IQVIA

We are seeking Senior Scientist - Translational Science Lab (Flow) to join IQVIA Laboratories at Valencia, CA.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary:The Senior Scientist - Translational Science Lab (Flow) is responsible for developing and optimizing moderately complex assays and methods to support timely and effective laboratory delivery. This role also provides technical leadership across troubleshooting, method transfer, and cross-functional collaboration to support scalable laboratory operations. What You'll Be Doing:Plan assay and method development activities and draft clear, robust laboratory methodsExecute method development experiments and support validation and analytical testing activities as neededTroubleshoot assays and apply root cause analysis to optimize performance and resolve technical issuesTransfer methods into validation processes and collaborate across functions to ensure methods are sustainable and scalableLead low to moderately complex technical projects and guide assigned team members to achieve project deliverablesMentor and train junior staff while contributing technical expertise to scientific reports, presentations, and documentationSupport laboratory equipment maintenance, operational standards, and evaluation of new instrumentation What We Are Looking For:Bachelor's degree in a relevant scientific discipline is required4 years of related experience in method or assay development or specific methodology area.Sound knowledge of assay/method development and scientific principles, theories, concepts, and state of the art instrumentationExperience with method validation, assay troubleshooting, and transfer of methods into laboratory operationsOther Equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Strong troubleshooting and advanced problem-solving skills, including application of root cause analysisEffective communication and presentation skills with the ability to work successfully across functionsStrong organizational skills and close attention to detail in a regulated laboratory environmentAbility to manage multiple tasks independently and bring projects to completion within timeline expectationsAbility to establish and maintain effective working relationships with coworkers, managers, and clients What We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.To learn more about our benefits, visit https://jobs.iqvia.com/benefits.If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $64,200.00 - $133,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

We are seeking Senior Scientist - Flow Cytometry to join IQVIA Laboratories at Valencia, CA.We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary:The Senior Scientist - Flow Cytometry is responsible for developing and optimizing assays and methods of moderate complexity within the Translational Science Laboratory. This role supports timely delivery, technical troubleshooting, cross-functional collaboration, and scalable laboratory operations. What You'll Be Doing:Plan the assay and method development process and write scientific methodsExecute method development studies and support validation activities as neededTroubleshoot assays and optimize processes to improve performance and sustainabilityTransfer developed methods into the validation process and support analytical testing deliveryCollaborate across functions to ensure methods are scalable and sustainable in laboratory operationsLead low to moderately complex technical projects and guide assigned team members to meet deliverablesMentor and train junior staff while contributing to reports, presentations, and scientific communications What We Are Looking For:Bachelor's degree in a relevant scientific discipline is required4 years of related experience in method or assay development or specific methodology areaExperience with assay/method development, troubleshooting, and process optimization in a laboratory environmentSound knowledge of scientific principles, theories, concepts, and state of the art instrumentationOther equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Strong organizational skills and close attention to detailEffective communication and presentation skills with the ability to work across functionsAbility to handle multiple tasks simultaneously and independently while meeting timeline expectationsSound troubleshooting capabilities and application of root cause analysis and advanced problem solving techniquesAbility to establish and maintain effective working relationships with coworkers, managers and clients 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 $64,200.00 - $133,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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

Job OverviewSecure and retain business through professional, consultative, proactive sales activities directed at decision-makers and decision influencers at existing and new clinical sponsors. Essential Functions• Actively prospect and leverage potential new business opportunities within specified customer account(s).• Cultivate strong, long-term relationships with key decision-makers within Account and develop in-depth knowledge of the customer organization.• Maintain general knowledge of all IQVIA services for appropriate cross-sell opportunities.• Aggressively pursue awareness of competitive activities, positioning and pricing, which includes specific reasons for awards and non-awards.• Identify and respond to customer needs in order to define potential opportunities.  Propose appropriate strategy/solution to customer.• Coordinate with contracts/proposals to develop proposal.• Work with operations and functional managers to identify sales team and prepares and leads the sales presentation. Educate team participants in customer culture, operational needs/methods and sales techniques needed to close the sale.• Handle follow-up related to the sale and drive completion of contractual documents.• Adapt successful strategies and tactics to meet market demands and financial targets.• Maintain high visibility within customer organization.  Monitor customer satisfaction by communicating regularly with customer.• Establish and execute a comprehensive sales plan for each target account.  Ensure appropriate strategy/solution is proposed to customer.   Monitor actions and results against plans.• Analyze potential opportunities and develop sales plans for each target account. Ensure appropriate strategy/solution is proposed to customer.• Monitor actions and results against plans.• Record all customer sales related activities in CRM system.• Prepare sales activity report for Sales Management as required.• Serve as a liaison between the customer and technical and operational groups at IQVIA, Inc. Qualifications• Bachelor's Degree in Business Management Req• 10 years related experience, including 3 years of relevant industry (CRO/Pharmaceutical) and/or sales experience Req Or• Equivalent combination of education, training and experience Req• Proven track record at mid-level and high-level contacts• Strong organizational, planning, project management skills• A developing record of customer contacts at the outsourcing, procurement and mid - management level• Excellent Business/Industry awareness and a thorough understanding of industry trends and impact on the business• Excellent analytical skills in assessing and interpreting customer business data• Ability to maintain demanding timelines• Ability to influence others internally and externally• Adaptability and flexibility to changing priorities• Demonstrated ability to work creatively in a fast-paced environment• Exceptional attention to detail and ability to work simultaneously on multiple priorities• Ability to work independently and as a team player• Excellent skills using Microsoft Office Suite: MS PowerPoint, MS Word, and MS Excel• Excellent oral and written communication skills• Ability to establish and maintain effective working relationships with coworkers, managers and clients 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 OverviewUnder moderate supervision, executes the feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level.Prepares and manages site documentation; reviews and negotiates site documents and contracts with sites and sponsors; maintains, reviews, and reports on site performance metrics; serves as the primary point of contact for investigative sites; tracks completion of appropriate documents for sites; ensures contracts are fully executed; and establishes project timelines.  With moderate oversight and supervision, perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or internationalregulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions• With moderate oversight and supervision, serve a Single Point of Contact (SPOC) to perform site maintenance, amendment, and site support activities, with involvement in site activation activities as needed, for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the  Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.• Prepare site documents, reviewing for completeness and accuracy.• Inform team members of completion of regulatory contractual. and other documents for individual sites.• Distribute completed documents to sites and internal project team members.• Update and maintain internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.• Review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents. Requires advanced knowledge within a specific discipline typically gained through extensive work experience and/or education. • Manage ongoing study maintenance activities throughout the study lifecycle, including protocol amendments, site updates, essential document maintenance, and implementation of sponsor-driven changes. • Support site budget and contract negotiation activities, including review, preparation, tracking, and coordination with investigative sites and sponsors to facilitate timely study start-up and amendment implementation. • Coordinate and manage IRB/EC submissions and maintenance activities, including initial submissions, amendments, in accordance with local regulatory requirements and site procedures. • Partner with investigators, site personnel, sponsors, and internal stakeholders to proactively identify and resolve start-up, regulatory, and maintenance issues that may impact study timelines. • Maintain effective relationships with investigative sites and act as a key contact to support site engagement, issue escalation, and timely completion of start-up and maintenance deliverables. • Monitor start-up and maintenance performance metrics and provide timely updates, risk identification, and escalation of potential delays to project teams and management as appropriate. Qualifications • Experience in Clinical Research, including Regulatory Start-Up, CRA, Study Coordinator, or Site Management roles is preferred. • Experience with IRB submissions (initial and maintenance) and site budget/contract negotiations (initial and amendments) • Ability to communicate effectively in English, including participation in teleconferences and preparation of written communications with global teams and sponsors. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Visão geral do trabalho   Sob orientação, fornece suporte para as necessidades de marketing da Unidade de Negócios Pharma, fornecendo materiais executivos com protagonismo e inovação,  interagindo com diversos stakeholders internos e externos.   Principais responsabilidades Gerar e atualizar reports para potencializar Go-To-Market e discussões de planejamento comercial da BU. Participar de reuniões de negócio com os clientes. Desenvolver apresentações executivas das soluções (teasers) e de mercado para clientes estratégicos. Fornecer suporte no desenvolvimento de JBPs em clientes chave. Responsável pela criação e manutenção de awareness da BU, sejam conteúdos recorrentes, para eventos ou soluções. Fornecer suporte no pós venda aos clientes Blue Ocean Pharma. Participação ativa no desenvolvimento de novas soluções, interagindo tanto com clientes quanto stakeholders internos.   Qualificações Formação superior completa (Administração, Marketing, Engenharia, Sistemas ou áreas correlatas). Experiência profissional prévia com escopo semelhante ao da posição. Conhecimento nível avançado em Power Point e Excel. Capacidade de comunicação e relacionamento com vários níveis da organização (escrito e oral). Perfil organizado, criativo, planejador, com senso de urgência e capacidade de síntese. Disponibilidade para trabalhar no modelo híbrido em São Paulo/Capital (4x presencial). Inglês intermediário. Diferenciais Conhecimento da coleta de dados e soluções da IQVIA Experiência no setor farmacêutico 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 OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.• Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH 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 Degree in scientific discipline or health care preferred. Req• Equivalent combination of education, training and experience may be accepted in lieu of degree.• Some organizations require completion of CRA training program or prior monitoring experience.• Basic 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 Title: Clinical Trial Nurse - Per DiemWork Set-Up: Local Travel – In patient Home Are you a Registered Nurse interested in Clinical Trial work? IQVIA is looking for qualified Registered Nurses interested in community and clinical trial work to visit clinical trial patients in their homes. You will be responsible for going to patient homes to assist with conducting research, collecting data and samples to help evaluate safety/efficacy of a new medication. The visits/hours can be arranged to suit your current work schedule but need to be in the morning/early afternoon. Preferably we look for PRN Nurses or Nurses who already work part time. Responsibilities Complete all reports and written assignments in a timely, accurate, and thorough manner per set timelines and customer expectations. Maintain a high level of professional standards in all interactions with patients and customer contacts. Read, understand, and adhere to important documents such as fraud and abuse guidelines, FDA guidelines, Pharma code, and HIPAA guidelines and memos regarding policy and procedures. Role of Nurse During Visit: Collecting samples and required information and data. Drawing blood, taking vitals, and conducting urine tests. Administering medication if needed. Labeling and shipment of samples. Reporting of adverse events. Inputting reporting and event notes post-assignment. Tasks can vary depending on the trial. Requirements: Active RN license in home state. BLS certification required. Must be comfortable with basic software programs. Recent experience in drawing blood. Flexible with your time and available on short notice. Ability to travel regionally by car, and willing to travel up to 90 miles if needed. Possess a cellular phone, reliable transportation, and access to the internet. Ability to stand for long periods of time; bending or kneeling may be required. You will have a flexible schedule, an opportunity to travel, grow, and expand into new opportunities while earning supplemental income and gaining exposure to clinical trials. Please note, this position is not eligible for sponsorship. #LI-CES and #LI-DNP #LI-HCP IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Visão de TrabalhoEstamos buscando um representante para atuar na validação, aprimoramento e finalização do painel de médicos especialistas em Hematologia, contribuindo para um projeto estratégico de expansão e fortalecimento do ecossistema de tratamento. Principais Responsabilidades- Promover os produtos de terapia avançada CAR-T, fomentando o encaminhamento de pacientes para os centros tratadores.- Validar, aprimorar e atualizar o painel de médicos da área de Hematologia.- Realizar mapeamento de especialistas, centros de referência e oportunidades regionais.- Produzir relatórios e insights sobre engajamento, necessidades e gaps identificados em campo.- Ampliar o awareness sobre terapias avançadas dentro da especialidade.- Discutir sobre as necessidades não atendidas no tratamento de cânceres hematológicos.- Facilitar a conexão entre médicos encaminhadores e centros especializados para fortalecer o fluxo de referenciamento.- Estabelecer relacionamento com stakeholders da área e apoiar iniciativas de educação médica.- Atuar como ponto de contato regional, garantindo alinhamento com as diretrizes do projeto. Requisitos- Formação superior completa, preferencialmente na área da saúde (Enfermagem, Farmácia, Biomedicina ou áreas afins)- Experiência com projetos envolvendo especialistas médicos ou indústria farmacêutica.- Conhecimento em Oncologia e/ou Hematologia (preferencialmente Hemato).- Boa comunicação, capacidade analítica e habilidade para conduzir mapeamentos estratégicos- Disponibilidade para viagens frequentes.- CNH categoria B válida.- Veículo próprio em boas condições.  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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

Únete a nosotros en nuestro emocionante trayecto! IQVIA ™ es The Human Data Science Company ™, enfocada en el uso de datos y ciencia para ayudar a los clientes de la salud a encontrar mejores soluciones para sus pacientes. Formada a partir de la fusión de IMS Health y Quintiles, IQVIA ofrece una amplia gama de soluciones que aprovechan los avances en información, tecnología, análisis e ingenio humano para impulsar la atención médica. Actualmente nos encontramos en la búsqueda de profesionales interesados en ser parte de un gran proyecto con un importante socio de negocios.  Acerca del Rol Buscamos un Promotor para fortalecer la ejecución en punto de venta dentro del canal farmacia. Este rol será clave para asegurar la correcta visibilidad de la marca, el cumplimiento de estándares de ejecución, la capacitación del personal de farmacia y el levantamiento de información estratégica del mercado, siempre bajo los más altos estándares éticos y regulatorios. 🧩 Responsabilidades Clave 1. Ejecución en punto de venta Instalar y mantener materiales POP, displays y elementos de visibilidad aprobados por la marca. Asegurar el cumplimiento de los estándares de ejecución en farmacias clave (presencia, precios, material actualizado, entre otros). Monitorear y documentar la ejecución mediante reportes fotográficos y plataformas asignadas. 2. Capacitación y relación con dependientes Brindar capacitaciones breves al personal de farmacia sobre productos a su cargo (beneficios, categorías y manejo responsable de la información). Construir relaciones de confianza con los dependientes para fortalecer la recomendación de los productos. Detectar necesidades y oportunidades de capacitación continua. 3. Levantamiento de información Recoger precios propios y de la competencia en cada visita. Levantar información sobre disponibilidad, stock, promociones y materiales activos. Reportar insights relevantes del mercado, barreras y nuevas oportunidades detectadas. 4. Reporte y comunicación Elaborar reportes semanales y mensuales con hallazgos, fotografías y métricas clave. Alimentar plataformas de seguimiento de ejecución y precios. Comunicar incidencias o alertas a su Trade Marketing Partner asignado. 🧠 Perfil del Candidato Ideal Formación académica afín al puesto Experiencia en ejecución en punto de venta, trade marketing o canal farmacia. Conocimiento básico de materiales POP y levantamiento de información en campo. Excelentes habilidades de comunicación, negociación y relaciones interpersonales. Orientación a resultados, y acostumbrado a trabajar de forma autónoma. Permiso de conducir vigente y disponibilidad para desplazarse a nivel nacional. 🚀 ¿Qué ofrecemos? Oportunidad de formar parte de una compañía farmacéutica líder a nivel global. Desarrollo profesional dentro de un entorno ético, colaborativo y enfocado en impacto positivo en la salud. Capacitación continua y acompañamiento del equipo de Trade Marketing. #LI-CES IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Here, at IQVIA, we are building our internship program around smart, talented students that are excited about shaping the future of human health. As an IQVIA intern, you are able to create your own experience through insightful interaction with many different business units across the organization that will allow you to help us develop outside the box solutions to help solve some of the most important problems facing the healthcare industry. Every intern experience at IQVIA is unique and with our dedicated Early Talent Team here to take care of you, each intern will experience an inclusive intern community, fireside chats with executives, lunch & learns with various business units, access to our Employee Resource Groups, mentorship, skill shares, end of season presentations and much more! Join the IQVIA Intern Program today! If you have a passion for making a difference in healthcare, then consider joining the company that created the Human Data Science industry. PURPOSE: This role is ideal for current college or recent graduate students. This position will provide exposure to and provide hands-on experience working with a group of global and experienced business professionals within our organization.                                                                                                                         REQUIRED KNOWLEDGE, SKILLS & ABILITIES: Enrolled in a bachelor’s program – preferably focused in Business or similar degree focus Experience with Microsoft Office applications Quick learner and highly collaborative Ability to work within well-defined guidelines and procedures Detail-oriented with good organizational skills Proficient data entry skills/typing Able to self-direct 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 $27,600.00 - $69,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Clinical Project Managers are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Clinical Project Manager is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA’s suite of solutions to drive operational excellence and strategic leadership with our customers. Main Responsibilities• Responsible for delivery and management of smaller, less complex, regional studies.• Develop integrated study management plans with the core project team.• Accountable for the execution of clinical studies, or assigned portion of clinical studies, per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.• Set objectives of the core project team and/or sub-team(s) according to agreed upon contract, strategy and approach, effectively communicate and assess performance.• Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.• Monitor progress against contract and prepare/present project and/or sub-team information proactively to stakeholders internally and externally.• Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts.• Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and/or sub-team members and planning/implementing appropriate corrective and preventative action plans.• May serve as primary or backup project contact with customer and would then own the relationship with the project’s key customer contacts, as well as communicate/collaborate with IQVIA business development representatives, as necessary.;• Build the cross-functional project team and lead their efforts; responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.;• Ensure the financial success of the project.• Forecast and identify opportunities to accelerate activities to bring revenue forward.• Identify changes in scope and manage change control process as necessary.• Identify lessons learned and implement best practices.• May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.;• Adopt corporate initiatives and changes and serve as a change advocate when necessary.• Provide input to line managers of their project team members’ performance relative to project tasks.• Support staff development and mentor less experienced project team members on assigned projects to support their professional development. Required Skills and Qualifications• Bachelor's Degree Life sciences or related field• 5 years of prior relevant experience including extensive experience in clinical project management.• Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Experience in Regulatory and Ethics requirements in the region (East Africa). • Therapeutic area knowledge in Malaria, Sickle Cell, HIV.• Strong written and verbal communication skills including good command of English language.• Ability to work through others to deliver results to the appropriate quality and timeline metrics, monitoring/managing performance and providing feedback, experience productively partnering cross functionally and with customers to advance work effectively and efficiently.• Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.• Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.• Results-oriented approach to work towards delivery and output.• Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving.• Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint.• Ability to establish and maintain effective working relationships with coworkers, managers and clients.• Ability to work across geographies displaying high awareness and understanding of cultural differences.• Good understanding of project financials including experience managing, contractual obligations and implications. Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewUnder guidance, bridges and codes data into IQVIA systems. Essential Functions• Codes data, as required, transforming incoming paper data from suppliers to electronic data files.• Interprets written responses and enter into electronic coding systems allocating data to standard reference systems.• Performs quality assurance on coded data to ensure it accurately reflects the paper data submission.• Bridges data, comparing incoming transaction data with IQVIA’ reference data files to make a match or bridge between the two using manual or automated processes. Qualifications• High School Diploma or equivalent  Req• Three (3) years work experience in which PC literacy skills including Word, Excel have been gained. Req• Ability to carry out some analysis and information gathering to resolve problems on routine matters.• Developing knowledge of the company's products and pharmaceutical industry. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Únete a nosotros en nuestro emocionante trayecto! IQVIA ™ es The Human Data Science Company ™, enfocada en el uso de datos y ciencia para ayudar a los clientes de la salud a encontrar mejores soluciones para sus pacientes. Formada a partir de la fusión de IMS Health y Quintiles, IQVIA ofrece una amplia gama de soluciones que aprovechan los avances en información, tecnología, análisis e ingenio humano para impulsar la atención médica. Actualmente nos encontramos en la búsqueda de profesionales interesados en ser parte de un gran proyecto con un importante socio de negocios. Agente de Call Center: Industria Farmacéutica  Objetivo: Ayudar al equipo realizando llamadas a personal médico, con tal de validar y completar información en las bases de datos de IQVIA. Funciones Principales - Realización de encuestas para el sector salud, cómo médicos e instuciones (llamadas de salida) - Realización de búsquedas en Web - Envío de correos electrónicos - IMPORTANTE: NO SON VENTAS NI COBRANZAS Requisitos - Bachillerato o Preparatoria - Experiencia mínima de 6 meses como Call Center (en llamadas de salida) - Zona de trabajo: Col. Nápoles (Cercanos al WTC).- Residir en Ciudad de Mexico - Etiqueta telefónica - Manejo de Excel Ofrecemos: -Salario Base -Bono de productividad (pagado al 100% de KPI´s y con base a las políticas internas) - Vales de despensa - Seguro de vida - Seguro de Gastos médicos menores individual - 50% prima vacacional - Superiores a la Ley - 30 días de aguinaldo - Superiores a la Ley Esquema de trabajo Lunes a Viernes de 9am a 6pm. Modalidad híbrida trabajando un día en oficina, cuatro días en casa. Personas interesadas aplicar por este medio. #LI-CES#LI-DNP#LI-LATAM  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for completeness. Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow. Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training. Qualifications Bachelor's degree in Healthcare field or equivalent required. 1 of experience as a Study Coordinator or 3 years administrative support experience (INTERN role) required in the industry. Local basic Regulatory knowledge. Previous clinical research experience will be highly valued, but not mandatory. English advanced. Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint. Written and verbal communication skills. Effective time management and organizational skills. Ability to establish and maintain effective working relationships with coworkers, managers, and clients. Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry dedicated to creating intelligent connections that deliver unique innovations and actionable insights. We help to speed drug development, ensure product quality and safety, improve commercial effectiveness, get the right treatments to patients, improve access and delivery of healthcare, and ultimately drive better health outcomes. With approximately 90,000 employees, IQVIA conducts operations in more than 100 countries. Switzerland is the biggest world-wide location for pharmaceutical and healthcare corporations, with most of the global leading and emerging players having established their headquarters there.  IQVIA Switzerland is responsible to serve all Swiss-based Clients across their international footprint, delivering solutions for both Global and European operations head offices, as well as for the local market of their Swiss affiliates. By joining as a Client Service Specialist you will have the opportunity to work under the direct report of the Swiss Client Service team based in Switzerland, supporting our Swiss-based clients (pharma- and medical device companies) with customer support, CRM maintenance, billing, client communication, general administration, and sales planning activities. Role description: Support of Local Swiss Team in Sales Preparation and Customer Support Activities Creation of Price Calculations and Client Offers/Contracts Maintenance and Update of Sales Activities in our CRM system (Salesforce) Preparation of Billing Notification Forms Coordinate and align with cross-functional teams (e.g., Production team, BI team, Supplier team) to ensure seamless high-quality and consistent service deliverables Maintain regular communication with clients, acting as a key point of contact for day-to-day requests and inquiries (client relationship management) Collaborate closely with Key Account Managers to support and manage a dedicated portfolio of clients Creation and dispatch of client information material (monthly dispatch of client reports, quarterly PowerPoint presentations etc.) General administration tasks like management of Shared Mailbox and internal documentation update & maintenance Creation and Update of Power Point Presentations Confidently present and communicate insights to internal senior stakeholders as well as in client-facing settings Support Sales Team in Account Planning and Stakeholder Mapping Requirements: Commercial education or relevant Bachelors degree in a commercial or a Life Sciences discipline Good skills in Microsoft Office (esp. Excel, Word, Power Point) Reliable person with high ownership and able to work independently 2 -5 years of Experience in administration and/or data analysis Strong capability in managing priorities so that deadlines are met while retaining consistent, high quality outcomes Adaptability and ability to learn quickly and apply new knowledge Fluent written and spoken English are required, good command of German language skills Highly effective communication and remote working skills Our offer Interesting and diverse tasks in an innovative, modern, and international company Hybrid working model (home office & office workplace), and flexible working hours A steep learning curve and professional development opportunities in a dynamic team with flat hierarchies Attractive social and company benefits (restaurant ticket, medical insurance) IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Job Overview:The IT Internal Auditor position actively participates as a member of the audit team responsible for evaluating risks and controls within IQVIA’s business applications, IT infrastructure, and IT internal control environments with a focus on confidentiality, integrity, and availability of information.Successful individuals in this role will demonstrate an ability to learn and apply the IQVIA internal audit methodology across all phases of the audit lifecycle from planning to reporting. Specific activities, include developing an understanding of the technologies under review, assisting with defining the audit scope, identifying key risks and controls within the audit area, designing, executing, and concluding on testing of key controls, and assisting with development of draft audit report observations for communication to audit stakeholders.In this role you will work closely with the IT Audit Managers and Director along with other Internal Audit colleagues and external teams including the Chief Information Officer (CIO) management team and their direct reports. You will be a part of a global organization responsible for executing technology audits across IQVIA’s global and regional business units and core support functions. Lastly, you will be responsible for performing testing as part of the IQVIA Sarbanes-Oxley (SOX) compliance testing program.This position may require up to 15% travel including international travel which may include weekends.Essential Functions: Executes IT internal audit reviews and testing according to the annual IT Internal Audit plan, including fieldwork testing, documentation of results, and completion of workpapers in accordance with relevant internal and external auditing standards to determine adherence to guidelines and regulations and evaluate the effectiveness of internal controls. Supports the VP – Internal Audit, Audit Directors, and Audit Managers in delivering internal audit reviews. Assists in all audit processes, including risk assessment, planning, audit program development, execution of audit procedures, and communication of audit results and best practices to leadership Determines compliance with IT policies and procedures Performs analytical testing and review Identifies internal control weaknesses and makes improvement recommendations Performs Sarbanes-Oxley IT compliance work Execute IC calculations at end of quarter Develops and maintain effective working relationships with Internal Audit stakeholders Assists in preparation of draft audit reports for management review Participates in the continuous improvement of the Internal Audit department, including providing training and feedback related to audit activities. Minimum Education, Experience, & Specialized Knowledge Required: Bachelor’s Degree in Information Technology, Cybersecurity, Information Systems, Computer Science, Business Administration, or related area Excellent written and oral communication skills, strong organizational and analytical skills, and project management experience Minimum of 2 years of professional experience, preferably including internal audit. Auditing work experience is preferred; however, business/operations experience may be deemed adequate Knowledge of the Sarbanes-Oxley Act and methodologies for achieving compliance Understanding of general auditing (GAAS) principals Strong interpersonal skills with ability to work closely with people at all levels of the organization Demonstrated ability and desire to improve individual performance and advance the efficiency and effectiveness of the department Ability to work in a highly complex environment under general direction Ability to effectively communicate audit issues and recommendations in both technical and non-technical terms to management. Working knowledge of general and application controls, systems/application development, business continuity and disaster recovery, and technology areas including networks, communications, operating systems, databases, cloud computing, web technologies, and information technology governance standards and industry best practices (e.g., ISO, NIST, ITIL, etc.) Preferred Qualifications: Has obtained or actively pursuing professional technology certification such as Certified Information System Auditor (CISA), Certified Internal Auditor (CIA), Certified Information Security Manager (CISM), Security+ or equivalent. Experience using data analytics and visualization tools such as Power BI, Spotfire, Alteryx, etc. Familiar with data privacy regulations and controls (e.g., HIPAA, CCPA, GDPR, etc.) Familiar with LEAN principles and practices Familiar with Microsoft Azure or Amazon Web Services (AWS) concepts and services Excellent written and oral communication skills, strong organizational and analytical skills, and project management experience IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Join us on our exciting journey!We are recruiting a bold mind to work as a Senior Client Service Analyst with experience in client-facing roles, customer success, account management, or healthcare/pharmaceutical analytics. In this role, you will partner with leading pharmaceutical clients, helping them maximize the value of IQVIA's market intelligence solutions while building strong, long-term relationships. You will combine analytical thinking, problem-solving, and stakeholder management to support client success and business growth. Essential Functions: Ensures fulfillment of contract specifications and ad-hoc client requests to build client satisfaction, under supervision.Assists team members to build, establish and maintain effective business relationships with clients to proactively support their needs as their day-to-day contact, possibly focused on a specific product or service.Ensures, through review and verification, that the product deliverable meets the customer's specifications, including timeliness and quality.Partners with the account manager and clients to derive optimum value from IQVIA products and services by explaining and expanding the usage of current IQVIA deliverables and identifying revenue opportunities within existing clients.Maintains effective internal communications with sales and client service support to keep all apprised on activities with the client.Monitors performance against existing service agreements and ensures client’s obligations are met.Researches, analyzes and responds to client that require an in-depth understanding of the client, specific business line, and/or therapeutic market.May conduct product/services and process training for clients and other employees.May conduct service meetings at client sites.Represents IQVIA on external client projects.May mentor and lead other client service reps and represent the manager in their absence.Qualifications: Bachelor's degree or equivalent experience. Healthcare or L&S would be a plus.Experience in Client Services, Customer Success, Account Management, or a similar client-facing role.Strong analytical mindset and confidence working with data.Excellent communication and stakeholder management skills.Ability to build trusted client relationships and manage challenging situations.Experience within healthcare, pharmaceuticals, life sciences, or market intelligence is a plus.Proficiency in Excel and other business tools.We invite you to join IQVIA™ IQVIA™ is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com IQVIA™ is an equal opportunity employer. We make employment decisions based on qualifications and merit. We prohibit discrimination based on any unlawful consideration such as age, race, national origin, gender or other "protected status“. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Overview Provide programming expertise to develop and maintain programs to meet internal and external clients’ needs. Provide and assist in leading the development of project-related solutions to a wide range of statistical programming tasks. Essential Functions • Perform and plan: (i) the programming, testing, and documentation of programs for use in creating statistical tables and listing summaries, (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients and (iii) the programming of database quality control checks.• May program the integration of databases from multiple studies or sources, under supervision.• Develop programming documentation including specifications, as appropriate, under supervision.• Provide advanced technical expertise in conjunction with internal and external clients, and bring project solutions to teams and department, under supervision.• Develop, implement and validate new process technologies, macros and applications under supervision.• Fulfill project responsibilities at the level of assisting the statistical team lead.• Understand the Scope of Work, estimate the work completed, and manage Out of Scope single studies, under supervision. May manage budget and resource requirements and provide revenue and resource forecasts for single studies. May be required to understand budget and quote assumptions. Qualifications• Master's Degree Computer science or related field Or• Bachelor's Degree biostatistics or related field and 1 year relevant experience• Equivalent combination of education, training and experience • Knowledge of programming, statistics and/or clinical drug development process• Experience with patient-level, longitudinal data.• Strong programming skills in R or SAS (or both). • Organizational, interpersonal and communication skills• Ability to effectively handle multiple tasks and projects• Excellent accuracy and attention to detail• Aptitude for mathematical calculations• 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. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Job OverviewProvide experienced technical expertise to develop process methodology for department to meet internal and external clients’ needs. Plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements. Essential Functions• Perform, plan and co-ordinate the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing summaries and (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and plan the programming of database quality control checks.• Program and plan the integration of databases from multiple studies or sources.• Develop and co-ordinate programming documentation including plans and specifications, as appropriate, for complex studies.• Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and department, for complex studies.• Perform, plan and co-ordinate the development, implementation and validation of new process technologies, macros and applications.• Fulfill project responsibilities at the level of statstical team lead for single complex studies or group of studies.• Understand the Scope of Work, budget and quote assumptions, estimate the work completed, manage Out of Scope and resource forecasts for single studies. May manage project budget and resource requirements, and provide revenue forecasts for single studies.• Provide training and guidance to lower level staff. Qualifications• Master's Degree Computer science or related field and 8 years relevant experience Req Or• Bachelor's Degree Computer science or related field and 8 years relevant experience Req• Equivalent combination of education, training and experience in lieu of degree Req• Knowledge of statistics, programming and/or clinical drug development process• Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro Language• Good organizational, interpersonal, leadership and communication skills• Ability to effectively manage multiple tasks and projects• Excellent accuracy and attention to detail• Ability to establish and maintain effective working relationships with coworkers, managers and clients IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

We are seeking a detail-oriented Software QA Engineer to join our team. In this role, you will play a key part in ensuring the quality, reliability, and performance of technology solutions. You will work closely with cross-functional teams, participate in both manual and automated testing, and contribute to continuous improvement of quality assurance processes.Key ResponsibilitiesAnalyze business and data requirements to ensure test coverage and accuracyPerform both manual and automated testing of applications and systemsCreate, review, and maintain test data for various testing scenariosIdentify, log, and track defects while providing regular updates on test progressDocument test cases, test processes, and quality outcomes clearly and accuratelySupport the preparation of quality metrics and status reports for stakeholdersApply QA best practices and contribute to ongoing process improvement initiativesCollaborate with cross-functional teams to enhance testing strategies and workflowsRequired QualificationsBachelor’s degree in Computer Science, Information Technology, or a related field (or equivalent experience)1+ year of experience in software quality assuranceBasic knowledge of at least one database management system (DBMS)Strong analytical thinking with excellent attention to detailGood communication and teamwork skills for effective collaborationEagerness to learn, adapt, and grow in a fast-paced environmentNice to HaveExposure to healthcare or similar regulated domainsUnderstanding of compliance standards (e.g., data privacy, regulatory frameworks)Familiarity with domain-specific workflows or transaction processing systemsIQVIA 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 Senior Supply Chain Coordinator to join IQVIA Laboratories at Indianapolis, IN.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:Ensure all shipments to and from sites, both locally and internationally, comply with applicable regulations, courier specifications, and study requirements. Resolve shipping challenges and support logistics operations while maintaining high standards of accuracy and efficiency. What You'll Be Doing:Coordinate logistics, kit production, and inventory control activities to support laboratory operationsEnsure compliance with global shipping regulations, including customs, FDA, and dangerous goods requirementsPrepare shipping documentation such as commercial invoices, letters of instruction, and airway billsLiaise with project management teams to determine shipping needs and provide logistics guidanceTrack, trace, and resolve shipment issues to ensure timely deliveryMaintain courier systems, address databases, and ensure accurate data within QLIMSMonitor inventory levels and maintain adequate stock of shipping materialsSupport training of staff and contribute to process improvements for logistics efficiency What We Are Looking For:High school diploma or equivalent2 year of related experience.Knowledge of import/export regulations and global shipping processesExperience using courier systems and logistics tracking tools (e.g., QLIMS or similar systems)Other 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 problem-solving skillsDetail-oriented with the ability to manage multiple priorities in a fast-paced environmentAbility to build and maintain effective working relationships with internal and external stakeholders What We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.To learn more about our benefits, visit https://jobs.iqvia.com/benefits.If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $46,000.00 - $95,900.00. 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 welfare and/or other benefits.

Grade : 130 or 140 Location : Gurugram/Bengaluru Role Purpose:•Responsible for generation of forecast inputs and assumptions required for a syndicated drug-level forecast database product in Global Market Insights, reporting into Manager, Data Analytics.Principle Accountabilities•Build and analyze the rationales for country specific forecast assumptions for multiple indications using secondary sources and his/her understanding of therapy area, and country/geography specific nuances.•Under broad guidance from manager, performs accurate and timely provision of manual inputs and assumptions to augment the automated generation of syndicated drug-level forecasts.•Must be aware of MIDAS data caveats and should be able to identify inconsistencies/gaps and rectify them by using secondary data sources.•Must be able to understand and manipulate quantitative data, particularly in generating test sets for comparison to automated data outputs.•Follow best practice in ensuring quality and timeliness of input data capture and assumptions such as projected drug launch dates, loss-of-protection dates and share-shift assumptions.•Support manager in driving a consistent approach to the application of inputs and assumptions across drug classes, countries and diseases. This consistent approach is essential in the creation of standardized outputs that can be held in a data cube that can be segmented by key industry dimensions including drug, therapy, company, country and disease.Minimum Education, Experience, & Specialized Knowledge Required•Bachelor’s/Masters Degree with previous professional experience preferably working with pharmaceutical data.•5 or more years work experience in a similar environment would be considered.•Understanding of pharmaceutical domain and broad level understanding of major economies pharmaceutical environment will be advantageous.•Must be diligent with secondary research using search engines and clinical trial websites.•Prior experience of pharmaceutical forecasting, model development, and advanced excel.Additional Requirement:•Must be comfortable with high-throughput data transformation.• Experience in a service or business to business environment• Ability to work within cross-functional teams• Ability to learn new concepts quickly• Ability to deliver against challenging deadlines• Strong attention to detail• Ability to work in complex, matrix organization• Ability to work multiple projects at one time. • Excellent 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.

Location : Gurugram , Bengaluru The Country Manager will be responsible for the research, writing/report production and forecasting for 3-4 Market Prognosis countries. Thecountry manager will also manage junior analysts in the team as well as contribute to other MP deliverables like Market Prognosis Global,Regional Overviews.Expectations:1. Deliver high quality forecasts and reports for assigned countries on scheduled timelines.2. Ensure work is delivered within budget. Support internalization process, ensuring internal report writing is successfully adopted.3. Be able to defend and justify analysis and forecasts presented, based on research conducted and expertise established, particularly,forecasts, key issues, change in prognosis, events.4. Collaborate closely with onshore and GOC colleagues to ensure consistent and latest models are employed.5. Build effective relationships with local offices to support primary market research and validation of forecasts and reports.6. Create documentation (SOPs, Checklists) for projects7. Consistently deliver high quality output.8. Support further development in achieving synergies between the various forecasting services.Education:1. Graduation in Life Sciences/Pharma related subject + Master’s Degree or MBA.2. For candidates with 6+ years of experience, a Post Graduate Degree or Diploma is not essential.Experience:1. 4 to 8 years of experience in pharmaceuticals analytics/with a minimum of 2-3 years of forecasting experience.2. Demonstrated experience of independently handling projects, handling client engagements, working on short- and long-term deadlines,and robust project management3. Working knowledge of VBA, ForecastPro will be an added advantageSkills:1. Proficient in MS Office – Excel, Word, PowerPoint2. Excellent communication (verbal/written) and interpersonal skills and excellent reading comprehension skills3. Project management with the ability to perform under pressure4. Should possess working knowledge of the pharma industry5. Good secondary research 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.