verbal and written communication skills.• Ability to conduct face to face presentations to customers.• Ability to prioritize and coordinate multiple work requirements to meet deadlines.• Ability to establish and maintain effective working relationships with co-workers, managers and clients.•  Make plans to obtain any industry qualifications essential to function as a Medical Representative in the relevant market.  Req• AZDL  - Driver Licence - Valid And In State   Req IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Role Purpose: Responsible for the daily maintenance of healthcare Organizations and Prescribers in all database of the US Region. Validates, research & analyses to client data inquiries with the use of the process tool. Job Responsibilities: Complete maintenance of reference data (healthcare Organizations and Prescribers) as essential for US Production. Perform research such as Internet Search, Phone Verification, Database Matches and etc. to gather information from third parties that will validate the completeness or accuracy of the data. Perform outbound phone verification of details on Organization and Prescriber records to validate accuracy of reference data maintained as well as capture client-required details such as primary office address and primary profession/specialty. Performs ad hoc data analysis and participates on various process improvement as needed. Validate that the information gathered from third-party sources represents accurate new data that should result in an update, creation, or deletion in the database existing data. Job Requirement: High School Diploma or equivalent Req Experience in handling voice and healthcare account is an advantage but not a requirement. Basic knowledge in Windows applications (Excel, Word). Strong verbal and / or written communication skills in either the language of the country supplied or English. Critical thinking and problem-solving skills. Demonstrate strong understanding of complex concepts and processes.  Has initiative and is self-motivated to see through until resolution concerns raised by Clients. Candidate must be willing to work in night. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Description Summary: Under appropriate guidance, ensure that personal administration and HR processes are executed in-country in full compliance with local labor legislation, Core HR standards, and corporate policies. The role is offered as a two-year maternity cover. Core Responsibilities: •    With limited guidance, deliver comprehensive HR support to employees and managers across assigned service areas, business units, or functions.•    Independently manage HR-related inquiries and collaborate with senior HR team members and line management as required to address complex issues.•    Manage employees in accordance with organizational policies and applicable employment laws, including responsibilities related to hiring, terminations, and employee relations matters.•    Build and maintain strong, effective working relationships with HR specialist functions and Centers of Excellence, including HR Shared Services Tier 1, HR Business Partners, Payroll, and Benefits teams.•    Support line managers, as appropriate, in the delivery of new employee orientation and onboarding activities.•    Conduct ad hoc reviews as directed and provide recommendations on employment legislation, compliance, HR systems, practices, and procedures; support and educate line management with appropriate guidance.•    Partner with senior HR team members on organizational effectiveness and change management initiatives related to reorganizations, mergers and acquisitions, and employee transfers, ensuring compliance with local legislation.•    Participate, with minimal supervision, in the day-to-day development and implementation of local and global HR initiatives, including redesign and transformation efforts.•    Prepare and deliver HR reports and analyses as requested by senior management.•    Actively contribute to continuous improvement initiatives to enhance service quality, exceed customer expectations, and promote a professional HR organization.•    Scope of responsibility: Bulgaria Qualifications: •    Bachelor’s degree required.•    Fluency in Bulgarian language is required, with proficiency in English.•    1-2 years of experience in an HR function or in personnel administration processes; prior experience in an HR Shared Services environment is an added advantage.•    Proficiency in Microsoft Office applications; experience with Workday and DocuSign is considered an advantage.•    Demonstrated ability to exercise sound judgment within established procedures and practices to determine appropriate actions.•    Proven ability to prioritize and coordinate multiple work requirements to meet deadlines effectively.•    Ability to establish and maintain effective working relationships with colleagues, managers, and internal clients.•    Strong knowledge of local and relevant employment legislation.•    Excellent verbal and written communication skills, with strong interpersonal capabilities.•    Ability to work effectively both independently and as part of a team.•    Strong attention to detail and the ability to operate successfully within a matrixed organizational environment. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Essential Functions• 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. Qualifications• Bachelor's Degree Related field• 1 year clinical research experience. Equivalent combination of education, training and experience.• In-depth knowledge of clinical systems, procedures, and corporate standards• Strong knowledge of medical terminology and regulations• Broad knowledge of clinical research• Strong knowledge of Microsoft Office and e-mail applications• Effective communication, organizational, and interpersonal skills• Ability to work independently and to effectively prioritize tasks• Ability to manage multiple projects• Attention to detail• 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 OverviewManages multiple consulting projects of varying complexity and ensures on-time and on-budget delivery for clients in the life sciences field. Contributes to new business development and maintaining and strengthening client base. May support the development of new offerings. Essential Functions• Manages project teams including both internal and external resources in the design, development and delivery of client solutions.• Leads teams to review and analyze client requirements or challenges and develops and costs associated proposals that ensure profitability and high client satisfaction with limited if any senior management input.• Manages the process of proposal preparation and/or modifications including overall bid integrity.• Develops project plan with timelines and deliverables and leads project to successful completion, on-time and on-budget, from start to finish with limited senior management guidance.• Recommends improvements and alternative solutions to resolve problems.• Serves as key point of contact with client.• Provides high level input to, and ensures the development of, client reports and presentations and delivers all or significant portions of findings to client.• Develops and/or elevates new business opportunities through the identification of follow-on work and new leads.• Provides follow-up with client after project deliverable have been completed to ensure client satisfaction.• Proactively continues to strengthen subject matter expertise through on the job experience, participation in conferences and symposiums and other forums for professional knowledge sharing.• Proactively mentors, coaches and shares subject matter expertise with others to elevate our capabilities to deliver world-class solutions for clients. Qualifications• 10+ years of related experience including consulting and/or life sciences industry experience• Experience in strategic consulting and/or Go-to-Market (GTM) strategies • Demonstrates excellent project management skills and client influencing and relationship building skills.• In-depth understanding of IQVIA data assets and the IQVIA core offerings.• Works willingly and effectively with others in and across the organization to accomplish team goals.• Experienced with developing consultative relationships with senior level managers and executives at clients in the life sciences industry.• Ability to manage multiple projects, juggle priorities and deliver on tight deadlines.• Knowledge of consulting methodologies, tools and techniques related to functional area.• Knowledge of key issues and current developments in the life sciences industry.• Excellent presentation, communication and client influencing skills.• Has established network and referral contacts.• Possesses the necessary subject matter expertise and project management skills able to effectively manage projects across more than one CoE. [추천 컨텐츠]1. What does it mean to be IQVIAN? (Video)2. 아이큐비아ㅣ나만 몰랐던 (진짜) 포브스 선정 '세계 최고의 직장'  (Video)3. 한국아이큐비아 : 네이버 블로그 (Blog) [관련 문의]한국 아이큐비아 채용(IQVIA) 카카오톡 채널을 통해 1:1 문의 하실 수 있습니다.*채널을 추가하시면 매월 신규 포지션 알림 및 회사 소식을 받아보실 수 있습니다. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Overview• Provide high quality, on-time input to market research projects in the healthcare field, with limited support/guidance from senior member/project leader.• Assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex solutions. Essential Functions• Support overall execution of market research project to ensure timely delivery and the development of proposals• Assist in drafting research materials and other tasks leading up to final report preparation (qualification for either quantitative and qualitative studies as below requirements are acceptable):- Quantitative studies: Questionnaire design, table specs, code frames, report charting with error-free, writing key takeaway messages, etc.- Qualitative studies: drafting discussion guide, conduct in-depth interviews with necessary supervision from project leader, prepare content analysis/ summary of IDIs, assist in qualitative report preparation, etc.• Proactively develops a market research methodology/industry knowledge through the delivery of market research engagements and participation in formal and informal learning opportunities• Well time/resource management when handling multi-studies.• Keep effective performance & well EQ management under pressure. Qualifications• More than 3 years of experience in Market Research (preferred Healthcare & Pharma exp.) (Position level will be aligned with the candidate’s experience.)• Experience in marketing/Product Manager roles in Pharmaceutical companies is also preferred.• Mainly act as a project delivery lead. [추천 컨텐츠]1. What does it mean to be IQVIAN? (video)2. 아이큐비아ㅣ나만 몰랐던 (진짜) 포브스 선정 '세계 최고의 직장' (video)3. [아이큐비아 직업탐구] 정확한 제약시장 분석을 위한 Primary Intelligence (article) [관련 문의]한국 아이큐비아 채용(IQVIA) 카카오톡 채널을 통해 1:1 문의 하실 수 있습니다.*채널을 추가하시면 매월 신규 포지션 알림 및 회사 소식을 받아보실 수 있습니다. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.• Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.• Assist with periodic review of study files for completeness.• Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.• May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.• May collaborate with the clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Qualifications• A minimum of 1 year of experience in a CTA role is required.• Strong communication skills in English (both spoken and written) are essential.• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.• Written and verbal communication skills including good command of English language.• Effective time management and organizational skills.• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.• Basic knowledge of applicable clinical research regulatory requirement, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.• Knowledge of applicable protocol requirements as provided in company training. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Visão Geral:O aprendiz irá suportar as rotinas administrativas dos projetos do setor de Pesquisa Clínica (Regulatório), auxiliando principalmente com organização de documentos tecnicos, atualização de dados em sistema e suporte na comunicação com os centros de pesquisa para validação de status. Descrição das atividades: Organização de documentos e planilhas; Apoio na preparação de pacotes éticos e regulatórios (CEP, CONEP, ANVISA), no início de estudo e na etapa de manutenção; Suporte nas atividades de ativação de centros de pesquisa e na manutenção do estudo, negociação de contratos, emendas de contrato e orçamentos com centros de pesquisa e importação; Acompanhamento de atividades e preenchimento de sistemas internos; Apoio em comunicações com times internos e centros de pesquisa.  Requisitos: Ensino médio cursando, completo ou cursando técnico/profissionalizante (dentro dos critérios para o programa de aprendizagem); Conhecimento do pacote Office (Word, Excel, Outlook); Inglês intermediário (para se comunicar com alguns materiais e realizar interações internas); Disponibilidade para atuar em modelo híbrido no escritório em São Paulo/SP. A IQVIA está empenhada em adotar um ambiente de trabalho diverso e inclusivo. Nosso objetivo é atrair e reter as melhores pessoas, independentemente de gênero, raça, estado civil, origem étnica, nacionalidade, idade, deficiência, orientação sexual, identidade de gênero ou qualquer outra característica. Junte-se a nós! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Clinical Trial Manager – Sponsor Dedicated.   Clinical Trial Management services provide management of a clinical trial (s) in a local level. Services/deliverables include operational oversight of assigned project(s) at the local level for end-to-end project management from start-up through to closeout activities.   Tasks & Responsibilities:   • Services rendered will adhere to applicable Sponsor SOPs, WIs, policies, codes of Good Clinical Practice (GCP), local regulatory requirements. • Prepares or contributes to high level budget estimate in response to Request for Service’s followed by detailed budget proposal. Ensures overall contract management, including review and approval of external service provider (ESP) contracts, change orders and ensures services are delivered per contract. • Act as primary company contact for assigned trial at the country level and ensures local/country team is tracking project progress against planned timelines and monitors patient recruitment rate to ensure that target enrollment will be met across the allocated countries. This may require development of local trial specific procedures and tools, recruitment planning, contingency and risk management, and budget forecasting. • Drive study compliance by maintaining and updating trial management systems, using study tools and management reports available to analyze trial progress. Participates in preparation for and conduct of Health Authority (HA) inspections and internal Quality Assurance audits. Escalates corrective and preventive actions (CAPA) to GTL MAO and CPL when the trial deviates from plans and communicates study progress and issues to study management teams and business partners. • Contributes to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target. • Contributes to patient understanding of protocol and patient safety by contributing to the review of country specific informed consent in accordance with procedural document/templates. This includes reviewing and managing site specific informed consent forms in accordance with SOPs, other procedural documents and applicable regulations.     Essentials Requirements:   • BA/BS degree. • Degree in a health or science related field. • Minimum of 1 years of local/regional trial management experience in the pharmaceutical industry or CRO and previous experience as Clinical Research Associate. • Specific therapeutic area experience in cardiology is required. • Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures. • Strong IT skills in appropriate software and company systems. Willingness to travel with occasional overnight stay away from home according to business needs. • Excellent decision-making and string financial management skills. • Proficient in speaking and writing the country language and English. Good written and oral communication skills as appropriate. 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.

Under moderate supervision, the Regulatory and Start Up Specialist executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements  at the regional, or country level.Prepares and manages site documentation; reviews and negotiates site  documents and contracts with sites and sponsors; maintains, reviews, and reports on site performance metrics; serves as the primary point of contact for investigative sites; tracks completion of appropriate documents for sites; ensures contracts are fully executed; and establishes project timelines. Essential Functions• With moderate oversight and supervision, serve a Single Point of Contact (SPOC) to perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the  Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.• Prepare site documents, reviewing for completeness and accuracy.• Inform team members of completion of regulatory contractual. and other documents for individual sites.• Distribute completed documents to sites and internal project team members.• Update and maintain internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.• Review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents. Requires advanced knowledge within a specific discipline typically gained through extensive work experience and/or education. Qualifications• Bachelor's Degree Life sciences or a related field• 1 - 2 years of experience in a regulatory role in a CRO or pharma (not sites) and the following particular experience: CEP/CONEP - initial submission for Main Site and remaining sites, amendments to Main Site and Remaining sites, Notifications; ICF - Review and adaptation of local requirements (Country customization); ANVISA (MoH) - Initial DEEC Submission, Substantial Protocol Amendments, FAEC Update (Anvisa Clinical trial Form), annual study report (DEEC), Annual Safety Report (DDCM) • Advanced level of English skills • Great communication skills and ability to work in a team. This is a hybrid role. Offices are located in Sao Paulo, SP. 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 Client Service Coordinator 4 role acts as the Project Director and is responsible for Speaker Program team management, budget maintenance and reconciliation, executing project timelines, providing ongoing updates to internal team members and client contact(s), managing client system enhancement requests and resource management. Additionally, these responsibilities entail the facilitation/development of a multidisciplinary project team, interfacing with support services within the company, meeting customer and management expectations, and establishing strong client and faculty relationships. Responsibilities include, but are not limited to: Primary Responsibilities: Oversee initial planning and provision of all supporting project needs inclusive of but not limited to:Create, manage, and reconcile projects.System set-up and monitoringCreation and management of Project Assets such as speaker, rep and attendee communications, RSVP sites, eSign, etc.Manages and maintains content within internal and external portals.Prepare and monitor internal/external reports for clients and management to include but not limited to: Budget Expenditures, Reconciliations, Compliancy Reporting and Speaker Usage.Weekly/Monthly Monitoring ReportsProject Timeline/Schedule ExecutionDevelop and refine Standard Operating ProceduresApplication ChecklistsFaculty maintenance inclusive of nominations, contracts, and cap monitoringUploads and manages project budgets.Provides required budget reports.Completes requested budget transfers.Maintain, organize, and oversee each specifically assigned client’s compliance and budgetary guidelines.Support client audits as needed.Build & maintain strong, strategic relationships with various internal departments and clients.Participate in weekly calls with Application Development team to review and discuss system enhancements.Participate in client status calls.Participate in Quarterly Business Review meetings with client.Work with Creative for asset development & updates.Faculty maintenance inclusive of nominations, contracts, and cap monitoring.Support the talent management process to ensure the hiring, development, motivation & retention of high potential/high performers.Day to day oversight of direct reportsProvide effective leadership, mentorship, and development assistance for direct reports.Assist in the recruitment of employees by taking an active part in the interview process.Interview, hire and train new Program ManagersLead in the design and implementation of effective methods to train new team members, educate existing team members, and help to enhance performance and improve employee engagement and retention.Conduct 30-60-90-day reviews of new Program Managers to ensure job expectations are being met.Set clear, measurable performance expectations.Provide regular timely feedback to PCs.Conduct annual performance reviews to maximize performance against goals.In conjunction with HR, manage necessary performance improvement plans.Resolve employee conflicts, partnering with Human Resources, when necessary.Conduct monthly team calls to discuss success and challenges with the account/client.Conduct regular individual 1:1 calls with each direct report.Support in the training of new Project Directors on current client or other clients.Ensure technology is utilized appropriately to increase overall team efficiency & productivity.Adhere to all policies and procedures set forth by MedForce and clients and communicate them to each team members.Establish and maintain a basic knowledge of relevant healthcare products, disease states, and medical education.Perform other job-related duties and tasks as requested.Qualifications & Software/Technology: Minimum of 5 years industry related management experience inclusive of team management and industry specific softwareWell-developed skills in prioritizing, organizing, decision making, time management, and verbal/written communicationAdvanced skill in Microsoft Office Suite required – Excel, Word, PowerPoint & TeamsSuperior customer service (while working remote & also offsite)Dedicated and autonomous work ethic and accessibility for after-hours and/or offsite project supportKnowledge of PhRMA code guidelines, the Sunshine Act, state, and federal regulated compliancy guidelinesExperience in industry specific software such as Veeva Vault, Veeva Events Management, Adobe E-Sign, and Virtual Meeting PlatformsAbility to compare, contrast and quality check work, strong attention to detailCan present numerical data orally and in writing or through graphicsAbility to make clear, concise decisions and solve complex problemsCapable of establishing and maintaining a strong, strategic relationship with clients and internal stakeholdersHighly organized, adept at multi-tasking and prioritizing activitiesAbility to organize, plan and prioritize work in a fast-paced work environmentAbility to achieve goals and objectives in a timely fashionExperience leading a multidisciplinary team, strong management skills, and able to motivate others while maintaining a strong professional demeanorEducation Requirements A bachelor’s degree or equivalent education and/or work experienceTravel Requirements Possibility of internal and client travel (approximately 15%) based on business needs. This may include weekend and evening hoursIQVIA 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 $66,500.00 - $166,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job OverviewProvides high quality, on-time input to client projects in the life sciences field. Assignments typically require analysis and problem solving within an established framework. Essential Functions• Under direct supervision, assists with the review and analysis of client requirements or problems and assists in the development of client solutions.• Assists in the development of detailed documentation and specifications.• Under close supervision, performs quantitative or qualitative analyzes to assist in the identification of client issues and the development of client specific solutions.• Assists in the design and structure of presentations that are appropriate to the characteristics or needs of the audience.• Proactively develops a basic knowledge of consulting methodologies and the life sciences market through the delivery of consulting engagements and participation in formal and informal learning opportunities.• Engagement based responsibilities are assigned and closely managed by Consultants, Senior Consultants, Engagement Managers or Principals. Qualifications• Bachelor's Degree  Req• 1-3 years of related experience Req• Works willingly and effectively with others in and across the organization to accomplish team goals.• Knowledge and understanding of the fundamental processes of business, their interaction, and the impact of external/internal influences on decision making, growth and decline.• Knowledge of consulting methods, tools and techniques, related to one’s functional area.• Knowledge of current events and developments within an industry and major competitors.• Knowledge and understanding of the marketplace. Knowledge of professional/trade associations, key people and companies.• Effective time management 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. 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.