IQVIA

Role Purpose:•Responsible with the data monitoring, processing and validation of Internal Job DescriptionRole Purpose:• Responsible with the data monitoring, processing and validation of supplier’s datafocusing on stores and prescription information on a daily and weekly basis.• Supports US local office in prescription analysis and quality testing projects beforeloading it into production. Job Description:• Manages delivery of timelines and quality of output and creates documentation• Daily/Weekly/Monthly Reporting of analysis• Provides feedback to the teams involved whenever there’s a production issue.• Responsible for complying with internal quality standard• Responsible for complying with all information security policies and processes• Performs checks as outlined in the process document• Performs store monitoring and management, batch process management, imputationprocess, evaluation maintenance and overriding stores and suppliers• Follows quality processes thoroughly – checklists, standards etc.• Conducts quality checks across various data warehouses and tools for both Prescriberand Patient offerings. These tools may include, but not limited to, IDW, TDW, NDW,UDA, LRx, Mainframe, etc.• Performs functions as directed by the team leader Job Requirements:• Bachelor’s degree in Computer Science, Information Technology, Mathematics, IndustrialEngineering• Preferably with Statistical or Mathematics background and knowledge on Data Analytics• Strong interpersonal, written, and communication skills• Strong customer focus, an attention to detail and excellent analytical and problem solvingskills• Ability to work well with others cross functionally• Proven ability to achieve goals on time• Good analytical and problem-solving skills• Proficient in the use of Microsoft office application Intermediate to advance Excel Skills• Proficient in (at least) basic SQL skills• Proficient in SAS is an advantage but not required• Ability to work under time constraints and under minimum supervision.• Willing to work in the night shift. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

고용 형태: 1년 계약직 주요 업무1) 약국/의원 패널 관리 및 유통 관련 데이터 수집[약국 패널]• 월 1~2회 방문하여 거래명세표 수거 또는 e-Data 수취• 데이터 QC(품질 검증) 후 시스템 등록• 수거된 거래명세표 파일 정리 및 약국 반송[의원 패널]• 분기 1회 우편 또는 e-mail을 통한 데이터 수취• 데이터 QC(품질 검증) 후 시스템 등록• Query 발생 시 패널에 연락하여 이슈 확인 및 해결 2) 종합병원/의원 대상 제약사 커뮤니케이션 조사 패널 관리• 의사 대상 커뮤니케이션 및 패널 관리• 매월 진행되는 조사 안내 및 참여 독려• 조사 참여율, 응답 현황 관리• 패널 관련 기타 행정, 운영 업무 지원 자격 요건• 신입 또는 1년 이상의 경력 보유• 꼼꼼하고 책임감 있게 업무를 수행할 수 있는 분• 능동적이며 반복적인 업무에도 성실히 임하는 성향• 원활한 커뮤니케이션 능력 보유• 정해진 프로세스 및 절차에 따라 업무를 수행하고, 기본적인 이슈를 스스로 해결할 수 있는 분• 의료 제품 또는 병·의원 환경 관련 업무 경험 우대 [추천 컨텐츠]1.What does it mean to be IQVIAN?(video)2.아이큐비아ㅣ나만 몰랐던 (진짜) 포브스 선정 '세계 최고의 직장'(video) [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.

IQVIA Laboratories is a global leader in drug discovery and development laboratory services, offering a comprehensive suite of central laboratory and specialty biomarker services.In a complex environment, we work closely with customers to understand their unique needs and provide the right mix of in-depth scientific and operational expertise, specialty lab services and next-generation lab technologies to achieve their goals with efficiency. At each stage of drug discovery and development, the IQVIA Laboratories team is ready to deliver timely and reliable outcomes, turning innovative ideas into groundbreaking milestones for patients in need.  Job OverviewSecure and retain business through professional, consultative, proactive sales activities directed at decision-makers and decision influencers at existing and new clinical sponsors. Essential Functions• Actively prospect and leverage potential new business opportunities within specified customer account(s).• Cultivate strong, long-term relationships with key decision-makers within Account and develop in-depth knowledge of the customer organization.• Maintain general knowledge of all IQVIA services for appropriate cross-sell opportunities.• Aggressively pursue awareness of competitive activities, positioning and pricing, which includes specific reasons for awards and non-awards.• Identify and respond to customer needs in order to define potential opportunities. Propose appropriate strategy/solution to customer.• Coordinate with contracts/proposals to develop proposal.• Work with operations and functional managers to identify sales team and prepares and leads the sales presentation. Educate team participants in customer culture, operational needs/methods and sales techniques needed to close the sale.• Handle follow-up related to the sale and drive completion of contractual documents.• Adapt successful strategies and tactics to meet market demands and financial targets.• Maintain high visibility within customer organization. Monitor customer satisfaction by communicating regularly with customer.• Establish and execute a comprehensive sales plan for each target account. Ensure appropriate strategy/solution is proposed to customer. Monitor actions and results against plans.• Analyze potential opportunities and develop sales plans for each target account. Ensure appropriate strategy/solution is proposed to customer.• Monitor actions and results against plans.• Record all customer sales related activities in CRM system.• Prepare sales activity report for Sales Management as required.• Serve as a liaison between the customer and technical and operational groups at IQVIA, Inc. Qualifications• Master or Bachelor's Degree in Medical, Pharmaceutical, Biology, Business Management • 10+ years related experience, including 3+ years of relevant industry (CRO/Pharmaceutical) and/or sales experience • Fluent in both Korean and English• Proven track record at mid-level and high-level contacts• Strong organizational, planning, project management skills• A developing record of customer contacts at the outsourcing, procurement and mid - management level• Excellent Business/Industry awareness and a thorough understanding of industry trends and impact on the business• Excellent analytical skills in assessing and interpreting customer business data• Ability to maintain demanding timelines• Ability to influence others internally and externally• Adaptability and flexibility to changing priorities• Demonstrated ability to work creatively in a fast-paced environment• Exceptional attention to detail and ability to work simultaneously on multiple priorities• Ability to work independently and as a team player• Excellent skills using Microsoft Office Suite: MS PowerPoint, MS Word, and MS Excel• Excellent oral and written communication skills• Ability to establish and maintain effective working relationships with coworkers, managers and clients [추천 컨텐츠]1.What does it mean to be IQVIAN?(video)2.아이큐비아ㅣ나만 몰랐던 (진짜) 포브스 선정 '세계 최고의 직장'(video) [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.

IQVIA Biotech is seeking a Clinical Project Manager with at least 2 years experience in project management in Cardiovascular, Renal and/or Metabolic. IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster. Job Overview Clinical Project Managers are key to delivering clinical trials that bring new therapies to patients faster. As an essential member of the core project team, you will oversee the planning, execution, and delivery of clinical studies to meet contractual, quality, and financial objectives. This role combines operational excellence with strategic leadership, leveraging therapeutic expertise and IQVIA’s innovative solutions to ensure success. Essential Functions Lead and manage smaller, less complex regional studies or assigned portions of global studies.Participate in bid defense presentations and collaborate with Business Development.Develop integrated study management plans and ensure compliance with SOPs, policies, and regulatory requirements.Drive execution of clinical studies per contract, optimizing speed, quality, and cost.Set objectives for project teams, monitor performance, and provide feedback.Collaborate with cross-functional teams to achieve milestones and resolve study issues.Monitor progress against contract and proactively present updates to stakeholders.Identify and manage risks, implement corrective and preventive actions, and ensure quality standards.Serve as primary or backup contact for customers and vendors, fostering strong relationships.Ensure financial success through forecasting, scope management, and revenue acceleration.Mentor junior team members and support staff development.Qualifications Education: Bachelor’s degree in Life Sciences or related field required.Experience: Minimum 5 years in clinical research, including 1+ years in project management.Knowledge: Strong understanding of ICH-GCP, clinical trial conduct, and regulatory requirements; therapeutic expertise preferred.Technical Skills: Proficiency in MS Office; familiarity with CTMS and EDC systems.Soft Skills:Excellent communication and presentation skills.Strong leadership and decision-making ability.Effective planning, prioritization, and problem-solving skills.Ability to manage cross-functional teams and work across geographies.Other: Ability to travel as required; strong financial acumen for project budgeting and forecasting.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Are you looking for an opportunity in Clinical Research?  Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly?  If so, come and join us - IQVIA are looking Clinical Research Coordinator. This role has an immediate start working 24 hours a week for a period of 6 months to support the site. The study coordinator should have experience clinically or nursing background as tasks includes perform EKG, collect vital signs. This is an excellent opportunity if you have experience working as a SC As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data. Day to day responsibilities will include: Verifying and/or correcting research study information on source documents; researching queries and variances; providing feedback to the site data collector Accurate input of trial data into the Electronic Data Capture (EDC) system and tracking visits and procedures completed against budget in the clinical trial management system (CTMS) Preparing and maintaining study files, and timely submission of information Collecting, submitting and assisting in maintaining relevant regulatory and ethics documents Scheduling visits with research subjects, generating appropriate reports and documentation Other administrative support functions such as reception, office organization and supply management.    We are looking for candidates with the following skills and experience: Bachelor's degree in life sciences Basic knowledge of clinical trials, study coordinator experience Availability to work based in São Paulo/SP Availability to work part-time (24 hours per week) Availability to work in a fixed term contract (6 months) IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.• Collaborate and liaise with study team members for project execution support as appropriate.• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications• High School Diploma or equivalent Degree in scientific discipline or health care preferred.• Requires at least 2 years of year of on-site monitoring experience.• Equivalent combination of education, training and experience may be accepted in lieu of degree.• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.• Good therapeutic and protocol knowledge as provided in company training.• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).• Written and verbal communication skills including good command of Arabic and English language.• Organizational and problem-solving skills.• Effective time and financial management skills.• Ability to establish and maintain effective working relationships with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

A la croisée de deux univers, la santé et les nouvelles technologies, IQVIA est l’expert des données de santé depuis plus de 60 ans et dans 140 pays. IQVIA s’appuie sur ses bases de données uniques, sur son expertise et sur ses outils d’analyse pour apporter des services et des solutions de conseil aux acteurs du système de santé. Grace à l’utilisation de méthodes innovantes telles que l’intelligence artificielle, IQVIA contribue à l’amélioration de la prise en charge des patients et au développement de la médecine de demain. Nous participons à la mise en place d'un système de santé plus moderne, plus efficace et plus adapté aux besoins de chacun. Le Site Management recherche pour intégrer ses équipes, un : Stagiaire attaché de recherche clinique (H/F) Date de démarrage : ASAP Basé dans nos locaux de La Défense, à Courbevoie (92) Au sein des équipes projets, dans les locaux IQVIA, l’ARC est supervisé par des chefs de projet expérimentés. Vous aurez pour mission principale d’assurer la mise en œuvre et le suivi d’études observationnelles avec primary data collection, selon les procédures opératoires standardisées. Assurer le monitoring de la partie Française sous la coordination du chef de projet (formation des centres, monitoring des données et clôture)Support à la coordination des ARC prestatairesSupport à la coordination de l’étude : rédaction newsletter, Reporting clientCoordination d’activités Quality et de process d’optimisationMonitoring des centres : récupération des queries, relance inclusion et support dans la réalisation de l’étude.Gestion de Projet, réalisation de propositions…En formation spécialisée ARC, vous recherchez une entreprise reconnue pour son expertise en rechercher clinique et qui sera en mesure de vous accompagner dans le développement du panel de compétences associées. 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.

Our MedTech Device Field Collection Associate experiences a unique opportunity for collecting reprocessed medical equipment in a hospital. You will be working with surgical, non-invasive and vascular equipment within areas of the hospital such as Operating Rooms and Sterile Processing Departments. This is a great opportunity for you to gain medical experience!  You will have a flexible schedule and an opportunity to grow and expand into new opportunities while earning supplemental income and learning about the medical device industry.   What you will be doing in the role: Visit assigned hospitals weekly to collect products to be reprocessed Package and ship product to client manufacturing plant Document and log daily collections totals Notify the local Sales team of shipping supply needs Appropriate PPE is provided to all employees prior to the start of assignments. Available to work approximately 12-15 hours a week Training for this role will be provided and is paid Job Requirements:   An active and unrestricted driver license is required for this position  Minimum High school diploma or equivalent Reliable vehicle for transportation Must be comfortable with basic software programs and Microsoft operating system  Excellent customer service skills and strong attention to detail Ability to lift 30-50 lbs Ability to clear hospital vendor credentialing requirements, including proof of vaccination status, required  Travel Requirement: Travel locally for up to 2-3 hours to support customer needs Must have an active driver license and a personal vehicle to use for job related assignments Travel time is paid, as is mileage Preferred Attributes: Experience in healthcare, general labor, warehouse or customer service, is beneficial for this position. Ability to work independently in customer settings with minimal supervision. IQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities. Benefits: This position is not eligible for our Medical Benefits. Vaccine/Immunization/Hospital Credentialing Requirement: A required function of this job requires individuals to enter various healthcare facilities.  Thus, upon selection, individuals must complete healthcare facility credentialing process.  To obtain credentials, individuals must meet the immunization requirements specified by the facility.  Individuals are typically required to have completed/up to date: Measles, Mumps & Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria & Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series (heavily enforced by most facilities, some require booster(s)). Please note, IQVIA complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons, however, our client’s requirements may supersede this.  *Please note: No relocation is being offered for this role. Candidate must live locally to be considered. Due to the nature of this role, it is not eligible for Visa sponsorship. LFT1 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 $51,400.00 - $128,400.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Research Nurse Location: Middlesborough24 hours per week | 6 months contract (potential to be extended) | Start: July 2026 IQVIA is hiring an experienced Clinical Research Nurse to support a hypertension and cardiovascular clinical trial in Middlesborough. What you’ll be doing:Perform a variety of complex clinical procedures on subjects including but not limited to vital signs, phlebotomy, administration of IP, ECG etcCollect, record, and report clinical data Assist in study enrollment by recruiting, screeningPerform clinical set-up and preparation for the study Perform data entry, data quality checking, and query resolutionWhat we’re looking for:Registered Nurse (active registration with NMC)Proven experience with phlebotomyMinimum 3 years’ Clinical Research Nurse experienceStrong clinical trial knowledge and hands-on skills (IP, ECGs, labs)Excellent organisation, communication, and attention to detailWhy IQVIA?Work with a global leader in clinical research on impactful studies in a supportive, professional environment. Apply now if you meet the essential experience criteria and are ready to make a difference in this space. #LI-HCPN #LI-CES #LI-DNP #LI-NS1 #LI-Onsite IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and life sciences consulting. We help healthcare stakeholders drive innovation and improve patient outcomes worldwide. By combining data, science, and human ingenuity, we deliver impactful solutions that shape the future of healthcare. Why Join Our Professional Trainee, Market Access Program? Our Professional Trainee Program offers a unique opportunity to gain hands-on experience in healthcare consulting, with a focus on Market Access strategy. You’ll receive structured training, mentorship from experienced consultants, and exposure to real client projects. As part of our collaborative and flat team structure, you will work closely with senior leaders while developing core consulting and analytical skills. High-performing trainees will be considered for a full-time Associate role upon successful completion of the program. What You’ll Experience Hands-on consulting experience solving real healthcare business challenges Structured training in market access strategy, data analysis, and storytelling Direct exposure to senior leaders, client work, and high-impact projects Advanced skill-building in Excel modeling, PowerPoint, and data-driven insights Mentorship, feedback, and a clear path to a full-time Associate role Key Responsibilities Conduct high-quality quantitative and qualitative analyses to address client business questions Leverage large datasets (“big data”) to identify trends, generate insights, and support actionable recommendations Perform primary and secondary research across markets, payers, physicians, patients, and competitors Support the development of predictive models related to pricing, contracting strategies, patient affordability, and product utilization Translate complex analyses into clear, concise insights and client-ready deliverables (presentations, reports, etc.) Actively contribute to internal discussions, problem-solving, and project execution Maintain high quality standards by applying quality control (QC) processes across all work Manage time effectively, meet deadlines, and communicate progress and challenges proactively Build foundational knowledge of the healthcare industry and consulting practices Qualifications Recently graduated or about to receive diploma in Bachelor’s or Master’s degree in a relevant field with strong affinity for data and analytics. Fluency in English (B2–C1 minimum; strong business communication preferred) Advanced proficiency in Excel. SQL, Python or other similar tools are a plus. Genuine interest in healthcare, pharmaceuticals, and consulting Willingness to travel occasionally (

We are seeking Laboratory Project Services Coordinator to join IQVIA Laboratories at Marietta, GA.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary:Support the Project Manager and project team by performing routine procedures and coordinating study activities across the full study lifecycle, from start-up through close-out. Help ensure project deliverables, laboratory monitoring, and customer expectations are met in line with standard operating procedures, policies, and protocol requirements. What You'll Be Doing:Support study setup and planning activities, including attending meetings, preparing minutes and action logs, and creating protocol-specific laboratory instruction documentsAssist with protocol-specific Laboratory Centralized Monitoring setup under the supervision of the Project ManagerPerform routine study tasks such as site loading, Investigator Portal access, kit shipments, and day-to-day study performance monitoringWork with internal and external teams to resolve queries, protocol questions, issues, and escalations in a timely mannerUse status reports, monitoring tools, and study outputs to identify trends and provide feedback on site and service performanceCoordinate and communicate with stakeholders, including leading customer communications when the Project Manager is absentSupport project close-out activities and contribute to meetings, audits, inspections, and study training as needed What We Are Looking For:High School Diploma or equivalent required; Bachelor’s Degree in life sciences or related field preferred1+ years relevant experience (Clinical, Medical or Healthcare industry preferred)Computer proficiency in word processing, presentation and spreadsheet applicationsAbility to support Investigator Portal access, site loading, kit shipments, and Laboratory Centralized Monitoring requirementsOther 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, communication, organizational, and time management skillsDemonstrated ability to handle multiple competing priorities, think critically, and solve problems effectivelyAbility to work in a fast-paced environment and establish and maintain effective working relationships with coworkers and managersStrong written and verbal communication skills including good command of English languageMust be able to comply with all applicable standards as required by the companyAbility to lift up to 50 lbs, frequent standing and walking, occasional sitting, close eye work requirement (computer, typing, reading small prints). Physical demands vary depending on assigned work area and work tasks. Occasional exposure to cold temperatures. What We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.To learn more about our benefits, visit https://jobs.iqvia.com/benefits.If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $43,000.00 - $89,500.00. 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.

We are seeking Associate Laboratory Project Services Manager to join IQVIA Laboratories at Marietta, GA.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary:Under general direction, manage all laboratory aspects of assigned clinical trial projects for a customer or specific program and serve as the main point of contact throughout the study lifecycle. Lead study setup, monitoring, communication, and closeout activities to ensure delivery aligns with standard operating procedures, policies, and good practices. What You'll Be Doing:Lead study setup activities including protocol and budget review, project planning, milestone tracking, and risk, issue, and action managementPartner with Study Setup teams to support quality database setup and oversee the preparation of protocol-specific documentation and presentation materialsMonitor project management plans, timelines, deliverables, and study documentation across startup, maintenance, and closeoutManage study scope changes, support budget oversight, and address quality or service-related issues through timely resolution and process improvementBuild and maintain strong customer relationships while serving as the primary escalation point for study-level issuesCoordinate meetings, reporting, customer survey follow-up, and ongoing health checks to support project success and customer satisfactionDeliver study training to sites, CRAs, and customers and represent the company at investigator meetings, audits, inspections, and other internal or external meetings What We Are Looking For:Bachelor's Degree in Life Sciences and/or related field preferred2-3 years of experience in clinical trials/ hospital-funded research, project management or laboratory environment preferred.Working knowledge of Project Management processes and central laboratory operations including kits/supplies, logistics, laboratory operations, 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 customer management skills with the ability to establish and maintain effective working relationships with coworkers, managers, customers, and sitesStrong written and verbal communication skills, including good command of English languageDemonstrated ability to work in a fast-paced environment while maintaining strong organizational skills and meeting deadlinesWorking understanding of medical and clinical research terminologyAbility to coordinate cross-functional operational activities and triage study-specific issues effectively 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 Laboratory Project Services Manager to join IQVIA Laboratories at Marietta, GA.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary:Provide project-related support and assistance for assigned projects and project teams across the full study lifecycle, including start-up, maintenance, and closeout. Ensure all work is conducted in line with standard operating procedures, policies, and good practices while helping teams maintain efficient and compliant project delivery. What You'll Be Doing:Support assigned projects and project teams throughout the study lifecycleAssist with project start-up, maintenance, and closeout activitiesCoordinate project-related procedures and administrative tasksEnsure project documentation and activities align with standard operating procedures and policiesMaintain compliance with good practices and internal quality standardsCollaborate with cross-functional teams to support study execution and project continuityMonitor assigned project tasks and follow up on required actions to support timelines What We Are Looking For:Minimum education requirement was not specified in the internal job information providedYears of experience in relevant fields were not specified in the internal job information providedExperience supporting project procedures and study lifecycle activities in a laboratory or research environmentKnowledge of standard operating procedures, policies, and good practices related to project support and study executionOther Equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Strong organizational skills with the ability to manage multiple project activities simultaneouslyEffective communication and collaboration skills across project teams and stakeholdersHigh attention to detail and commitment to quality, compliance, and process consistencyAbility to work independently while supporting broader team objectivesProblem-solving mindset with the ability to follow procedures and escalate issues appropriately 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 Associate Laboratory Project Services Manager to join IQVIA Laboratories at Marietta, GA.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary:Manage laboratory aspects of assigned clinical trial projects and serve as the main point of contact for customers across study startup, maintenance, and closeout. Drive project planning, timelines, risk management, and cross-functional coordination to deliver studies in line with standard operating procedures, policies, and good practices. What You'll Be Doing:Lead study setup activities, including protocol and budget review, project planning, milestone tracking, and risk, issue, and action managementPartner with study setup teams to support high-quality database configuration and oversee protocol-specific documentation and presentation materialsMonitor the Project Management Plan, timelines, deliverables, and study documentation throughout the full project lifecycle, including eTMF filingManage study scope changes, budget tracking, service-related issues, and lessons learned to support quality delivery and continuous improvementBuild and maintain strong customer relationships while coordinating communication across operational teams and serving as an escalation point for study-level issuesRepresent the company at investigator meetings, audits, inspections, and other internal or external meetings as requiredProvide study training to sites, CRAs, and customers, and support the development of less experienced staff What We Are Looking For:Bachelor's Degree in Life Sciences and/or related field preferred2+ years of clinical or research industry experience, including 1 year project management / project set up experienceDemonstrated computer proficiency with Microsoft Office and company systems, or equivalent experience with similar Centralized Laboratory systems preferredWorking knowledge of Project Management processes and central laboratory operations, including kits/supplies, logistics, laboratory operations, specimen storage, data reporting and transfers, and site alerts preferredWorking understanding of medical and clinical research terminologyOther Equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Strong interpersonal and customer management skills with the ability to build trusted working relationshipsStrong written and verbal communication skills including good command of English languageDemonstrated ability to work in a fast-paced environment while staying organized and meeting deadlinesAbility to establish and maintain effective working relationships with coworkers, managers and customers What We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.To learn more about our benefits, visit https://jobs.iqvia.com/benefits.If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $64,200.00 - $133,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Estamos buscando un Operador de Base de Datos Nativo Español para llevar a cabo el mantenimiento de nuestra base de datos de atención médica en español. Si estás buscando una oportunidad increíble en una empresa multinacional, únete a nuestro equipo multicultural con más de 54 nacionalidades diferentes. Si deseas desempeñar un papel clave en un equipo multicultural, dinámico y comprometido, esta es una gran oportunidad. Funciones esenciales: • Actualizar las bases de datos de referencia con nuevos productos y cambios en los mercados de los países de habla hispana, asegurando la calidad de los datos: clasificar productos, estandarizar y agrupar datos siguiendo las jerarquías y reglas comerciales de la empresa. • Identificar los cambios necesarios en el archivo de referencia existente. • Trabajar junto con las oficinas locales para identificar cuándo y cómo corregir datos inexactos, eliminar datos o agregar nuevas entradas para hacer los archivos de referencia más completos. • Identificar y resolver excepciones y problemas rutinarios. • Realizar el control de calidad de los datos mantenidos y aplicar las correcciones necesarias. • Mantener la documentación de los procesos y procedimientos. Funciones esenciales: • Actualizar las bases de datos de referencia con nuevos productos y cambios en los mercados de los países de habla hispana, asegurando la calidad de los datos: clasificar productos, estandarizar y agrupar datos siguiendo las jerarquías y reglas comerciales de la empresa. • Identificar los cambios necesarios en el archivo de referencia existente. • Trabajar junto con las oficinas locales para identificar cuándo y cómo corregir datos inexactos, eliminar datos o agregar nuevas entradas para hacer los archivos de referencia más completos. • Identificar y resolver excepciones y problemas rutinarios. • Realizar el control de calidad de los datos mantenidos y aplicar las correcciones necesarias. • Mantener la documentación de los procesos y procedimientos. Habilidades y otros requisitos: • Nativo en español y alto nivel de inglés. • Experiencia en mantenimiento y actualización de bases de datos es un plus. • Buen manejo de Excel. • Formación Profesional y conocimientos administrativos •Trabajo desde Oficina (Madrid  -  Condesa de Venadito) 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.

Estamos buscando un Operador de Base de Datos Nativo Español para llevar a cabo el mantenimiento de nuestra base de datos de atención médica en español. Si estás buscando una oportunidad increíble en una empresa multinacional, únete a nuestro equipo multicultural con más de 54 nacionalidades diferentes. Si deseas desempeñar un papel clave en un equipo multicultural, dinámico y comprometido, esta es una gran oportunidad. Funciones esenciales: • Actualizar las bases de datos de referencia con nuevos productos y cambios en los mercados de los países de habla hispana, asegurando la calidad de los datos: clasificar productos, estandarizar y agrupar datos siguiendo las jerarquías y reglas comerciales de la empresa. • Identificar los cambios necesarios en el archivo de referencia existente. • Trabajar junto con las oficinas locales para identificar cuándo y cómo corregir datos inexactos, eliminar datos o agregar nuevas entradas para hacer los archivos de referencia más completos. • Identificar y resolver excepciones y problemas rutinarios. • Realizar el control de calidad de los datos mantenidos y aplicar las correcciones necesarias. • Mantener la documentación de los procesos y procedimientos. Funciones esenciales: • Actualizar las bases de datos de referencia con nuevos productos y cambios en los mercados de los países de habla hispana, asegurando la calidad de los datos: clasificar productos, estandarizar y agrupar datos siguiendo las jerarquías y reglas comerciales de la empresa. • Identificar los cambios necesarios en el archivo de referencia existente. • Trabajar junto con las oficinas locales para identificar cuándo y cómo corregir datos inexactos, eliminar datos o agregar nuevas entradas para hacer los archivos de referencia más completos. • Identificar y resolver excepciones y problemas rutinarios. • Realizar el control de calidad de los datos mantenidos y aplicar las correcciones necesarias. • Mantener la documentación de los procesos y procedimientos. Habilidades y otros requisitos: • Nativo en español y alto nivel de inglés. • Experiencia en mantenimiento y actualización de bases de datos es un plus. • Buen manejo de Excel. • Formación Profesional y conocimientos administrativos •Trabajo desde Oficina (Madrid  -  Condesa de Venadito) 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.

Estamos buscando un Operador de Base de Datos Nativo Español para llevar a cabo el mantenimiento de nuestra base de datos de atención médica en español. Si estás buscando una oportunidad increíble en una empresa multinacional, únete a nuestro equipo multicultural con más de 54 nacionalidades diferentes. Si deseas desempeñar un papel clave en un equipo multicultural, dinámico y comprometido, esta es una gran oportunidad. Funciones esenciales: • Actualizar las bases de datos de referencia con nuevos productos y cambios en los mercados de los países de habla hispana, asegurando la calidad de los datos: clasificar productos, estandarizar y agrupar datos siguiendo las jerarquías y reglas comerciales de la empresa. • Identificar los cambios necesarios en el archivo de referencia existente. • Trabajar junto con las oficinas locales para identificar cuándo y cómo corregir datos inexactos, eliminar datos o agregar nuevas entradas para hacer los archivos de referencia más completos. • Identificar y resolver excepciones y problemas rutinarios. • Realizar el control de calidad de los datos mantenidos y aplicar las correcciones necesarias. • Mantener la documentación de los procesos y procedimientos. Funciones esenciales: • Actualizar las bases de datos de referencia con nuevos productos y cambios en los mercados de los países de habla hispana, asegurando la calidad de los datos: clasificar productos, estandarizar y agrupar datos siguiendo las jerarquías y reglas comerciales de la empresa. • Identificar los cambios necesarios en el archivo de referencia existente. • Trabajar junto con las oficinas locales para identificar cuándo y cómo corregir datos inexactos, eliminar datos o agregar nuevas entradas para hacer los archivos de referencia más completos. • Identificar y resolver excepciones y problemas rutinarios. • Realizar el control de calidad de los datos mantenidos y aplicar las correcciones necesarias. • Mantener la documentación de los procesos y procedimientos. Habilidades y otros requisitos: • Nativo en español y alto nivel de inglés. • Experiencia en mantenimiento y actualización de bases de datos es un plus. • Buen manejo de Excel. • Formación Profesional y conocimientos administrativos •Trabajo desde Oficina (Madrid  -  Con 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.

Estamos buscando un Operador de Base de Datos Nativo Español para llevar a cabo el mantenimiento de nuestra base de datos de atención médica en español. Si estás buscando una oportunidad increíble en una empresa multinacional, únete a nuestro equipo multicultural con más de 54 nacionalidades diferentes. Si deseas desempeñar un papel clave en un equipo multicultural, dinámico y comprometido, esta es una gran oportunidad. Funciones esenciales: • Actualizar las bases de datos de referencia con nuevos productos y cambios en los mercados de los países de habla hispana, asegurando la calidad de los datos: clasificar productos, estandarizar y agrupar datos siguiendo las jerarquías y reglas comerciales de la empresa. • Identificar los cambios necesarios en el archivo de referencia existente. • Trabajar junto con las oficinas locales para identificar cuándo y cómo corregir datos inexactos, eliminar datos o agregar nuevas entradas para hacer los archivos de referencia más completos. • Identificar y resolver excepciones y problemas rutinarios. • Realizar el control de calidad de los datos mantenidos y aplicar las correcciones necesarias. • Mantener la documentación de los procesos y procedimientos. Funciones esenciales: • Actualizar las bases de datos de referencia con nuevos productos y cambios en los mercados de los países de habla hispana, asegurando la calidad de los datos: clasificar productos, estandarizar y agrupar datos siguiendo las jerarquías y reglas comerciales de la empresa. • Identificar los cambios necesarios en el archivo de referencia existente. • Trabajar junto con las oficinas locales para identificar cuándo y cómo corregir datos inexactos, eliminar datos o agregar nuevas entradas para hacer los archivos de referencia más completos. • Identificar y resolver excepciones y problemas rutinarios. • Realizar el control de calidad de los datos mantenidos y aplicar las correcciones necesarias. • Mantener la documentación de los procesos y procedimientos. Habilidades y otros requisitos: • Nativo en español y alto nivel de inglés. • Experiencia en mantenimiento y actualización de bases de datos es un plus. • Buen manejo de Excel. • Formación Profesional y conocimientos administrativos •Trabajo desde Oficina (Madrid  -  Condesa de Venadito) 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.

Estamos buscando un Operador de Base de Datos Nativo Español para llevar a cabo el mantenimiento de nuestra base de datos de atención médica en español. Si estás buscando una oportunidad increíble en una empresa multinacional, únete a nuestro equipo multicultural con más de 54 nacionalidades diferentes. Si deseas desempeñar un papel clave en un equipo multicultural, dinámico y comprometido, esta es una gran oportunidad. Funciones esenciales: • Actualizar las bases de datos de referencia con nuevos productos y cambios en los mercados de los países de habla hispana, asegurando la calidad de los datos: clasificar productos, estandarizar y agrupar datos siguiendo las jerarquías y reglas comerciales de la empresa. • Identificar los cambios necesarios en el archivo de referencia existente. • Trabajar junto con las oficinas locales para identificar cuándo y cómo corregir datos inexactos, eliminar datos o agregar nuevas entradas para hacer los archivos de referencia más completos. • Identificar y resolver excepciones y problemas rutinarios. • Realizar el control de calidad de los datos mantenidos y aplicar las correcciones necesarias. • Mantener la documentación de los procesos y procedimientos. Funciones esenciales: • Actualizar las bases de datos de referencia con nuevos productos y cambios en los mercados de los países de habla hispana, asegurando la calidad de los datos: clasificar productos, estandarizar y agrupar datos siguiendo las jerarquías y reglas comerciales de la empresa. • Identificar los cambios necesarios en el archivo de referencia existente. • Trabajar junto con las oficinas locales para identificar cuándo y cómo corregir datos inexactos, eliminar datos o agregar nuevas entradas para hacer los archivos de referencia más completos. • Identificar y resolver excepciones y problemas rutinarios. • Realizar el control de calidad de los datos mantenidos y aplicar las correcciones necesarias. • Mantener la documentación de los procesos y procedimientos. Habilidades y otros requisitos: • Nativo en español y alto nivel de inglés. • Experiencia en mantenimiento y actualización de bases de datos es un plus. • Buen manejo de Excel. • Formación Profesional y conocimientos administrativos •Trabajo desde Oficina (Madrid  -  Condesa de Venadito) IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Job OverviewWith global impact and oversight, manage a department of Biostatistics and Statistical Programming staff ensuring that target productivity (project allocations, utilization, and output) levels are met.  May fulfill the role of site head or functional head within a site.  Manage direct personnel reports typically consisting of Manager to Associate Director level staff from each function. Participate in sales meetings as required and oversees departmental proposal preparation. Monitors budget and scope of within-office projects and takes action necessary to maximize realization. Ensure that departmental staff contribute to intra- and interdepartmental process improvement to achieve "best practices". Ensure that appropriate levels of professional development and training are provided to staff. Serve as a Biostatistical resource for the department, ensuring scientific integrity in the application of statistical methodology to clinical trials.  Provide statistical direction, technical oversight, or consultancy on major projects or on projects involving particularly complex statistical analyses. Represent clients at the Food and Drug Administration (FDA) or other scientific meetings as required. Essential Functions• Production of High-Quality Deliverables: Ensure the high quality and timeliness of deliverables from the Biostatistics department. Oversee and ensures the high quality level of the Biostatistics expert review process. Leadership:  Where relevant, may include:  Serve as a statistical consultant for other members of the department and staff members from other Biostatistics departments within the company. Maintain knowledge and awareness of developments in Biostatistics and clinical trial methodology, and regulatory requirements that impact analyses. Represent clients at meetings with regulatory agencies or other regulatory meetings, may participate as a member of a Data and Safety Monitoring Committee. May participate in independent research activities, teaching opportunities, presentations, and preparation of manuscripts for publication, as approved. May participate as high level lead biostatistician on major project(s) including developing/reviewing protocols, preparing analysis plans, and writing sections of joint clinical/statistical reports, integrated summaries and/or new drug application (NDA) sections, as required. Provide advanced technical expertise for internal and external clients. Assist and contribute to governance structures where relevant.• Management:  Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work, appraising performance and guiding professional development, rewarding and disciplining employees, addressing employee relations issues and resolving problems, ensure compliance with operational components (e.g. Standard Operating Procedures (SOPs), Timesheets). Approve actions on human resource matters. Accountable for the project level work of staff including awareness of resource reports/strategy. Responsible for guiding leads toward financial success at a study level.• Compliance:  Ensures compliance with strategy and initiatives. Implements strategy and initiatives and collects feedback from the implementation (e.g. metrics). Develop and/or provide training to staff across the business unit. May provide feedback to draft strategy and initiatives.• Financials:  Client leaders are accountable for controlling cost and maximizing revenue at a client/service group level. Regarding ownership of operational components, ensure remit is in line with or maximizes business unit needs to control costs and maximize revenue recognition. Participate in monthly project review and operations meetings.• Strategy and Initiatives:  Defines overall strategy and initiatives for service group or client in line with business segment owners and business unit expectations. Contributes to global strategy and Initiative discussions with the Senior Directors. May provide training. Owns/Project Manages defined strategies and initiatives from the Senior Directors including delegation of components of strategy and initiatives to Associate Directors, when it is of when appropriate. Collaborate with other business units to develop strategies for process improvement. Customer:  Develop, maintain and expand key client relationships. Act as Client/service group owner where significant business unit portfolio presence exists. Own operational pieces of the business segment (e.g. resource management for a business segment, recruitment management for a business segment). Take responsibility for client/service group level strategies and initiatives. Identify opportunities for additional business from existing clients and seek to develop new clients/service offerings.• Risk Management:  Manage risks to project delivery and/or quality. Able to manage and accountable for all study level escalations. When managing leads: operate as an escalation point for Biostatistical team leads• Proposals:  Participate in sales meetings, as required. Contribute to marketing materials. Create budgets, propose adjustments, and be able to discuss budget assumptions with clients, as well as the ability to understand and discuss pricing models. Write proposals and budgets at a study/submission level (may have experience drafting partnership proposals). Attend project defenses that could potentially expand the account and act as Primary Point of Contact (POC) for New Account Defenses. Explore new business growth opportunities and provide input into strategies that will enable Biostatistics to capitalize on those opportunities. Take a leadership role in project defenses that could potentially expand the account and Primary Point of Contact (POC) for New Account Defenses. Explore new business growth opportunities and provide input into strategies that will enable Bios to capitalize on those opportunities. Qualifications• Bachelor's Degree Biostatistics or related field and 11 years relevant experience including 4 years experience managing staff Req Or• Master's Degree Biostatistics or related field and 11 years relevant experience including 4 years experience managing staff Req Or• Ph.D. Biostatistics or related field and 7 years relevant experience including 4 years experience managing staff Req• Typically requires 11+ years of prior relevant experience, including 4 years experience managing staff or equivalent combination of education, training and experience.• Requires broad management knowledge to lead teams, and well as the ability to influences others outside of own job area regarding policies, procedures, and goals.• Familiarity with most complex statistical methods that apply to Phase I-IV clinical trials.• In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.• Excellent written and oral communication skills with excellent interpersonal skills.• Excellent problem solving skills.• Excellent presentation skills.• Excellent judgment/decision making.• Leadership and line management skills.• Some demonstrated success of operation within senior/executive management teams.• Ability to establish and maintain effective working relationships with coworkers, managers and clients.• Working knowledge of relevant Data Standards (such as Clinical Data Interchange Standards Consortium (CDISC)/ADaM). IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Job Overview IQVIA is hiring a clinical project manager to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment of a prominent pharma company. In this role, the clinical project manager will be responsible for end-to-end project delivery of real-world observational studies within the oncology therapeutic area. It is important for this individual to have experience working in observational research across primary and secondary data collection study designs as well as leading clinical studies independently. Who do you work with? Epidemiologists, data science, and clinical leads to deliver project specific goals and timelines Vendors to communicate status of deliverables and workflow Program and business leads to manage full portfolio of projects What are you great at? Independently executing observational and real-world studies while balancing speed, quality, and cost Leading cross-functional teams to achieve milestones and resolve study issues Proactively identifying risks and implementing mitigation plans Communicating clearly with stakeholders, including preparing and presenting project updates to leadership Good understanding of project financials including experience managing, contractual obligations and implications Driving operational excellence and strategic partnership with clients Managing vendors effectively across different sourcing models (in-house, hybrid, outsourced) Bringing clarity to complex or ambiguous situations and making informed decisions Results-oriented approach to work towards delivery and output Strong organizational, prioritization, and time management skills Ability to operate effectively in a matrixed, fast-paced, and evolving environment Your responsibilities may include:  Leading global, cross-functional observational study teams and owning delivery of contracted scope, timelines, and quality Developing study documentation, including project management plans Ensuring consistent use of study tools, training materials, and compliance with SOPs, policies, and procedures Monitoring study progress and financial performance; supporting forecasting and change control as needed Lead project vendor management related activities and communications per project requirements Anticipating operational and quality risks, responding to issues raised by the project team and planning/implementing appropriate corrective or preventative actions Generating project- or program-level metrics and reports for senior management Capturing lessons learned and contributing to continuous improvement and best practices Required knowledge, skills, and abilities   Bachelor's degree in life sciences or related field   Minimum 4-6 years of experience in project management and/or clinical operations within pharma, CRO, or RWE environment (or equivalent combination of education, training, and experience) Demonstrated experience leading observational or real-world evidence studies Strong understanding of RWE study designs and clinical research conduct and skill in applying applicable clinical research regulatory requirements Experience with primary and secondary data study designs   Therapeutic area expertise desired (oncology) 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 OverviewIQVIA is hiring to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment of a prominent Pharma company. Associate Clinical Project Managers (aCPM) are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The aCPM is a member of the core project team responsible for project delivery of clinical and RWE studies across three therapeutic areas (oncology, virology, inflammation) to meet contractual requirements in accordance with SOPs, policies and practices. The aCPM supports the efforts of the Operations Lead and Project Managers to drive operational excellence and strategic leadership with our customers.Essential Functions Provide input into the development of integrated study management plans with the core project team and/or sub-team. Accountable for assigned portion of clinical studies while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with client standard processes, policies and procedures. Collaborate with other functional groups where necessary to support milestone achievement and to manage study issues and obstacles. Monitor progress and prepare/present project and/or sub-team information proactively to internal stakeholders. Support the project leader to prepare/present project and/or sub-team information proactively to external stakeholders. Identify risk (positive and negative) and contingencies and partner with project leader in problem solving and resolution efforts. Achieve project quality by identifying quality risks and issues, responding to issues raised by project sub-team members and partner with project leader planning/implementing appropriate corrective and preventative action plans. May serve as primary (for small projects) or back-up project contact with customer. Lead the efforts of a project sub-team, responsible for managing cross-collaboration of the sub-team to support milestone achievement and to manage issues and obstacles. Support the project leader in ensuring the financial success of the project. Forecast and identify opportunities to accelerate activities, build best practices, and transition knowledge from clinical to RWE pipeline Identify changes in scope and partner with project leader to manage change control process as necessary. Identify lessons learned and implement best practices. May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements Qualifications Associate's Degree In life sciences or related field required Req Or Bachelor's Degree In life sciences or related field required Req 2 years clinical research experience Req Requires intermediate level knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education combined with experience.; Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge, therapeutic knowledge desired.; Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills. Problem solving - Strong problem solving skills. Organisation - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances. Prioritisation - Ability to handle conflicting priorities. Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output. Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients. Strong customer service skills. Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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

Sales Representative About the Role:We are seeking a motivated and results-driven Pharmaceutical Sales Representative to join our team. In this role, you will be responsible for driving volume and market share growth for assigned pharmaceutical products within a designated territory. You will build strong relationships with healthcare professionals and deliver impactful sales presentations in an office-based setting. Key Responsibilities Include: Generating volume and market share growth for assigned pharmaceutical products within a specific geographic area. Selling presentations to physicians and other health care professionals, primarily in an office-based setting. Developing an understanding of the issues and opportunities unique to the geography, particularly in managed health care. Manage allocated resources (samples, promotional and educational materials) to maximize return within regulatory and ethical guidelines. Maintains accountability for all pharmaceutical samples in accordance with FDA and PDMA guidelines. Utilize the sales automation system to document call and program activity. Complete initial and ongoing product and development training as required.Requirements: BA/BS requiredPreferred: Minimum of 2 years business-to-business outside sales experience with demonstrated record of impact preferred. 1-2 years of Pharmaceutical Sales experience with demonstrated record of impact preferredEstablished relationships within targeted geography.Key Competencies: Sales ability/persuasiveness, use of appropriate interpersonal style and communication methods to facilitate an acceptance of an idea, plan, activity or product from targeted customers.Establishes account plans based on customer needs and business priorities.Establishes method for monitoring progress to goals.Must set high goals or standards of performance, self-starter, able to work independently.Must demonstrate ability to influence events to achieve goals and take actions beyond what is required in being proactive.Must be able to utilize resources and create a positive/professional impression, commanding attention and respect, displaying confidence.Ability to maintain effectiveness in varying environments and with different tasks, responsibilities and people is key.Must express ideas effectively in individual and group situations, adjusting to the characteristics or needs of the target audienceWhether you're educating prescribers, supporting patients, or engaging with physicians, you'll help demonstrate product value and contribute to real-world medical breakthroughs. Explore your potential and help shape a healthier future with IQVIA. LI-CES IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is 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 $90-115,000 annually. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA Digital is hiring a Director, Software Development to lead a core engineering organization responsible for our audience and data platforms. This role owns delivery, technical direction, and operational performance across a distributed team of managers and senior engineers (FTE + contractors). You will drive the architecture and evolution of APIs, data pipelines, and web platforms that power IQVIA Digital’s HCP and audience capabilities—ensuring they scale reliably, integrate cleanly across products, and support the needs of the business. Key Responsibilities Organizational Leadership Lead a team of engineering managers and senior engineers across global teamsDrive consistent engineering practices across design, development, deployment, and operationsOversee staffing, performance management, and vendor/contractor alignmentStrategy & Execution Define and execute technology strategy aligned to IQVIA Digital business prioritiesPartner closely with Product, Data, and Commercial teams to deliver against roadmap commitmentsInfluence senior leadership and drive alignment across cross-functional stakeholdersPlatform & Architecture Ownership Own end-to-end delivery and operation of API platforms connecting Digital products and datasetsOversee engineering for core Audience data assets (HCP, HCN, identity, ingestion pipelines)Ensure scalability, reliability, and performance of data and integration platformsOperational & Delivery Excellence Establish and enforce standard SDLC, release, and operational processes aligned to IQVIA Digital engineering practicesEnsure predictable, high-quality delivery across squads and platformsManage budgets, vendor relationships, and cost efficiencyTalent Development Coach and develop engineering managers and senior technical leadersBuild a strong leadership pipeline and succession plansFoster a culture of accountability, innovation, and continuous improvementQualifications 12+ years in software development, including leadership of large-scale engineering teams8+ years managing engineering managers and/or senior technical leadersProven experience leading global, distributed teams and complex delivery organizationsExperience in product-led organizations with strong collaboration between Engineering and Product ManagementTrack record of aligning technical execution to business outcomesStrong background in: API architecture, development, and integration platformsData engineering and large-scale data platformsCloud-native environments (AWS, Snowflake preferred)Experience incorporating AI-assisted development and modern engineering tooling into the SDLCNice to have: Experience leading web and/or native mobile application development teamsTechnical Expertise (Representative, not exhaustive) API architecture (REST, GraphQL) and system integrationsData engineering & processing (Snowflake, Databricks, Spark)Cloud-native architecture (AWS, Kubernetes, Docker)Backend engineering (Python, Java, Node.js; API and ORM-based data access)Modern application architecture (web and mobile), including Web: JavaScript/TypeScript, React-based frameworks (Next.js), server-side rendering. Mobile: Native (Swift/Kotlin) and cross-platform (React Native) architecturesLegacy system modernization into scalable, web-based platforms (e.g., internal tools, admin platforms)Secure application design (SSO, RBAC, enterprise authentication patterns)CI/CD and developer tooling (GitHub, GitLab)Familiarity with AI-assisted development tools (e.g., Cursor)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 $119,900.00 - $334,200.00. 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.