IQVIA

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• Bachelor's Degree Scientific discipline or health care preferred.• Requires at least 2 years of on-site monitoring experience.• Availability to travel (onsite monitoring) • Living in Mexico City• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.• Good therapeutic and protocol knowledge as provided in company training.• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).• Written and verbal communication skills including good command of English language.• Organizational and problem-solving skills.• Effective time and financial management skills.• Ability to establish and maintain effective working relationships with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewPerform 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• Bachelor's Degree Scientific discipline or health care preferred.• Requires at least 2 years of on-site monitoring experience.• Availability to travel (onsite monitoring) • Location: Mexico City, Guadalajara or Monterrey.• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.• Good therapeutic and protocol knowledge as provided in company training.• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).• Written and verbal communication skills including good command of English language.• Organizational and problem-solving skills.• Effective time and financial management skills.• Ability to establish and maintain effective working relationships with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

We are seeking Product Support Technical Advisor II 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 senior Tier-3 product support for enterprise laboratory applications and integrated systems supporting U.S.-based lab operations. This role drives rapid resolution of high-impact production incidents, delivers onsite technical troubleshooting, and helps maintain continuity across critical workflows such as kit production, sample processing, and study execution. What You'll Be Doing:Provide Tier-3 support for complex, business-critical incidents across production and non-production environmentsLead resolution of high-priority escalations and serve as the escalation point for Tier-2 supportDeliver onsite troubleshooting for lab devices, instruments, printers, iPads, and network-related issuesPerform root cause analysis, document findings, and drive corrective and preventive actionsCoordinate with Development, DBA, Cloud, and vendor teams to restore service and improve system stabilitySupport change and release activities, production validation, and hypercare stabilizationMonitor ticket queues to ensure SLA adherence and timely closure of escalations What We Are Looking For:Bachelor’s degree in computer science or equivalent experience6–10+ years in application/product support with Tier‑3 or senior support experienceStrong technical expertise in Windows, SQL/Oracle, IIS, .NET, Unix/Linux, and Azure/AWSExperience with debugging, log analysis, and advanced production issue resolution across applications, databases, and integrationsOther Equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Strong communication and stakeholder management skills in a fast-paced support environmentExcellent analytical thinking, prioritization, and end-to-end incident ownershipWorking knowledge of ITIL processes including Incident, Problem, and Change ManagementAbility to operate effectively in 24x7 or global support models aligned to U.S. business hoursExposure to scripting, automation, and AI-driven support improvements 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 IQVIA 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 $57,000.00 - $142,700.00. 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.

Position Title: Mobile Medical Assistant / Phlebotomist – Per Diem, In-Home Services    Location: Various U.S. locations (local travel within designated geographic area)    About the Role: IQVIA’s In-Home Clinical Solutions team seeks a qualified and dedicated Mobile Medical Assistant / Phlebotomist to support patient care by delivering in-home diagnostic services. This per diem role involves traveling to patient residences to perform clinical services such as, but not limited to, phlebotomy, electrocardiograms (EKGs), and macular edema screenings in support of treatment initiation and adherence strategies.    This is a per diem, travel-based role offering flexible hours, with no minimum monthly visit requirement. Referrals are assigned based on your geographic availability and program demand. IQVIA manages all scheduling and patient communication, allowing you to focus entirely on clinical care.    Position Details:  Per diem, mobile-based role with flexible scheduling  No minimum monthly visit commitment required  Paid hourly compensation that includes the appointment time and travel time to/from patient’s home. (2 hour minimum paid)  IRS-standard mileage rate reimbursement.    Key Responsibilities:  Perform in-home blood specimen collection, labeling, and transporting specimens according to network policies, procedures, and regulatory standards.  Comply with all laboratory safety and handling procedures; ensure appropriate delivery to designated laboratories.  Conduct screenings as has been appropriately trained to conduct, including but not limited to electrocardiograms (EKGs) and macular edema screening exams (training provided).  Maintain a clean and organized work environment, including transportation and supplies storage specific to the In-Home Network.  Monitor and manage clinical supply inventory.  Collaborate with IQVIA’s clinical coordination team to execute and submit appropriate visit-related paperwork promptly and accurately.   Identify and report adverse events, medical product complaints, or patient inquiries in accordance with IQVIA and manufacturer guidance.  Maintain accurate mileage and time logs for reimbursement and compliance purposes.     Qualifications:  Minimum 2 years of phlebotomy experience in clinical or field settings required  At least 1 year of EKG experience preferred  Certification as a Certified Medical Assistant (CMA) or Phlebotomy Technician (CPT) preferred.  If located in the state of Washington or Louisiana, a state issued CMA or CPT license is required.  Ability to lift up to 70 pounds to transport medical or diagnostic equipment (e.g., eye exam kits).  Ability and willingness to travel up to 100 miles to conduct patient visits.  Proficiency in using medical equipment and upholding proper documentation practices.  Strong interpersonal and communication skills with a patient-focused approach.  Fluent in spoken and written English.  Must possess a valid driver’s license and will be subject to a review of driving record prior to hire.  Must complete a drug screening and background check after accepting an offer.    #LI-CES  #LI-DNP  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is 25.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job Summary Under the direction and supervision of the Director of Clinical Trial Management, this position is responsible for the preparation, scanning, labeling and maintenance of medical records for the practice. The position works closely with the research team in support of all ongoing clinical studies. Essential Duties and Responsibilities Demonstrates an understanding of patient/sponsor confidentiality to protect the patient and practice Creates and maintains the patient medical record for each patient; in electronic format and in paper, as needed. Following HIPAA guidelines gathers patient records from a variety of sources (i.e., mail, fax/eFax, email, etc.), which will require interacting with registration areas and/or physicians' office's in a professional manner. Scans and attaches medical records into the electronic medical record system according to guidelines. Keeps practice health care providers informed by communicating availability or unavailability of the record. Handles medical record requests and patient care related releases of information ensuring that all releases are compliant with HIPAA guidelines. Assists in purging deceased and inactive charts as scheduled and according to guidelines. Ability to assist in the guidance and training of less experienced staff. • Ability to maintain a positive attitude with the research team. Remains current with all required Knowledge, Skills & and Abilities Excellent interpersonal skills to deal effectively with research personnel Knowledge of medical terminology. Knowledge of HIPAA guidelines. Excellent organizational skills to independently manage workflow. Ability to prioritize quickly and appropriately with minimal guidance. Ability to multi-task. Ability to work independently and function as part of a team. Clear and concise verbal and written communications. Excellent attention to detail. High school graduate or GED Why Join Us? At NEXT Oncology (an Avacare Business), you’ll be part of a mission-driven team that values collaboration, precision, and patient safety. Our team is known for its supportive culture, strong communication, and commitment to excellence in clinical research. 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 $25,900.00 - $64,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. Our mission is to accelerate the development and commercialization of medical treatments that improve patient outcomes and population health worldwide. With more than 88,000 employees globally, IQVIA combines advanced analytics, technology solutions, scientific expertise, and deep healthcare knowledge to help bring innovative therapies to patients faster. As a Project Manager within IQVIA's Patient Centered Solutions team, you will play a pivotal role in leading the successful delivery of a growing portfolio of patient-focused clinical research and implementation science projects. Supporting an expanding in-trial interview program, you will oversee a portfolio of complex studies, providing strategic project leadership from initiation through closeout. You will be accountable for ensuring quality, timelines, budgets, and stakeholder expectations are consistently met while serving as the primary point of contact for sponsors. Working closely with cross-functional teams, you will drive operational excellence, champion the patient perspective, and contribute to research that shapes treatment development and healthcare outcomes. Key Responsibilities Lead the successful execution of studies from initiation through closeout, ensuring delivery against scope, timelines, budget, and quality objectives Serve as the primary point of contact for sponsors, building strong client relationships and ensuring exceptional customer satisfaction Develop and maintain integrated project management plans and coordinate activities across cross-functional teams Supervise and mentor Clinical Project Coordinators and Analysts, supporting team development and performance Monitor project progress and communicate study status, key metrics, risks, and mitigation plans to internal and external stakeholders Identify, assess, and proactively manage project risks, issues, and dependencies, driving timely resolution and corrective actions. Ensure compliance with applicable SOPs, policies, processes, and quality standards Manage project budgets, forecasting, and financial performance to ensure efficient project delivery Partner with internal functions and external vendors to support study milestones and operational success Support resource planning activities to ensure projects are appropriately staffed and aligned to business needs Contribute to continuous improvement initiatives, lessons learned activities, and best-practice sharing across the organization Qualifications & Experience Bachelor's degree in Life Sciences, Healthcare, Public Health, Psychology, or another related scientific discipline 5–8 years of project management experience within clinical research, patient-centered research, implementation science, healthcare, CRO, pharmaceutical, or biotechnology environments Proven experience managing complex studies or portfolios involving multiple stakeholders and workstreams Strong understanding of clinical research methodologies and applicable research regulations, including ICH-GCP principles Demonstrated experience managing project budgets, forecasting, and financial performance Excellent leadership skills with the ability to effectively manage and motivate cross-functional teams Strong risk management, problem-solving, and decision-making capabilities Outstanding communication, presentation, and stakeholder management skills Ability to work effectively across global teams and diverse cultural environments Advanced proficiency in Microsoft Office applications, including Excel, PowerPoint, and Word Fluency in English is required 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.

Pharma Data Panel – Intern We are looking for an Intern to work in our Pharma Data Panel team that wants to develop analytical, organizational and commercial skills. Activities: ·       Engage with pharmacy professionals and build and maintain a solid relationship ·        Data management and data analysis ·        Promote and support pharmacy services portfolio by giving online training to the pharmacies about pharmacy management and marketing tools, based in our data. ·        Performing quantitative and qualitative analysis to proactively better understand the panel data and then turning data into valuable information. ·        Contributing to internal and external brainstorming sessions to develop new ideas and methodologies. Requirements: ·        Bachelor’s degree on Pharmaceutical Sciences ·        High knowledge of the office package, mainly Excel and PowerPoint. ·        Exceptional analytical and quantitative problem-solving skills. ·        Ability to work collaboratively with different stakeholders (internal and external) ·        Well-developed written and verbal communication skills including presentations. ·        Strong capability in juggling priorities to meet deadlines. ·        High English level and Native Spanish What we offer• Participation in innovative projects.• A rich learning environment with exposure to real world data, client interactions, and improvement initiatives.• Opportunities to develop analytical, operational, and technical skills.• A positive, collaborative work environment.• An internship experience designed to support your professional and personal growth. Location: Madrid or Barcelona Hybrid Formula 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.

🔹 ¡Únete a uno de los proyectos más sólidos y exitosos del sector! 🔹Seleccionamos Delegad@ de Clínicas Dentales, y Venta en Farmacia con base en Málaga, para incorporarse a un proyecto consolidado y de gran proyección a nivel nacional.📍 Zona de trabajo: Málaga y Granada.Buscamos una persona con excelentes habilidades de comunicación, marcada orientación al cliente, iniciativa y proactividad, capacidad de análisis y planificación, así como ganas de aprender, crecer y desarrollar una carrera profesional en la Industria Farmacéutica. Si te identificas, ¡esta es tu oportunidad!🧩 Responsabilidades:-Realizar la visita comercial y promocional dentro de la zona asignada.-Contribuir activamente al plan de negocio nacional, asegurando el cumplimiento de objetivos.-Desarrollar una promoción eficaz entre los distintos profesionales de la salud.-Adoptar un enfoque global del negocio, trabajando con un alto nivel de autonomía y responsabilidad.💼 ¿Qué te ofrecemos?Formar parte de un proyecto estable, con un entorno dinámico, aprendizaje continuo y oportunidades reales de desarrollo profesional.¿Te interesa? 🚀 ¡Queremos conocerte! Ventajas sociales o económicasTodas las herramientas de trabajo incluidas.Acceso a plan de retribución flexible y formación.Otros requisitos- Deseable Diplomado o estudios Universitarios.- Altamente valorable poseer formación en Ciencias de la Salud.- Experiencia previa comercial de al menos 6 meses.- Valorable conocimiento del sector farmacéutico.- Buen manejo y uso de tecnologías IT.- Disponer de carnet de conducir.Competencias y habilidades:-Excelentes habilidades de comunicación.-Cultura de servicio al cliente.-Iniciativa, proactividad.-Capacidad de análisis, organización y planificación.-Ganas de aprender, mejorar y desarrollar una carrera profesional en la Industria Farmacéutica.-Motivación por el trabajo comercial y las relaciones interpersonales.#LI-CES #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

¿Te apasiona la nutrición clínica y quieres marcar un impacto real en la calidad de vida de las personas?¡Esta es tu oportunidad para unirte a un proyecto innovador, sólido y con propósito! 🚀 Buscamos un/a Nutriasesor/a para liderar el servicio de asesoramiento nutricional en residencias y hospitales. La posición tiene base en Valencia y el área de trabajo será la Comunidad Valenciana.🔍 ¿Qué buscamos?✅ Excelentes habilidades de comunicación y trato humano. ✅ Empatía, orientación al residente y cultura de servicio. ✅ Organización, planificación y autonomía. ✅ Capacidad de adaptación a distintos centros y equipos. ✅ Iniciativa, proactividad y orientación a resultados.🎯 Tu misión:• Realizar screening nutricional con herramientas digitales y valoración clínica.• Elaborar informes nutricionales individualizados y planes de intervención adaptados a cada residente.• Realizar seguimiento nutricional continuado según nivel de riesgo y tipología del centro.• Asegurar la correcta aplicación de los protocolos nutricionales definidos, garantizando trazabilidad y calidad asistencial.• Impartir formaciones presenciales y online a los profesionales de los centros.• Ofrecer soporte técnico-científico continuo a través de los canales establecidos.• Asesorar en menús y dietas personalizadas, aportando recomendaciones cualitativas y documentación estándar.• Colaborar con equipos multidisciplinares para asegurar la correcta implementación de las recomendaciones nutricionales.• Gestionar y mantener la información clínica y nutricional, asegurando calidad de datos y reportes.• Participar en estudios y proyectos científicos cuando aplique.• Contribuir a la gestión de la calidad del servicio (indicadores, auditorías internas, no conformidades).✨ ¿Qué ofrecemos? 💼 Proyecto estable, con propósito y en crecimiento. 📚 Formación continua y acceso a congresos especializados. 🤝 Entorno colaborativo con profesionales líderes en nutrición clínica. 🚀 Plan de carrera y desarrollo profesional. 💳 Acceso a plan de retribución flexible.Si buscas un reto profesional que combine especialización, autonomía y proyección, ¡Envíanos tu candidatura y únete a nuestro equipo! 💪 #LI-CES #LI-DNI IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. 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.

Position Title: Mobile Nurse (LPN/LVN) – Per Diem, In-Home Services    Location: Various U.S. locations (local travel within designated geographic area)    About the Role: IQVIA’s In-Home Clinical Solutions team seeks a qualified and dedicated Mobile Licensed Practical Nurse (LPN) or Licensed Vocational Nurse (LVN) to deliver in-home clinical services to patients initiating therapy with complex medications. This per diem role involves traveling to patient residences to perform clinical services such as, but not limited to, phlebotomy, electrocardiograms (EKGs), and macular edema screenings in support of treatment initiation and adherence strategies.    This is a per diem, travel-based role offering flexible hours, with no minimum monthly visit requirement. Referrals are assigned based on your geographic availability and program demand. IQVIA manages all scheduling and patient communication, allowing you to focus entirely on clinical care.     Position Details:  Per diem, mobile-based role with flexible scheduling  No minimum monthly visit commitment required  Paid hourly compensation that includes the appointment time and travel time to/from patient’s home. (2 hour minimum paid)  IRS-standard mileage rate reimbursement.    Key Responsibilities:  Perform in-home blood specimen collection, labeling, and transporting specimens according to network policies, procedures, and regulatory standards.  Comply with all laboratory safety and handling procedures; ensure appropriate delivery to designated laboratories.  Conduct screenings as has been appropriately trained to conduct, including but not limited to electrocardiograms (EKGs) and macular edema screening exams (training provided).  Maintain a clean and organized work environment, including transportation and supplies storage specific to the In-Home Network.  Monitor and manage clinical supply inventory.  Collaborate with IQVIA’s clinical coordination team to execute and submit appropriate visit-related paperwork promptly and accurately.   Identify and report adverse events, medical product complaints, or patient inquiries in accordance with IQVIA and manufacturer guidance.  Maintain accurate mileage and time logs for reimbursement and compliance purposes.    Qualifications:  Active and unrestricted LPN or LVN license required  Current CPR certification required  Minimum 2 years of phlebotomy experience in clinical or field settings required  At least 1 year of EKG experience preferred  Certification as a Certified Medical Assistant (CMA) or Phlebotomy Technician (CPT) preferred.  Ability to lift up to 70 pounds to transport medical or diagnostic equipment (e.g., eye exam kits).  Ability and willingness to travel up to 100 miles to conduct patient visits.  Proficiency in using medical equipment and upholding proper documentation practices.  Strong interpersonal and communication skills with a patient-focused approach.  Fluent in spoken and written English.  Must possess a valid driver’s license and will be subject to a review of driving record prior to hire.  Must complete a drug screening and background check after accepting an offer.    #LI-CES  #LI-DNP  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is 28.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human ingenuity to drive healthcare forward. Job OverviewSpecialist sales role  will be responsible for leading, facilitating and supporting with all Regulatory Insights activity for EMEA.  Working closely with the country teams, this role will support the teams to develop new, and manage and expand, existing business within the region, support in large engagements, input into the planning and forecasting process as well as managing and developing opportunities. Essential Functions• Develop and execute on a clear sales plan, aligned to country, to achieve the objectives for Regulatory Intelligence for EMEA• Achieves growth & revenue targets • Understand risks and opportunities to plan for achieving overall• Support the countries with monthly forecasting and annual planning cycles• Client Solution creation and alignment in region and globally• Direct involvement in contract renewals and negotiations as required• Managing the teams both directly and indirectly and leading performance management, development and learning discussions with direct reports• Reporting on an ongoing basis on the above to Sales Director and for corporate reporting such as Functional Reviews• As necessary, identifies and manages resources to develop proposals that position IQVIA capabilities & solutions to customers• Gathers market and client intelligence and provides strategic feedback to Marketing, Consulting, Service, and Sales to strengthen or product offerings and capture additional business Qualifications - our ideal candidate will have• Bachelor's Degree or equivalent • 5 years strong sales and account management experience• Demonstrable experience of sales growth & target achievement• Strong examples of consultative sales approach solving client business issues• Possesses knowledge of key marketplace issues for the pharmaceutical industry and related businesses• Excellent presentation and writing skills• Must have successful experience identifying and closing new business opportunities & be results driven• Developing positive relationships at all levels of client management and within the IQVIA sales, consulting and marketing teams APPLICANTS MUST HAVE THE RIGHT TO WORK IN THE UK AS THIS ROLE IS NOT OPEN TO VISA SPONSORSHIP We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The Part Time Clinical Consultant (PTCC) role is an exciting opportunity to join IQVIA.  IQVIA/MedTech takes the approach to helping customers drive healthcare forward in this challenging, fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities. This part time position will be responsible for providing case support, patient management, and education to both new and existing accounts within an assigned client Franchise/Region.  Duties and Responsibilities: Acquire and demonstrate a working knowledge of our products/therapies and develop an understanding of their applications.Improve patient outcomes by delivering ventricular medical device education in a variety of settings, including but not limited to, the ICU, OR, and Cath Lab.Ventricular medical device case support, including on call support.Complete proactive rounds for patients receiving support and provide assistance.Collaborate with the Clinical Support Center (CSC) for ongoing additional support as necessaryMaintain clinical competency in current product line, patient management, and remain up to date on most relevant information through continual learning and educationSome travel may be neededJob Qualifications: Clinical certification required; Registered Nurse (RN)/Advanced Practice Provider (APP) license strongly preferred.3+ years’ experience with a strong clinical background in the Cardiac ICU (CICU), Cardiovascular ICU (CVICU), Cardiovascular OR (CVOR), or Catheterization Lab (Cath Lab) required; CVICU experience highly preferred.Some industry experience preferred, but not required.Significant experience with ventricular medical device is required (minimum of 10 cases/patients supported).Must provide a minimum of (2) days of live support within the field (case support, patient rounding, providing education), with a total of (5) days of availability per month.Availability must include (1) weekend per month.Ability to work on weekends, nights, holidays as well as weekdays.Ability to work at other hospitals aside from base location. Ability to clear hospital vendor credentialing requirements.Position may/will require up to date immunizations.#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 $60.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Role overview In this role within the EMEA RW MEG you will be producing materials and services relating to the Health Economics Outcomes Research business areas (health economic modelling, evidence synthesis, statistical analysis, health technology assessment submissions, report and publication development for value communication) that generate value for our clients. The successful candidate: Will be involved in shaping and leading the team and offerings, working closely with the EMEA RWS Center of Excellence for Systematic Literature Review and the wider senior leadership team Has a good understanding of systematic literature methods (e.g., Cochrane) Can independently develop searches in various databases (e.g., EMBASE, MEDLINE, Cochrane, PubMed, etc.) and proficient in using OVID SP or another similar platform Keeps up to date on new methodologies and HTAs requirements for systematic literature reviews and be an in-house go-to expert for the team Has a good understand of different types of literature reviews (e.g., systematic, targeted, pragmatic, etc.) Manages literature review projects with senior oversight Guides the team on interpretation/qualitative synthesis of the literature review findings Oversees literature review projects that meet rigorous HTA requirements, conducts quality control of literature review deliverables (searches, screening files, extractions, reporting) Is a day-to-day contact with clients who will include pharmaceutical, biotechnology and medical devices companies with global and regional headquarters based in the EMEA region, and occasionally their affiliate teams, with senior oversight Oversees the development of research questions, PICOS criteria, search strategies and literature review protocols Contributes to business development as well as internal initiatives for the advancement of innovative methodological approaches Collaborates with other business areas and functions of the organisation to deliver client services and support the development of new offerings Qualifications and desired experience We are looking for a candidate with a good mix of academic and professional experience, domain experience and interpersonal skills. An ideal candidate has a good knowledge of literature review methods and has experience in conducting rigorous literature reviews in health sciences. Desired skills and qualifications: Postgraduate degree level education or higher from a relevant discipline such as health or bioscience-related, medicine, biomedical sciences, health economics, health policy, epidemiology, public health, or information science Prior relevant experience, >2 years (such as, but not limited to experience in systematic literature reviews and/or meta-analyses) Understanding of research principles, PRISMA principles, Cochrane guideline for SLRs, methods of the assessment of risk of bias for different study designs Understanding of the principles of evidence-based healthcare, critical appraisal and the interpretation and synthesis of health care research Understanding (and experience is advantageous) with the HTA agency requirements for evidence reviews and synthesis Excellent oral and written communication skills Accuracy, attention to detail and time management skills An understanding of meta-analysis methods is advantageous, but not essential Strong written and verbal communication skills with fluency in English Demonstrable commercial awareness and thorough understanding of the pharmaceutical industry is advantageous Proficiency in MS Word, PowerPoint, Excel *Resume/CV must be submitted in English* #home-based #remote IQVIA is committed to embracing a diverse and inclusive work environment. Our goal is to attract and retain the best people, regardless of their gender, race, marital status, ethnic origin, national origin, age, disability, sexual orientation, gender identity or any other characteristic. Join us! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewTo support Statistical Team Lead on the following activities1. Statistical Analysis Plan Development2. Programming specification development3. Supporting programming activities 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.

 Attaché de recherche clinique II IQVIA est à la recherche d'un ARC II expérimenté en surveillance d'essais cliniques en oncologie. Ce poste, basé à domicile dans l'est du Canada, nécessite la maîtrise du français et de l'anglais. Aperçu du poste L'ARC II est responsable de la surveillance des essais cliniques de phase I à IV afin d'assurer la conformité aux protocoles, aux BPC/ICH et aux exigences réglementaires. Elle gère les activités des sites, du début à la clôture.Principales responsabilitésEffectuer les visites de sélection, d'initiation, de suivi et de clôture des sitesFormer le personnel des sites aux protocoles d'étude, aux systèmes EDC et aux exigences de l'étudeAssurer la qualité de la documentation source, l'intégrité des données et la résolution rapide des requêtesSuperviser la responsabilité des enquêteurs et la collecte des documents réglementairesÊtre l'interlocuteur principal du site et maintenir une communication régulièrePréparer les rapports de suivi conformément aux procédures opérationnelles standard (SOP) et aux échéanciersSoutenir les réunions des enquêteurs et collaborer avec les coordonnateurs principaux d'étude/ARCDiplômes et expérience Bilingue français-anglais (obligatoire)Baccalauréat requis. De préférence en sciences de la vie ou dans une discipline connexeUne combinaison équivalente de formation et d'expérience peut être acceptée au lieu du diplômeAu moins 1 an d'expérience en suivi sur place (requis)Disponibilité pour des déplacements à hauteur de 65 à 70 %Clinical Research Associate II IQVIA is seeking an experienced Clinical Research Associate II (CRA II) with oncology monitoring experience. This role is home‑based in Eastern Canada and requires fluency in both French and English. Overview The CRA II is responsible for monitoring Phase I–IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. You will manage site activities from start-up through close-out. Key Responsibilities Conduct site selection, initiation, monitoring, and close-out visitsTrain site personnel on study protocols, EDC systems, and study requirementsEnsure high-quality source documentation, data integrity, and timely query resolutionOversee IP accountability and regulatory document collectionServe as the primary site contact and maintain regular communicationPrepare monitoring reports following Standard Operating Procedures and timelinesSupport investigator meetings and collaborate with CTMs/Lead CRAsQualifications Bilingual in French and English (Required).Bachelor’s Degree required. Preference in life sciences or related discipline.  Equivalent combination of education, training and experience may be accepted in lieu of degree.At least 1 year of onsite monitoring experience (Required)Ability to travel 65–70%IQVIA est un fournisseur mondial de premier plan de services de recherche clinique, d'informations commerciales et de renseignements sur les soins de santé pour les secteurs des sciences de la vie et de la santé.  IQVIA se consacre à accélérer le développement et la commercialisation de traitements médicaux innovants pour aider à améliorer les résultats des patients et la santé de la population dans le monde entier. Pour en savoir plus, visitez https://jobs.iqvia.com   IQVIA est fière d’être un employeur souscrivant au principe de l’égalité d’accès à l’emploi. Tous les candidats qualifiés seront pris en considération pour un emploi sans égard à la race, la couleur, la religion, le sexe, l’orientation sexuelle, l’identité de genre, l’origine nationale, le handicap, l’âge, l’état matrimonial ou tout autre statut protégé par la loi applicable.  Des mesures d’adaptation pour les candidats handicapés sont disponibles sur demande dans tous les aspects du processus de recrutement. Si vous avez un handicap qui nécessite une mesure d’adaptation, nous vous encourageons à contacter notre équipe d’acquisition de talents au [email protected], afin qu’IQVIA puisse soutenir votre participation au processus de recrutement. IQVIA s’engage à faire preuve d’intégrité dans son processus de recrutement et applique une politique de tolérance zéro en matière de fraude des candidats. Toutes les informations et toutes les qualifications soumises dans votre candidature doivent être véridiques et complètes. Toute fausse déclaration, présentation trompeuse ou omission importante au cours du processus de recrutement entraînera la disqualification immédiate de votre candidature, ou la cessation d’emploi si elle est découverte ultérieurement, conformément aux lois applicables. Nous apprécions votre honnêteté et votre professionnalisme. Veuillez noter qu'il est possible que nous utilisions l'intelligence artificielle (IA) dans le traitement de votre candidature. Cependant, nous utilisons l'IA uniquement pour aider notre équipe de recrutement à sélectionner ou à évaluer les candidatures, et non pas pour remplacer la prise des décisions par les membres de notre équipe. 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, age, marital status, or any other status protected by applicable law.  Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. If you have a disability that requires an accommodation, we encourage you to contact our Talent Acquisition Team at: [email protected], so that IQVIA can support your participation in the recruitment process. 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. Please note that we may use artificial intelligence (AI) in the processing of your application. However, we only use AI to assist our recruitment team with the screening or assessment of candidacies, and not as a substitute for human decision-making. La fourchette salariale de base potentielle pour ce poste, annualisée, est de $84,000.00 - $170,900.00. Le salaire de base réel offert peut varier selon plusieurs facteurs, notamment les qualifications liées à l’emploi telles que les connaissances, les compétences, la formation et l’expérience; l’emplacement; et/ou l’horaire (temps plein ou temps partiel). Selon le poste offert, des régimes d’incitation, des primes et/ou d’autres formes de rémunération peuvent être proposés, en plus d’une gamme d’avantages sociaux liés à la santé, au bien-être et/ou d’autres bénéfices.  The potential base pay range for this role, when annualized, is $84,000.00 - $170,900.00. 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 wellness and/or other benefits.

Location: Gujranwala Job OverviewUnder guidance, oversees the day to day operations of a team of Data Collectors in the field.Essential Functions• Recruit physicians and other primary healthcare professionals to collect primary data.• Build long term relationships with physicians and other primary healthcare professionals.• Complete administrative tasks related to data collection such as time management, reporting etc.• Provide support and guidance on existing projects and studies for more junior staff, and provide coaching for more junior staff in their roles.• Act as an “ambassador” for the company to external contacts including physicians and other stakeholders• Act as the main point of contact internally for physician and healthcare professional queries• Monitor key metrics for quality, speed and efficiency to drive internal and external client satisfaction. Qualifications • Graduate degree or equivalent. • Minimum 3 years of experience in Sales, preferably in Pharmaceutical companies. •Strong relationship-building skills with healthcare professionals. •Good analytical and problem-solving abilities. •Willing to travel as required for the role 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.

Make an impact on patient health!  IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes.   We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers.   IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication.   We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available.  Job OverviewUnder supervision, executes the regulatory and  maintenance activities in accordance with regulations, SOPs, and project requirements at country level.Job Responsbilities Work with Maintenance Specialists closely for  preparation & submission & shipment of Maintenance MOH, EC submission, and also CTA folder preparation and shipment.Review documents for completeness, consistency and accuracy, under guidance of senior staff.Prepare site submission documents, reviewing for completeness and accuracy.Inform team members of completion of regulatory contractual. and other documents for individual sites.Distribute completed documents to sites and internal project team members.Update and maintain internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.Review, track and follow up the progress, the approval and execution of required documents , regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.Qualifications Bachelor's Degree Pursuing degree ReqAppropriate verbal and written communication skills to function within a professional work environment.Evidence of effective problem – solving, analytical, and critical thinking skills.Proficiency in alignment with the desired role placementEvidence of strong team work and communication skills. Join IQVIA and let’s create a healthier world together:  Exposure across 21 Therapeutic Areas  Be part of a global team who operate across 141 locations  Exposure across a variety of studies and projects  Access to new, innovative technologies  Work within a collaborative and vibrant environment  Own your career!  Unleash your potential!  It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world.  When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.  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 Summary The Phlebotomist will obtain and prepare specimens for analysis and perform various screening tests. Provide basic medical care to patients under the supervision of RNs/Physicians. Advocates for patient safety and protocol integrity, adheres to standards, and communicates effectively to ensure effective conduct of clinical trials and quality patient care.  Essential Duties and Responsibilities Essential and other important responsibilities and duties may include but are not limited to the following: Obtains, and documents vital signs to include pulse, blood pressure, temperature, respiratory rate, height, and weight Confirms and documents fasting status Obtains and documents pain scale and fatigue scale Obtains clinical labs and study specific specimens according to the patients schedule and protocol guidelines Obtains good quality ECGs according to the patients schedule and protocol guidelines Assists RNs/Physicians with procedures or examinations Prepares laboratory requisitions and supplies Maintains cleanliness of draw stations and work areas Inventories and requests supplies as necessary Other duties as assigned Required Education and Experience High school diploma or equivalent Current BLS required MA certification OR Phlebotomy certification required Previous experience in a health-related field preferred Why Join Us? At NEXT Oncology (an Avacare Business), you’ll be part of a mission-driven team that values collaboration, precision, and patient safety. Our team is known for its supportive culture, strong communication, and commitment to excellence in clinical research. 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 $26,900.00 - $67,100.00. 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.

The NEXT Oncology team is hiring a licensed IDS Pharmacy Technician to join our well-rounded, cohesive, and supportive team focused on Phase I, Oncology trials. This role offers a steady Monday–Friday schedule with daytime hours, making it ideal for professionals seeking work-life balance while contributing to cutting-edge cancer research. You’ll have the opportunity to apply your pharmacy technician expertise in both hands-on compounding and administrative support, gaining exposure to a wide range of responsibilities that promote continuous learning and professional growth. Key ResponsibilitiesProtocol Compliance: Enter concomitant medications into EMR and prepare investigational products per protocol. Medication Preparation: Compound IV and oral investigational and conventional agents, including hazardous medications, with precision and adherence to USP and . Inventory & Accountability: Manage IP and conventional drug inventory, supplies, and documentation in Vestigo and eDOCs. Administrative Support: Assist with audits, monitor visits, and SOP development; provide coverage for team members as needed. Education & Training: Orient new staff and maintain required certifications and continuing education. Data & Documentation: Upload and manage protocol and credential documentation using eDOCs and Vestigo. Minimum QualificationsCurrent Pharmacy Technician License in Texas (Required) IV Certification with at least 1 year of mixing experience (preferred) Chemotherapy Certification with at least 6 months of mixing experience (preferred) Strong knowledge of USP , USP , GCP, GMP, and oncology research practices Ability to lift up to 40 lbs and stand/walk for extended periods Why Join Us?At NEXT Oncology, you’ll be part of a mission-driven team that values collaboration, precision, and patient safety. Our IDS team is known for its supportive culture, strong communication, and commitment to excellence in clinical research. 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 $33,000.00 - $82,600.00. 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.

Position Title: Mobile Medical Assistant / Phlebotomist – Per Diem, In-Home Services    Location: Various U.S. locations (local travel within designated geographic area)    About the Role: IQVIA’s In-Home Clinical Solutions team seeks a qualified and dedicated Mobile Medical Assistant / Phlebotomist to support patient care by delivering in-home diagnostic services. This per diem role involves traveling to patient residences to perform clinical services such as, but not limited to, phlebotomy, electrocardiograms (EKGs), and macular edema screenings in support of treatment initiation and adherence strategies.    This is a per diem, travel-based role offering flexible hours, with no minimum monthly visit requirement. Referrals are assigned based on your geographic availability and program demand. IQVIA manages all scheduling and patient communication, allowing you to focus entirely on clinical care.    Position Details:  Per diem, mobile-based role with flexible scheduling  No minimum monthly visit commitment required  Paid hourly compensation that includes the appointment time and travel time to/from patient’s home. (2 hour minimum paid)  IRS-standard mileage rate reimbursement.    Key Responsibilities:  Perform in-home blood specimen collection, labeling, and transporting specimens according to network policies, procedures, and regulatory standards.  Comply with all laboratory safety and handling procedures; ensure appropriate delivery to designated laboratories.  Conduct screenings as has been appropriately trained to conduct, including but not limited to electrocardiograms (EKGs) and macular edema screening exams (training provided).  Maintain a clean and organized work environment, including transportation and supplies storage specific to the In-Home Network.  Monitor and manage clinical supply inventory.  Collaborate with IQVIA’s clinical coordination team to execute and submit appropriate visit-related paperwork promptly and accurately.   Identify and report adverse events, medical product complaints, or patient inquiries in accordance with IQVIA and manufacturer guidance.  Maintain accurate mileage and time logs for reimbursement and compliance purposes.     Qualifications:  Minimum 2 years of phlebotomy experience in clinical or field settings required  At least 1 year of EKG experience preferred  Certification as a Certified Medical Assistant (CMA) or Phlebotomy Technician (CPT) preferred.  If located in the state of Washington or Louisiana, a state issued CMA or CPT license is required.  Ability to lift up to 70 pounds to transport medical or diagnostic equipment (e.g., eye exam kits).  Ability and willingness to travel up to 100 miles to conduct patient visits.  Proficiency in using medical equipment and upholding proper documentation practices.  Strong interpersonal and communication skills with a patient-focused approach.  Fluent in spoken and written English.  Must possess a valid driver’s license and will be subject to a review of driving record prior to hire.  Must complete a drug screening and background check after accepting an offer.    #LI-CES  #LI-DNP  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is 25.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job Description: •    Produce materials and services relating to the Health Economics and HTA business areas (health economic modelling, evidence synthesis, statistical analysis, health technology assessment submissions, report and publication development for value communication) that generate value for our clients  •    Engage with large data sets and apply real-world data to health economic decision-support tools •    Develop your project management skills through client liaison and collaboration with senior project managers •    Contribute to business development as well as internal initiatives for the advancement of innovative methodological approaches •    Work closely with a diverse range of peers, project managers and subject matter experts, both in the London office and offices across the world  Who you are: •    You have a degree in science, economics, mathematics, statistics, computer science or another relevant discipline •    You have strong numeracy and quantitative skills as well as competency using MS Excel and statistical packages (e.g. Stata, R, SAS) •    You are capable of tackling loosely defined problems analytically and applying pragmatic and logical problem solving skills •    You are a communicative person that values building strong relationships with colleagues and clients and have the ability to explain complex topics in simple terms and in a structured way, both spoken and written IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Title: Registered Dietician - FloridaLocation: Remote in United States Job Type: Per Diem IQVIA are looking for experienced Dieticians to join our team. The ideal candidate will have experience in providing dietary advice and support to individuals with rare diseases. Key Responsibilities: Our remote Registered Dieticians are responsible for: Conduct nutritional assessments and develop personalized dietetic plans for clients with various disease classifications via telecommunications. Provide ongoing dietetic counselling and support to clients and their familiesNutritional assessments and dietetic counseling (only done for clients in which you are licensed to practice.) Maintain accurate and confidential client recordsParticipate in virtual team meetings and training sessionsQualifications: Qualified Registered Dietician (CDR) with Current National Registration In State Licensure: Unencumbered and active state license (except if in CA, MI, NJ, AZ, VA, CO)Minimum 1 year of experience working experience in planning for and coaching patients Minimum 1 year of experience working remotely via telehealthExcellent communication and interpersonal skillsExperience working with patients with obesity (with and without diabetes) preferredExperience managing patients on GLP-1 preferredBilingual (Spanish/English) is required.Note: This position is not eligible for sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is 45 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job OverviewUnder close guidance or supervision, Acquires data from suppliers and formats it into a form that can be input into IQVIA systems. Essential Functions• Receives, identifies, and logs all inbound data from suppliers.• Replenishes blank media to data suppliers as required.• Executes the movement of data through IQVIA acquisition platforms according to standard operating procedures.• Performs initial volume checks to determine whether the amount of data received is realistic. Qualifications • Japanese can be working language• Knowledge of PC-based Windows applications, mainframe tools as used by IQVIA and third-party tools and software• Good interpersonal and communications skills essential.• Ability to work in a team environment, to follow directions accurately and to work under time constraints and changing work volumes.• Ability to follow established procedures to resolve routine matters.• Understanding of the workflow and processes for the different audits. 在公司的标准流程指导下，负责收集供应商数据，并进行数据整理和格式转换，确保数据符合 IQVIA 系统录入要求。 岗位职责 接收、识别并登记所有来自数据供应商的输入数据。根据需要向数据供应商补充和提供空白数据介质。按照标准操作流程（SOP）执行数据在 IQVIA 数据采集平台中的流转和处理。对接收的数据进行初步数据量检查，确认数据规模的合理性。 任职要求日语可以作为工作语言具备基础的系统和业务流程知识。熟悉 Windows 办公软件及相关数据处理工具。具备良好的沟通协调和人际交往能力。具有团队合作精神，能够在时效要求和工作量变化环境下开展工作。能够按照既定流程独立处理日常事务和常规问题。了解数据审核及相关业务工作流程。 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 Healthcare Collection Associate will be responsible 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 Monday thru Friday - No evenings/No Weekends 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 as required 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. Per Diem and flexible availability 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 Position may/will require up to date immunizations.  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, and your time traveling 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: Due to the nature of this role, it is not eligible for Visa sponsorship. #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is $25-$27 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job Overview Provides administrative and/or technical support. Recruitment Process 第一轮：线上测评 完成指定的线上测试，用于初步筛选。 第二轮：业务面试 与业务部门进行面谈，深入了解您的专业背景与职位匹配度。 第三轮：结果通知 招聘团队将在流程结束后，正式告知最终结果。  Essential Functions• Responsible to reconcile SAP Grant Payment Report to Excel Grant Payment Report for assigned Sponsors’ studies, as well as reconcile the total GPS Sponsor balance to the Corporate Sponsor Balance on a monthly basis per SSAE16 Controls• Responsible to accurately complete all necessary journal entries as assign• Responsible to quality review CTA and Payment Intake form setups to determine appropriate SAP vendor and payment method for Payments staff for assigned Sponsor’s studies, inclusive of bank entry validation for the Accounting dept.• Responsible for SharePoint tracker completion for assigned sponsors.• On an annual basis, assist with 1099 and other country tax reporting as assigned• Special projects involving maintenance of the vendor database in SAP, and SOP Maintenance, as required• Other duties as assigned Qualifications• Bachelor's Degree Pursuing degree• Appropriate verbal and written communication skills to function within a professional work environment.• Evidence of effective problem – solving, analytical, and critical thinking skills.• Proficiency in alignment with the desired role placement• Evidence of strong team work and communication skills. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is 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.