IQVIA

Health Information Technology Specialist Player Coach Do you have a passion for harnessing technology to make a positive impact on patients’ lives? Do you have Electronic Healthcare Record (EHR) as well as coaching, mentoring, and leadership experience and are looking for a rewarding career path within the Health Information Technology field? We are excited to announce that we are looking for a Health Information Technology Specialist Player Coach to support an IQVIA pharmaceutical client partnership. This role blends direct field execution with team leadership and is responsible for driving operational excellence, coaching field team members, and serving as a key liaison between the client, the field team, and IQVIA leadership. This individual will have the unique opportunity to be a part of multiple cardiovascular brands in the US market as a Health Information Technology Specialist Player Coach. The primary focus of this role will be to support integration of the brand into EHR systems across priority accounts, helping identify and address barriers that affect patient care, access, treatment processes, patient identification, and overall end-user experience In addition, the Health IT Specialist Player Coach will be responsible for sharing Electronic Health Record insights to enhance patient care and support population health approaches across both in-patient and outpatient sites of care at priority accounts. Other responsibilities include developing and implementing comprehensive customer specific plans, as well as working in a collaborative manner with Account Management, Medical and Cross functional account teams The Health IT Specialist Player Coach will also support healthcare stakeholders including end users, clinicians, informatics, Quality, Population Health and IT teams The Player Coach also serves as the primary contact for the field team and provides day-to-day oversight across operations, team performance, and personnel matters. Working closely with the Health IT Director, this individual helps align strategy, support execution, and provide coaching and development to Health Information Technology Specialists. Success in this position requires a self-starter that thrives in ambiguity and can be both a strategic partner and outcomes driven.  Core Duties/Responsibilities: Health IT Specialist Identify potential gaps/barriers within EHR systems at priority IDN’s & Health SystemsProblem solve and provide solutions and resolution of EHR gapsIdentify workflow barriers and recommend scalable solutionsWorks collaboratively with customers including end users, licensed clinicians, IT informatics team, quality EHR Manager and analyst to provide meaningful insights to enhance patient careAlign resources to develop comprehensive plans by priority institutionComplete workflow assessments with institutional customers to identify potential gaps in care across the patient journeyDevelop and implement comprehensive customer specific plansWill act as matrix team Health IT Specialist subject matter expert to both internal and external stakeholders with matrix partners across account management, medical, and other cross functional partners.Share insights around optimizing EHR systems to address gaps in patient care including Inpatient, Outpatient, and Emergency Department Core Duties/Responsibilities: Coach Perform the core duties and responsibilities of the Health IT Specialist role while serving as a leader and coach to the field team, with an expected split of approximately 70% field responsibilities and 30% leadership responsibilities.Serve as the primary point of contact for the CV Health IT field team and act as the key liaison between the team and the Health IT Director for operational and personnel-related matters.Provide ongoing coaching, mentoring, and performance support to Health IT Specialists to strengthen execution, professional growth, and alignment to business objectives.Partner with the Health IT Director on recruiting, interviewing, and selecting new team members, as well as supporting onboarding and readiness of new hires.Support completion of performance reviews and employee relations matters, including performance improvement and disciplinary processes, in partnership with leadership and Human Resources.Monitor field activity, work schedules, time reporting, credentialing, and expense compliance to ensure timely completion and adherence to company policies.Conduct field visits, both in person and remotely, to observe execution, provide coaching, and identify opportunities for improved performance and consistency.Share field insights and recommendations with leadership to support program effectiveness, continuous improvement, and evolution of the Health IT strategy.Support the planning and delivery of team meetings, training programs, and educational initiatives for internal matrix partners and customer stakeholders.Build and maintain strong collaborative relationships with internal partners, including Account Executives and Sales Leadership, as well as external customer stakeholders.Maintain current knowledge of the Health IT functionality, including industry trends, EHR developments, customer needs, and competitive dynamics.Ensure all work is performed in accordance with regulatory requirements, compliance standards, and IQVIA policies and procedures.Complete administrative and reporting requirements accurately and on time, including documentation of Health IT activities and project updates as requested.Travel up to 40–60% as required.Requirements Bachelor's degree from an accredited college/university required;Minimum of 4 years working in design, build, and/or testing expertise and experience with EHR software, including: Epic, Cerner, Meditech, McKesson preferred; and/or within a Health System informatics group or team at leadership level, or similar role within a pharmaceutical company.In depth knowledge of healthcare and health information technology, and software build, and/or optimization techniquesAbility to discover issues, prioritize and problem solve to resolution Team player with the willingness/ability to work in a matrix environmentExcellent presentation skillsStrong oral and written communication skillsEnthusiastic, positive attitude, flexibilityAbility to consistently travel overnight Preferred Master’s degreeClinical IT experience, Pharmacy IT, or Nursing InformaticsPharmaceutical or Life Science Health IT Specialist experienceB2B or software sales experience#LI-CES IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is $135,000 - $145,000 annually. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA/MedTech takes the approach to helping customers drive healthcare forward in this challenging, fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities. We invite you to apply! You will be asked to create and account, which takes less than one minute and requires only a username and password. The entire application takes 5-7 minutes to complete. We are hiring an Inside Sales Representative for a reputable Medical Device Company **THIS IS A 6 MOS PROJECT WITH POTENTIAL TO EXTEND** Requirements: AA/BS/BA or equivalent practical experience; preferred2+ years inside sales, direct sales, customer service or telemarketing experience; preferredIdeal candidate will have prior service contract selling experience; have strong customer service experience; be confident, professional and a self-starterMust have excellent time management experience and ability to cultivate positive client relationships with customerHave a proven and documented sales record of successExcellent verbal and written communication skillsAbility to prospect, build a pipeline and move ongoing opportunities through the sales cycle as well as propose and discuss viable solutions with key decision makersResponsibilities: Introduce Client’s menu of service contracts to current customer baseEstablish new business sales through email and outbound phone campaignFocus on biomed and materials management departments with initial introductionIdentify the key decision makers and influencers for service contracts and review service menu options in detail, leading to the saleReview current equipment and corresponding warranty terms to provide appropriate service contract solutionsForward Client’s formal Service Menu Document to customerConduct follow-up calls and emails for feedback on service contract options initially presentedUnderstand customer needs and requirements through key listening for feedback on service menu options and provide appropriate solutions to extend, adopt new services, or upgrade for multiple yearsCraft solution with appropriate service that meets business goals based on client discussionsIQVIA MedTech CFS takes the approach to helping customers drive healthcare forward in this challenging and fast-paced environment. We help customers accelerate results, improve patient outcomes, and unleash new opportunities.  Benefits: This position is not eligible for our Medical Benefits. Vaccine/Immunization/Hospital Credentialing Requirement: A required function of this job requires individuals to enter various healthcare facilities.  Thus, upon selection, individuals must complete healthcare facility credentialing process.  To obtain credentials, individuals must meet the immunization requirements specified by the facility.  Individuals are typically required to have completed/up to date: Measles, Mumps & Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria & Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series (heavily enforced by most facilities, some require booster(s)). Please note, IQVIA complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons, however, our client’s requirements may supersede this.  #LI-CES #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is 35 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job Overview As a Regulatory Reporting Specialist, you will be involved in submitting safety reports to regulatory authorities. Review, assess, and process safety data and information received from various sources. Distribute reports/data to internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines under the guidance and support of senior operation team members. Essential Functions Process safety data according to applicable regulations, guidelines, SOPs, and project requirements. Ensure compliance with quality, productivity, and delivery standards per project requirements. Track cases as applicable to the project plan. Identify and report quality problems to senior team members. Liaise with different functional team members and health care professionals to address project-related issues. Attend project team meetings and provide feedback to the operations manager on challenges, issues, or successes. Qualifications Bachelor's degree in life sciencesLanguages: Advanced level of English; Advanced level of Portuguese.2-3 years of experience in pharmacovigilance activities (mandatory) Specifically in regulatory reporting, will be highly valued.Good knowledge of medical terminology and applicable safety databases.Strong organizational skills, attention to detail, and ability to work independently and as part of a team.Work modality: 100% home-based 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! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human ingenuity to drive healthcare forward. Job Title - Administrative Support Specialist We are looking for a highly organised and reliable Administration Assistant  to provide high‑level administrative and operational support to management. This role plays a key part in ensuring structure, efficiency, and smooth day‑to‑day operations, while supporting managers primarily based in the United States, with senior managers based in the UK. This is a fully home‑based position suitable for someone who enjoys working independently, bringing order to complex situations, and supporting multiple stakeholders in a professional, structured manner. The ideal candidate is detail‑oriented, proactive, comfortable working with data and systems, and able to maintain clarity and organization in a fast‑moving environment. Key Responsibilities Administrative Support Provide comprehensive administrative support to management, including calendar coordination, meeting organization, and follow‑up actions Prepare, format, maintain, and distribute documents, reports, presentations, and routine correspondence Organise, record, sort, and maintain files and information in line with internal standards Manage email and information flow, respond to inquiries, and route requests appropriately Coordinate travel arrangements, meetings, and appointments as required Operate standard office systems and tools to support daily administrative activities Operational & Cross‑Functional Support Support managers with administrative tasks across finance, planning, HR, IT, and other corporate services as needed Assist with data tracking, reports, and preparation of materials for leadership discussions Act as a coordination point between managers and internal teams, supporting clear communication and execution Proactively track action items, deadlines, and deliverables to ensure follow‑through Organisation & Process Support Bring structure to complex workflows by organizing information, priorities, and timelines Support process consistency and identify opportunities to improve administrative efficiency Work confidently with systems, data, and reports to ensure accuracy and transparency Handle sensitive and confidential information with a high level of discretion and professionalism Working Hours & Location Full‑time, fully home‑based role - flexible working by arrangement Role supports US‑based managers, but does not require working US time zones Qualifications - Our ideal candidate will have: Required High School Diploma or equivalent Minimum of 3 years of experience in an administrative, secretarial, or similar support role Strong organizational, prioritization, and time‑management skills Proficiency in Microsoft Office tools (Outlook, Word, Excel, PowerPoint) Strong written and verbal communication skills in English Ability to work independently in a remote setup Preferred Experience supporting senior managers or leadership teams Experience working in an international or matrix environment Comfort working with data, reports, and structured processes THIS ROLE IS NOT OPEN TO VISA SPONSORSHIP! We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™.   IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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 & 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. Are you up for a challenge? Ready to support health care companies and create valuable business insights by combining real world data with technology to provide data solutions? The role-holder will need to be a committed individual, who combines high emotional intelligence and excellent communication skills. They will thrive in a fast-paced environment, be comfortable managing conflicting priorities and have the gravitas to influence a team of senior stakeholders. They will also be a champion for thoughtful staffing, gain a detailed understanding of our team members to drive a balance between the career development of our client-facing staff and the needs of the business. The environment is dynamic and ever-changing, moving at the pace of our clients’ needs and the RM will be expected to understand the sense of urgency that is synonymous with the business. The pressure is high to resolve resourcing demands quickly, find creative solutions and make autonomous decisions.   Principal Accountabilities We are looking for an individual who can: Manage the allocation of client facing staff to client projects, business development opportunities and internal initiatives; drawing on robust negotiation skills to resolve conflicts and escalating issues when necessary Developing strong relationships across the wider resource management community; sharing resources across practices where appropriate to optimize overall productivity and realization while supporting their individual development objectives. Engage with our local and global senior leadership team to understand, plan for and ultimately meet the resourcing demands of the pipeline, ensuring that profitability is kept at the forefront of resourcing decisions. Influencing on resource selection and strategic solutions to achieve realization of utilization and effective skills / grade mix on projects. Develop a deep understanding of the development goals of the delivery team through the creation of strong relationships. Leverage that knowledge to make effective resource management decisions Monitor and communicate current and near-term delivery capacity Maintain resource management data integrity in the systems that support resource and project management decisions Flag resourcing capability gaps as an input to hiring and to provide guidance into Learning & Development Demonstrating strong commercial awareness monitor and drive compliance to our financial management system, identify and propose solutions to resolve longer term patterns relating to forecast and actual utilization, monitoring and investigating discrepancies between the data and providing insight Support HR with Performance Management biannual process On-board all new joiners to introduce Resource Management processes and understand their skills and experience Appropriately escalate conflicts and unresolvable issues to leadership team for their support Education, Skills, Experience & Specialized Knowledge Bachelor's degree, ideally in Life Sciences. 2+ years’ experience in a role related with clinical trials. Previous staffing / resource management (or related) roles, ideally in a professional services environment. But not mandatory. Strong written and spoken English language skills (this is mandatory, you'll be working in a global team). Proven problem-solving skills with strong attention to detail. Ability to build strong business relationships and influence with key stakeholders at all levels within the business. A self-starting mind-set with excellent team-based interpersonal skills with the ability to work independently with the full spectrum of our people. Good negotiation skills. Ability to rapidly assimilate multiple types of information from a variety of sources for effective decision making. Proficient in Microsoft Office applications. 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.

En IQVIA creemos que la diversidad impulsa mejores decisiones, mayor innovación y mejores resultados. Buscamos una persona organizada, orientada al detalle y con interés en el manejo de información para apoyar procesos administrativos y de análisis de datos en diferentes áreas de la compañía. Esta posición combina actividades de soporte administrativo con tareas relacionadas con la gestión, validación y análisis de información. Responsabilidades principalesGestionar y dar seguimiento a correos electrónicos y comunicaciones internas.Coordinar agendas y programación de reuniones.Elaborar y consolidar reportes administrativos y de gastos.Actualizar información en sistemas y bases de datos.Realizar validación, consolidación y revisión de datos en Excel.Generar reportes e indicadores operativos.Garantizar la calidad y consistencia de la información procesada.Apoyar actividades de seguimiento y análisis para diferentes áreas del negocio.Organizar y administrar documentación física y digital.RequisitosBachiller, técnico, tecnólogo o estudiante de carreras administrativas, contables, financieras o afines.Manejo de Microsoft Office, especialmente Excel.Atención al detalle y orientación a la calidad.Capacidad de organización y seguimiento de tareas.Habilidades de comunicación escrita.Capacidad para trabajar con información numérica y administrativa.Valoramos especialmenteExperiencia previa en procesos administrativos, back office o análisis de información.Experiencia en manejo de bases de datos, reportes o validación de información.Conocimiento intermedio de Excel (tablas dinámicas, filtros, fórmulas básicas).Capacidad para priorizar actividades y gestionar múltiples tareas.Lo que encontrarás en IQVIAUn entorno inclusivo y diverso.Oportunidades de aprendizaje y desarrollo.Participación en proyectos que impactan el sector salud.Trabajo en equipos colaborativos y orientados a la innovación.Convocatoria InclusivaEn IQVIA promovemos la igualdad de oportunidades y alentamos la postulación de personas con discapacidad interesadas en desarrollarse en funciones administrativas, operativas y de manejo de información. Como parte de esta convocatoria inclusiva y en cumplimiento de la normatividad vigente, los candidatos podrán indicar voluntariamente si cuentan con certificado de discapacidad y adjuntarlo durante su postulación. La información será tratada de acuerdo con las políticas de protección de datos de IQVIA y utilizada exclusivamente para fines de selección y cumplimiento legal. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human ingenuity to drive healthcare forward. Essential Functions: Ensures fulfilment 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, and proactively supports their needs as their day-to-day contact, possibly focused on a specific product or service.Ensures that the product deliverable meets the customer's specifications, including timeliness and quality through review and verification.Maintains effective internal communications with sales and other key account owners to keep all apprised of activities with the client. Deliver targeted reports as required.Monitors performance against existing service agreements and ensures client’s obligations are met.Carries out client research to ensure an in-depth understanding of the client, specific business line, and/or therapeutic market.Conducts product/services and process training for clients and other employees.Potentially conduct service meetings at client sites.Represents IQVIA on external client projects.Identifies and escalates potential risks or issues to the appropriate internal teams to ensure timely resolution.Provide feedback to product development teams based on client interactions to help improve future product offerings.Qualifications: Bachelor's Degree Req.Two (2) years of related work experience Req.Meeting facilitation, presentation, and training experience ReqProficiency in PC applications, such as Excel, PPT, and WordDemonstrated problem-solving, analytical, and strong customer service skillsDemonstrated ability to develop and maintain relationships in a diverse business environmentAbility to travel to clients and IQVIA offices as appropriateStrong organizational skills and attention to detail.*CVs must be submitted in English* This role is not open to visa sponsorship. A degree of flexibility re working hours is required for this role. We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. 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.

Projektleiter (m/w/d) – Healthcare IT-Systemlösungen Anstellung: VollzeitBereich: Softwaremodernisierung, Wartung & Weiterentwicklung medizinischer Abrechnungssysteme Über die RolleAls Projektleiter (m/w/d) übernehmen Sie die Verantwortung für die Planung, Steuerung und erfolgreiche Umsetzung von ITP- Projekten im Umfeld von medizinischen Abrechnungssystemen. Sie arbeiten an zentralen Modernisierungs- und Transformationsprogrammen – einschließlich Cloud-Migration, Prozessoptimierung, Qualitätssicherung und der Einführung moderner DevOps-Methoden. Ihre Aufgaben-    Projektmanagement-    Validierung und Strukturierung von Projektzielen, Anforderungen, Zeitplänen und Budgets-    Steuerung aller Projektphasen (Konzeption, Implementierung, Test, Rollout).-    Einhaltung relevanter Standards.-    Risiko- und Qualitätsmanagement.-    Verantwortung für erfolgreichen Projektabschluss.      Stakeholder- und Kommunikationsmanagement-    Aufbau und Pflege von Stakeholder-Beziehungen im Gesundheitswesen.-    Moderation von Workshops und Regelterminen.-    Erstellung von Entscheidungsunterlagen und Statusberichten.     Change- und Transformationsmanagement-    Analyse von Veränderungen und deren Auswirkungen.-    Unterstützung bei der Einführung neuer Prozesse und Technologien.-    Mitwirkung bei Schulungskonzepten.     Evaluierung & Optimierung-    Bewertung des Projektfortschritts anhand definierter KPIs.-    Identifikation und Umsetzung von Verbesserungen.-    Regelmäßige Berichterstattung. Ihr Profil-    Studium der Informatik, Wirtschaftsinformatik oder vergleichbar.-    Mindestens 5 Jahre Erfahrung im IT-Projektmanagement.-    Erfahrung im Gesundheitswesen von Vorteil.-    Kenntnisse moderner Projektmethoden.-    Ausgeprägte Kommunikationsfähigkeiten und strukturierte Arbeitsweise. Warum diese Rolle spannend ist?Sie arbeiten in einem zentralen Bereich der Digitalisierung medizinischer Abrechnungsprozesse und gestalten aktiv die Modernisierung einer komplexen IT-Landschaft. 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.

Plan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff, management, and customers. Provide consultation in interpretation ofregulations, guidelines, policies, and procedures. Support management in promotion and assessment of compliance to regulations, guidelines and corporate policies. Essential Functions• Plan, schedule, conduct, report and close audit activities in any of the countries involved with IQVIA contracts to assess compliance with applicable regulations/guidelines, customer requirements, IQVIA SOPs and project specific guidelines/instructions• Evaluate audit findings and prepare and distribute reports to operations staff, management, and customers• Provide interpretation and consultation to project teams on regulations, guidelines, compliance status, and policies and procedures• Provide consultation to customers and monitors in interpretation of audit observations and formulation of corrective action plans• Review, approve investigations, Root Cause Analysis (RCA), Corrective Action Prevention (CAPA) and Effectiveness Check (EC) plans and track till closure for quality events arising from Audits; and from Quality Issues, Inspections or during similar QA activities as assigned.• Evaluate policies and procedures for compliance with applicable regulations/guidelines and provide recommendations to management for continuous process improvements• Maintains the electronic quality management system (eQMS) and provides support in relation to the audit lifecycle• Lead/collaborate/support in QA initiatives/projects for quality, process improvements• Assist in training of new Quality Assurance staff• May be required to manage Quality Issues• May present educational programs and provide guidance to operational staff on compliance procedures• May perform pre-inspection visits at sites, host audits/inspections; ensure proper conduct of customer-initiated audits and mock regulatory inspections, and assist in regulatory facility inspections, as assigned. Qualifications• The right candidate must be Certified to conduct audits in Italy in accordance with the Italian Decree of the Ministry of Health dated 15 Nov 2011. • Travel 30-50% mainly in Europe.• 5 years experience in pharmaceutical, technical, or related area, of which 3 years in Quality Assurance Audits.• Experienced in the conduct of clinical trial Investigator site audits.• Experience in the conduct of clinical study report/data management clinical trial audits is preferred.• Knowledge of word-processing, spreadsheet, and database applications.• Extensive knowledge of pharmaceutical research and development processes and regulatory environments.• Knowledge of quality assurance processes and procedures.• Strong interpersonal skills.• Excellent problem solving, risk analysis and negotiation skills.• Strong training capabilities.• Effective organization, communication, and team orientation skills.• Ability to initiate assigned tasks and to work independently.• Ability to manage multiple projects.• 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 OverviewIndependently manage end-to-end delivery of data management services for single/multi-service projects, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products that meet customer needs. Provide leadership and vision to the team in the areas of project planning, execution, and close-out; financial management; communications; and milestone deliverables. May perform role of Data Team Lead (DTL), Program Lead, Customer Site Manager, and/or a leadership role in a specific CDM task (e.g. Subject Matter Expert (SME). Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where available, CDM guidance documents.Should have experience in study setup (all DM activities ). Did setup of minimum 2-3 studies on Rave Platform.Experience in writing URS for Data review reports.Screens and Edit Checks UAT experience.Essential Functions• Client Management: Serve as primary point of contact for customer on data management deliverables• manage multiple large studies or program of studies (possibly global) Provide leadership and senior support to DTLs on multiple large global studies/programme of global studies Provide leadership and senior support to DTLs on multiple large global studies/programme of global studies.• Provide project management expertise working with customer data managers, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections, and provide technical expertise• Lead direct negotiations with customer, e.g., timelines, financial, process, resources.• Maintain strong customer relationships• Ensure open communications with customer and IQVIA management to independently manage and meet contractual obligations• Service Management:• Meet with Data Operations Coordinator (DOC) and/or Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables• provide training and development on data management expertise to junior team members• Establish strong communications with Data Operations team, functional leads, project managers and all other stake holders• Independently manage DM service delivery with comprehensive DM process and technical expertise in executing projects• Serve as the escalation point for unresolved data issues• independently work with client data managers, vendors, internal team members for resolution• Ensure appropriate resources are assigned to meet project deliverables• Create and/or review and sign-off on all data management plan (DMP) documents• Ensure service and quality meet agreed upon specifications per the DMP and contract/SOW• Implement proactive quality management plans across multiple projects/programmes/customer account. Manage service performance and provide leadership to identify root causes of issues and implement remedial actions• Continuously look for opportunities to improve service• develop and work with team to implement plan to re-organise and drive change (possibly across a customer account)• Ensure timely follow-up and resolution of compliance issues• Serve as Subject Matter Expert (SME)• Provide leadership and expertise in a specific CDM task or technology• Serve as customer site lead for one or more customers• Train and mentor junior DTL staff in DM expertise• may coordinate the work of more junior DTL staff• Independently maintain internal tracking databases and systems• Financial Management/Business Development Support:• Independently manage SOW/budget• Review financial reports on a monthly basis and participate in project reviews as requested• Identify out of scope tasks and track change orders to completion• Participate in pricing discussions across customer account• Serve as Project Manager for single service DM projects, including financial tracking, revenue recognition, and invoicing• Independently support RFP process (review RFP documents, pricing, attend bid defense)• Other:• Independently bring process improvements and solutions to the CDM team/CDM department• Lead a focus team or global or local best practice team• Communicate lessons learned and/or present in CDM workshop(s)• Manage the development and implementation of new technology or tool• Present at professional conferences and/or publish articles in professional journals• Provide review and expert opinion in developing, revising, and maintaining core operating procedures and work instructions• Perform other duties as directed by the functional manager Qualifications• Bachelor's Degree Health, clinical, biological or mathematical sciences, or related field Req• 7 years direct Data Management experience, including 5 or more years as a CDM project lead. Equivalent combination of education, training and experience.• Previous experience and proven competence in managing delivery of multiple global trials through full DM life-cycle (i.e. large trials of at least 1000 patients). Demonstrated expert data management skills and advanced knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation, management of local laboratory data, and/or new technology). Previous experience and proven competence in handling complex customer negotiations and bid defense meetings independently. Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology. Knowledge of operating procedures and work instructions and the ability to apply them in practice. Knowledge of Good Clinical Practices and relevant regulatory guidelines. Excellent communication, interpersonal, customer service, and teamwork skills. Excellent organizational and problem-solving skills. Excellent project management skills. Ability to work independently. Comprehensive understanding of clinical drug development process. Ability to establish and maintain effective working relationships with coworkers, managers and customers. Previous experience and proven competence in managing delivery of multiple global trials through full DM life-cycle (i.e. large trials of at least 1000 patients). Demonstrated expert data management skills and advanced knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation, management of local laboratory data, and/or new technology). Previous experience and proven competence in handling complex customer negotiations and bid defense meetings independently. Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology. Knowledge of operating procedures and work instructions and the ability to apply them in practice. Knowledge of Good Clinical Practices and relevant regulatory guidelines. Excellent communication, interpersonal, customer service, and teamwork skills. Excellent organizational and problem-solving skills. Excellent project management skills. Ability to work independently. Comprehensive understanding of clinical drug development process. Ability to establish and maintain effective working relationships with coworkers, managers and customers. 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.

Duties/Responsibilities: Act as signal detection and literature lead, or back-up lead to contribute to the conduct of ongoing literature safety surveillance for marketed and investigational products, evaluating      events of special interests as well as aggregate data reviewAuthor and finalize aggregate reports, including but not limited to PBRERs/PSUR, DSURs and ACOs.Author responses to regulatory agency/ Pharmacovigilance Risk Assessment Committee (PRAC) inquiries, as required.Can serve as principal owner (molecule lead) for the molecule and have responsibility for completion of the deliverable and in compliance with all applicable Key performance indicators (KPI); Set-up and update products' signaling strategies, as approved by the customer’s Safety Strategy Lead. Author and/or QC review all types of signal management deliverables. Lead/ conduct ongoing signal detection activities as per agreed signaling strategies, perform signal validation and signal evaluation analyses for proactive and timely identification of signals and characterization of risks, as approved by the customer’s Safety Strategy Lead. Responsible for full documentation and tracking of signals.Ensuring the completion of molecule deliverables on time and liaise with portfolio clinical science scientists, service provider process leads and cross-functional stakeholders.  Distribution of molecule work within team consisting of molecule scientists, when necessary, coordinating support across molecules and disease areas when there are peaks and troughs in workload.End-to-end molecule work oversight and responsibility (i.e., ensuring consistent tracking of signals from detection to assessment to inclusion in aggregate reports).Ensuring an in-depth knowledge of the molecule and disease area within the service provider molecule team.Oversight and responsibility of quality-of molecule deliverables to the customer’s molecule team, with “hands-on” involvement, i.e., involved in authoring DSR conclusion, participating in SD/Lit meetings between service provider and customers.Responsible for resolution of issues on molecule deliverables (if necessary, in collaboration with service provider process lead).Participate in internal and external audits and inspections, as required.Read, acknowledge and adhere to all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion to maintain compliance and documentedConduct regular lessons learned with the working teams to ensure all information from the customer is cascaded to the relevant team members.Qualifications: Life science graduate/post-graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance4-6 years of relevant experience in Pharmacovigilance including hands-on experience of drug safety, aggregate reports, signal detection/signal management preferredExcellent communication (written and verbal) skillsTeam workingEnglish – fluent (spoken, written)IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Candidates must reside in the same country where the role is located Overview The Commercialization Partner - Emerging Biopharma (EBP) is a trusted advisor to IQVIA’s EBP clients, incorporating deep expertise in commercialization and launch to support the development, enablement and execution of their commercialization strategies.  The Commercialization Partner will utilize the full spectrum of IQVIA’s resources to develop complex integrated solutions that enable successful commercialization strategies and first-in-class delivery for EBP clients across therapeutic areas in the United States.  The Commercialization Partner will: Develop and deliver insightful, value-added commercialization strategies that address complex EBP client needsBuild trusted partner status via deep commercial content expertise, act as a thought leader for clients and delivery teams Conduct strategy sessions with clients to outline an integrated commercial launch plan, with regular check-ins to assess progress and address questionsLeverage prioritization frameworks to focus pre-commercial team effort on accounts that are likely to launch on their own and provide IQVIA a positive engagement return-on-investmentPrepare analytical proof points and recommendations for launch critical success factors aligned with IQVIA’s proposed client solutions and launch perspectivesLead senior level meetings with clients to support launch planning, market, and therapy area insights, and overall solution design and rationaleAct as principal owner of client engagements; ultimate responsibility for client satisfaction and delivering high levels of quality/added valueCreate and elevate new business opportunities through the identification of value-added follow-on work and identify new revenue opportunities with existing and new client organizationsMentor, coach, and share subject matter expertise with others to help develop individuals and capabilities delivering world-class solutions for clientsQualifications: Bachelor’s degree required, Master’s degree preferred10+ years’ experience in life science or consulting industry required, preferred 3+ years’ experience with IQVIA and its offerings, experience in product development, analytics, and strategy highly preferredDemonstrated biopharmaceutical forecasting and deal modeling skills; deep knowledge of the steps and processes required to successfully launch biotechnology products Ability to speak in detail with EBP client C-suite leaders about brand, launch and commercial strategy services/solutions, specifically in the life sciences industry segment, in a meaningful manner with depth of content knowledge.Proven ability to build relationships, identify client pain points, and develop custom solutions, providing comprehensive and authoritative knowledge in brand/commercial services solutionsKnowledge of industry, client and competitive trends in the life sciences industry. Ability to apply this knowledge to both active client engagements and business/client development activities.Strongly prefer an in-depth understanding of IQVIA’s data assets, analytical tools and IQVIA core offerings Demonstrated ability to express ideas in a clear and concise manner; tailor message to target audiences with the gravitas to build long-lasting relationships. Experience in leading functional teams in the capture of internal/external client/project requirementsConsultative mindset with enthusiasm for delivering first-in-class solutions to clients; demonstrated strategic thinking, planning and change management skillsWork location is flexible and may be remote or based in a US IQVIA office location. 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 $168,600.00 - $469,900.00. 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.

Health Information Technology Specialist  Do you have a passion for harnessing technology to make a positive impact on patients’ lives? Do you have Electronic Healthcare Record (EHR) experience and are looking for a rewarding career path within the Health Information Technology field? We are excited to announce that currently we are looking for Health Information Technology Specialists to support an IQVIA pharmaceutical client partnership This individual will have the unique opportunity to be a part of multiple cardiovascular brands in the US market as a Health Information Technology Specialist. The primary focus of this role will be to support integration of the brand into EHR systems across priority accounts, helping identify and address barriers that affect patient care, access, treatment processes, patient identification, and overall end-user experience In addition, the Health IT Specialist will be responsible for sharing Electronic Health Record insights to enhance patient care and support population health approaches across both in-patient and outpatient sites of care at priority accounts. Other responsibilities include developing and implementing comprehensive customer specific plans, as well as working in a collaborative manner with Account Management, Medical and Cross functional account teams The Health IT Specialist will also support healthcare stakeholders including end users, clinicians, informatics, Quality, Population Health and IT teams. Success in this position requires a self-starter that thrives in ambiguity and can be both a strategic partner and outcomes driven.  Core Duties/Responsibilities: Health IT Specialist Identify potential gaps/barriers within EHR systems at priority IDN’s & Health SystemsProblem solve and provide solutions and resolution of EHR gapsIdentify workflow barriers and recommend scalable solutionsWorks collaboratively with customers including end users, licensed clinicians, IT informatics team, quality EHR Manager and analyst to provide meaningful insights to enhance patient careAlign resources to develop comprehensive plans by priority institutionComplete workflow assessments with institutional customers to identify potential gaps in care across the patient journeyDevelop and implement comprehensive customer specific plansWill act as matrix team Health IT Specialist subject matter expert to both internal and external stakeholders with matrix partners across account management, medical, and other cross functional partners. TShare insights around optimizing EHR systems to address gaps in patient care including Inpatient, Outpatient, and Emergency Department Requirements Bachelor's degree from an accredited college/university required;Minimum of 4 years working in design, build, and/or testing expertise and experience with EHR software, including: Epic, Cerner, Meditech, McKesson preferred; and/or within a Health System informatics group or team at leadership level, or similar role within a pharmaceutical company.In depth knowledge of healthcare and health information technology, and software build, and/or optimization techniquesAbility to discover issues, prioritize and problem solve to resolution Team player with the willingness/ability to work in a matrix environmentExcellent presentation skillsStrong oral and written communication skillsEnthusiastic, positive attitude, flexibilityAbility to consistently travel overnight Preferred Master’s degreeClinical IT experience, Pharmacy IT, or Nursing InformaticsPharmaceutical or Life Science Health IT Specialist experienceB2B or software sales experience#LI-CES IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is $125,000 - $135,000 annually. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

We are seeking a motivated and results-driven Pharmaceutical Sales Representative to join our team. In this role, you will be responsible for driving volume and market share growth for assigned pharmaceutical products within a designated territory. You will build strong relationships with healthcare professionals and deliver impactful sales presentations in an office-based setting. Key Responsibilities Include: Generating volume and market share growth for assigned pharmaceutical products within a specific geographic area. Selling presentations to physicians and other health care professionals, primarily in an office-based setting. Developing an understanding of the issues and opportunities unique to the geography, particularly in managed health care. Manage allocated resources (samples, promotional and educational materials) to maximize return within regulatory and ethical guidelines. Maintains accountability for all pharmaceutical samples in accordance with FDA and PDMA guidelines. Utilize the sales automation system to document call and program activity. Complete initial and ongoing product and development training as required.Requirements: BA/BS requiredPreferred: Minimum of 2 years business-to-business outside sales experience with demonstrated record of impact preferred. 1-2 years of Pharmaceutical Sales experience with demonstrated record of impact preferredEstablished relationships within targeted geography.Key Competencies: Sales ability/persuasiveness, use of appropriate interpersonal style and communication methods to facilitate an acceptance of an idea, plan, activity or product from targeted customers.Establishes account plans based on customer needs and business priorities.Establishes method for monitoring progress to goals.Must set high goals or standards of performance, self-starter, able to work independently.Must demonstrate ability to influence events to achieve goals and take actions beyond what is required in being proactive.Must be able to utilize resources and create a positive/professional impression, commanding attention and respect, displaying confidence.Ability to maintain effectiveness in varying environments and with different tasks, responsibilities and people is key.Must express ideas effectively in individual and group situations, adjusting to the characteristics or needs of the target audience#LI-CESIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is $85,000 - $115,000 annually. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Field Sales Associate – UrologyAbout the Role As a Field Sales Associate (FSA) at Boston Scientific, you will play a pivotal role in supporting regional accounts under the guidance of the Region Sales Manager. Working closely with Territory Managers, you’ll help maintain market share across existing accounts while delivering exceptional service and clinical support. This includes conducting in-services and assisting with training initiatives to elevate the team’s performance and customer experience. Key Responsibilities Strengthen key account relationships through regular customer visits, product demonstrations, educational programs, in-services, procedural observation, and issue resolutionEngage with a broad range of stakeholders including physicians, nurses, technicians, materials management, hospital administration, and infection controlCollaborate with Territory Managers, Sales Management, HEMA, and cross-functional teams to assess business conditions and sales trendsDrive utilization of targeted technologies across assigned accountsDemonstrate clinical excellence in relevant disease statesDevelop and execute proactive service plans with the Region Manager and team to maintain market share and enhance customer satisfactionSupport professional education initiatives by participating in on-site and field training workshopsIdentify opportunities to present Boston Scientific solutions that drive regional sales activityProvide timely updates to the Regional Manager on business plans, competitive landscape, and industry trendsManage expense and promotional budgets in accordance with company guidelinesPrepare comprehensive account-level plans aligned with the Urology Division’s strategic goalsLeverage sales enablement tools such as Salesforce and Tableau to optimize performanceMaintain accurate records of expenses, customer interactions, and field reportsSubmit all required administrative documentation promptlyConduct all sales activities in compliance with Travel & Entertainment (T&E) guidelines, AdvaMed policies, and company integrity standardsParticipate in occasional weekend and evening trade shows or meetingsCommit to travel requirements, typically 40–50%Preferred Qualifications Self-starter with strong leadership qualities and high coachabilityProven ability to set priorities and manage time effectivelySkilled in building and maintaining customer relationshipsFlexible and adaptable to change; able to align work with strategic goalsEnergetic, enthusiastic, goal-oriented, and determinedThrives in a fast-paced, competitive environmentRequired Qualifications Minimum 1 year of successful B2B sales experienceCompletion of a formal sales training program or relevant degreeBachelor’s degreeMust reside within the assigned territoryNote: This role is not eligible for visa sponsorship. Candidates must have authorization to work in the US without the need for sponsorship.#LI-CESIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is 70-75,000 annually. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job Overview Under appropriate guidance, ensure that personal administration and HR processes are executed in-country in full compliance with local labor legislation, Core HR standards, and corporate policies. Key Responsibilities: With limited guidance, deliver comprehensive HR support to employees and managers across assigned service areas, business units, or functions. Independently manage HR-related inquiries and collaborate with senior HR team members and line management as required to address complex issues. Manage employees in accordance with organizational policies and applicable employment laws, including responsibilities related to hiring, terminations, sick leave/absence administration, maintenance of personnel files and HR documentation, proactive tracking of expiring contracts, employer statements and references, operational support for local HR communications/intranet content, and employee relations matters. Build and maintain strong, effective working relationships with HR specialist functions and Centers of Excellence, including HR Shared Services Tier 1, HR Business Partners, Payroll, and Benefits teams. Support line managers, as appropriate, in the delivery of new employee orientation and onboarding activities. Conduct ad hoc reviews as directed and provide recommendations on employment legislation, compliance, HR systems, practices, and procedures; support and educate line management with appropriate guidance. Partner with senior HR team members on organizational effectiveness and change management initiatives related to reorganizations, mergers and acquisitions, and employee transfers, ensuring compliance with local legislation. Participate, with minimal supervision, in the day-to-day development and implementation of local and global HR initiatives, including redesign and transformation efforts. Prepare and deliver HR reports and analyses as requested by senior management. Actively contribute to continuous improvement initiatives to enhance service quality, exceed customer expectations, and promote a professional HR organization. Scope of responsibility: Netherlands. Qualifications: Bachelor’s degree required. Fluency in Dutch and English. 2–4 years of experience in an HR function or in personnel administration processes; prior experience in an HR Shared Services environment is an added advantage. Proficiency in Microsoft Office applications; experience with Workday and DocuSign is considered an advantage. Demonstrated ability to exercise sound judgment within established procedures and practices to determine appropriate actions. Proven ability to prioritize and coordinate multiple work requirements to meet deadlines effectively. Ability to establish and maintain effective working relationships with colleagues, managers, and internal clients. Strong knowledge of local and relevant employment legislation. Excellent verbal and written communication skills, with strong interpersonal capabilities. Ability to work effectively both independently and as part of a team. Strong attention to detail and the ability to operate successfully within a matrixed organizational environment. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

About the RoleIQVIA is seeking a talented and motivated Primary Market Research Consultant to join our team in Algeria. In this role, you will support the design, management, analysis, and delivery of primary market research projects across the pharmaceutical and healthcare sectors. Working closely with clients, project leaders, and cross-functional teams, you will contribute to generating actionable insights that help healthcare organizations make informed strategic and commercial decisions. Key ResponsibilitiesDesign and develop market research questionnaires and discussion guides for quantitative and qualitative studies.Manage market research projects in collaboration with internal IQVIA teams and external partners.Ensure projects are delivered on time and within scope while providing regular status updates to clients and stakeholders.Develop report templates and define data tabulation requirements to support analysis and reporting.Review outputs produced by offshore teams and conduct preliminary analysis to identify key findings, trends, and insights.Create high-quality client presentations and support the design and coordination of interactive dashboards where required.Conduct ad-hoc analyses using raw data to address client questions and support follow-up requests.Build expertise in healthcare consulting, pharmaceutical markets, and market research methodologies through project work and continuous learning.Contribute to the development of innovative approaches and best practices within the team.Qualifications & ExperienceRequiredBachelor's or Master's Degree in Life Sciences, Pharmacy, Medicine, Economics, Business, Mathematics, Statistics, or a related field.Minimum 5 years of experience in healthcare or pharmaceutical market research.Proven experience designing and managing quantitative and/or qualitative market research projects.Strong analytical and problem-solving skills with excellent attention to detail.Ability to interpret data and translate findings into actionable insights.Experience working in a client-facing environment and managing multiple projects simultaneously.Proficiency in Microsoft Excel, PowerPoint, and Word.Strong communication and stakeholder-management skills.Ability to work effectively in a collaborative, multicultural environment.PreferredExperience within the pharmaceutical, healthcare, consulting, or market research industries.Familiarity with the Algerian healthcare and pharmaceutical market.Experience with dashboarding and data visualization tools.LanguagesFluent English required.Fluency in French required.Arabic is an advantage.What We OfferOpportunity to work on strategic projects with leading healthcare and pharmaceutical organizations.Exposure to regional and international markets.Professional development and continuous learning opportunities.Collaborative and inclusive work environment.Career growth within a global healthcare and life sciences organization.Location: Algeria (Algiers preferred) IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Clinical Research Coordinator in York Working Hours: 24 hours per week Start Date: ImmediatelyDuration: Approximately 6 months IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in York. This part-time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment. Key Responsibilities As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks, including: Prescreening and Screening tasksReview charts from the site data baseMaintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systemsSupporting patient screening and enrollment, including handling informed consent and privacy documentationCoordinating logistical activities for study procedures in line with the study protocolProcessing lab samplesPerforming data entry, quality checks, and resolving queries to ensure data accuracy and completenessPatient educationCommunicating with study monitors and responding to study-related inquiriesCarrying out general administrative tasks related to the studyYour ProfileWe are looking for candidates who bring a combination of education, experience, and skills: Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedulesGood knowledge of medical terminologyStrong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)Must have at least 2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial siteExcellent interpersonal and communication skillsStrong organizational skills and attention to detailFluency in EnglishWhy Join IQVIA?At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference. Interested?If this sounds like the right opportunity for you, we encourage you to apply today. Please note we cannot offer sponsorship for these positions. #LI-HCPN #LI-CES #LI-DNP #LI-CT1 #LI-Onsite IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Responsibilities: Conducting thorough research and staying abreast with the latest developments on medical front in the allocated therapeutic area, ensuring that the curated content is current and relevant to the audience as well as client interest.Utilizing apt tools for editing the articles, leveraging the platform’s tools to create visually engaging, concise and coherent infographics that effectively convey key findings from the researched articles for optimized readability.Collaborating with the subject matter experts to refine the infographics, ensuring accuracy, clarity and adherence to industry standards, before finalizing the visual content.Managing the scheduling of review and posting process, ensuring timely publication of the content on the platform.Qualifications Desired TA knowledge: Including but not limited to – Oncology and rare diseases, Cardiovascular, Nutrition, Vaccines.  Bachelor's/Master's Degree /Ph.D in life sciences related discipline or related fieldTypically requires 1-3 years of prior relevant experience and related competency levels.Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner.In depth knowledge of drug development, medical writing, and associated regulations. Good understanding of statistical principles and of medical terminology across a range of therapeutic areas.Excellent written and oral communication skills including grammatical/technical writing skills.Excellent attention to detail and accuracy.Communicates clearly, effectively and confidently with others.Demonstrated abilities in collaboration with others and independent thought.Demonstrates confidence and maturity in most routine medical writing situations.Demonstrates good judgement in requesting input from senior staff.Ability to establish and maintain effective working relationships with coworkers, managers and customers.Ability to effectively manage multiple tasks and projects.Must be computer literate.#LI-CES#LI-PK1#LI-DNP  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Product Manager – Data ProductsRole Overview We are seeking a strategic and customer-focused Product Manager to lead the vision, roadmap, and delivery of data products that drive business value and innovation. This role will partner closely with engineering, analytics, and business stakeholders to develop scalable data solutions, prioritize investments, and ensure successful product outcomes. The ideal candidate combines strong product management expertise with a solid understanding of modern data platforms and infrastructure. Key ResponsibilitiesBuild and execute a product roadmap that delivers incremental value and drives the achievement of clearly defined business objectives.Develop strong cross-functional relationships, earning the trust and respect of stakeholders, engineering teams, and business partners.Contribute to product strategy and make informed trade-off decisions based on business priorities, market dynamics, customer needs, and technical considerations.Understand market, industry, and customer requirements and translate them into product features, capabilities, and use cases.Apply best-practice product management methodologies to drive a product-led approach to prioritization, solution design, and execution.Lead product discovery efforts to improve predictability, maximize ROI, and ensure investments are aligned with business outcomes.Partner with engineering and data teams to ensure products are scalable, reliable, secure, and well-supported.Support product launches, stakeholder communications, product marketing, and sales enablement through effective coordination, documentation, and presentations.Drive adoption and continuous improvement by gathering user feedback, monitoring performance metrics, and identifying opportunities for enhancement.Desired Experience & SkillsStrong product management experience with a track record of delivering impactful digital or data-driven products.Data product leadership experience strongly preferred, including ownership of data platforms, analytics products, reporting solutions, or data services.Understanding of data modeling, data pipelines, Snowflake infrastructure, and API design is highly desirable.Familiarity with Atlassian Confluence and Jira for product planning, documentation, and agile delivery.Experience working in Agile/Scrum environments and collaborating with technical and non-technical stakeholders.Strong analytical, problem-solving, and communication skills.Ability to translate complex technical concepts into clear business value propositions.QualificationsBachelor's Degree in Computer Science, Information Systems, Engineering, Business, or a related field, or equivalent practical experience.Experience managing technical, data, or platform products in a fast-paced environment.Demonstrated ability to balance customer needs, business goals, and technical feasibility while delivering measurable outcomes.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is zł160,200.00 - zł297,300.00. 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.

Country Activation and Submission Representative IQVIA Biotech📍 Poland | Home-Based About IQVIA BiotechAt IQVIA Biotech, we partner with innovative biotech companies to help transform scientific discoveries into life-changing therapies. Through dedicated teams, therapeutic expertise, and a biotech-focused delivery model, we support clinical development from early-phase studies through global registration programs. We are currently seeking a Country Activation and Submission Representative  to join our Site Activation team in Poland. Role OverviewAs a Country Activation and Submission Representative , you will be responsible for managing country-level regulatory and site activation activities across clinical studies in Poland. You will support studies from initial submission through study maintenance and close-out activities, working closely with investigative sites, project teams, and regulatory authorities. This role requires strong knowledge of the Polish regulatory environment, EU Clinical Trial Regulation (EU CTR) submissions, and site activation processes. Key ResponsibilitiesManage EU CTR submissions in Poland, including both initial submissions and amendments.Coordinate and oversee regulatory and site activation activities from study start-up through study maintenance and study end.Prepare, review, compile, and maintain Essential Document Packages (EDP).Manage country-specific Informed Consent Form (ICF) adaptations and related documentation.Act as the primary contact for investigative sites throughout the study lifecycle.Build and maintain strong relationships with sites through proactive communication and support.Prepare and submit regulatory documentation in accordance with local requirements and project timelines.Review, track, and follow up on approvals from regulatory authorities and ethics committees.Respond to and coordinate Requests for Information (RFIs) from Regulatory Authorities.Ensure all regulatory and site documents meet quality standards and compliance requirements.Support Site Activation Managers and project teams by providing local regulatory expertise and timeline guidance.Manage studies in both start-up and maintenance phases simultaneously, ensuring deliverables are completed on time.Participate in feasibility activities and support site identification processes.Contribute to site contract negotiations and feasibility assessments (preferred but not mandatory).Required QualificationsBachelor's Degree in Life Sciences or a related field.Experience within clinical research, with a focus on study start-up, regulatory affairs, or site activation activities.Hands-on experience with EU CTR submissions in Poland.Experience preparing and managing Essential Document Packages (EDPs).Understanding of Polish regulatory and ethics submission requirements.Experience handling initial submissions and amendments.Experience communicating directly with investigative sites and coordinating site activation activities.Ability to manage multiple studies and priorities simultaneously.Strong organizational and project management skills.Solid understanding of ICH-GCP guidelines and clinical trial regulations.Excellent verbal and written communication skills.Fluency in Polish and English.Preferred QualificationsExperience responding to Regulatory Authority RFIs.Experience supporting study maintenance activities in addition to start-up.Exposure to site feasibility activities.Contract negotiation experience.Experience working within a CRO, biotechnology, or pharmaceutical environment.What You'll BringStrong attention to detail and quality-focused mindset.Ability to work independently in a remote environment.Effective stakeholder management skills.Strong problem-solving and organizational abilities.Capability to build collaborative relationships with sites, sponsors, and internal teams.Why IQVIA Biotech?Opportunity to work with innovative biotech sponsors developing next-generation therapies.Home-based flexibility in Poland.Exposure to global and regional clinical development programs.Collaborative, supportive, and growth-focused environment.Career development opportunities within a world-leading clinical research organization.Join IQVIA Biotech and help accelerate the delivery of innovative treatments to patients worldwide. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is 151.200,00 zł - 280.700,00 zł. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Join IQVIA as a CRA 1 (m/w/d) in our Clinical Site Management department home-based throughout Austria. You will focus on a comprehensive clinical trial management in a variety of indications and learn about the diverse scientific approach of the sponsors. Beside establishing strong relationships with the global study team and the involved investigators, you will conduct monitoring on complex clinical trials for different pharma companies and assure their adherence to good clinical practices and study protocols. With strategic site relationship managers supporting you throughout your role, this is a fantastic opportunity for you to embed yourself in the wider clinical operations team and work on ground-breaking new medicine development. Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits. Supporting the development of a subject recruitment plan. Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution. Collaborating with experts on study sites and client representatives. Qualifications: University Degree in life science or other scientific discipline or apprenticeship in health care. Experience as CRA, Study Coordinator/Nurse or Clinical Trial Coordinator is required Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment. Good command of German and English. Flexibility to business travel up to 70% of working time. Driver’s license class B. What you can expect: Resources that promote your career growth. Leaders that support flexible work schedules. Programs to help you build your therapeutic knowledge. Dynamic work environments that expose you to new experiences. Home-office, company car, accident insurance, pension and more. Monthly gross salary: starting at 4.000 EUR basic - an overpay according to skills and working experience is possible Whatever your career goals, we are here to ensure you get there! Please apply with your English CV and motivation letter. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

We are seeking Associate Scientist 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. Shift: Saturday-Wednesday, 4PM - 12:30 AM Job Summary: Perform routine laboratory testing and analytical procedures in a regulated environment. Ensure accurate documentation, data integrity, and compliance with SOPs and regulatory standards while supporting laboratory operations.  What You'll Be Doing: Perform and document analytical procedures in accordance with SOPs and regulatory guidelinesAnalyze routine laboratory data to ensure procedures are performing within acceptable tolerancesIdentify, document, and escalate deviations or atypical results to senior laboratory personnelPrepare samples, buffers, and solutions required for analytical testing activitiesSupport quality investigations, deviations, and corrective action processesMaintain, calibrate, and document laboratory equipment performanceAssist with onboarding and guide entry-level staff on routine laboratory proceduresCollaborate with cross-functional teams and communicate findings clearly and accurately What We Are Looking For: Bachelor's Degree or equivalent combination of education and experience6 months experience in a regulated laboratory environmentProficiency with relevant laboratory techniques and analytical methodsExperience working with laboratory automation or specialized equipmentOther equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role: Strong attention to detail and accuracy in laboratory documentation and analysisWorking knowledge of Good Laboratory Practices (GLP) and safety proceduresAbility to manage multiple tasks and collaborate effectively with internal stakeholdersProficiency in Microsoft Outlook, Word, and ExcelAbility to lift up to 50 lbs, frequent standing and walking, occasional sitting, close eye work requirement (computer, typing, reading small prints). Physical demands vary depending on assigned work area and work tasks. Occasional exposure to cold temperatures.  What We Offer You: We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey. To learn more about our benefits, visit https://jobs.iqvia.com/benefits. If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $41,400.00 - $86,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

We are seeking Pre-Analytical Services Assistant 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 Pre-Analytical Services Assistant supports the routine receipt and processing of clinical specimens in a laboratory environment. This role helps ensure shipments, specimen materials, and related documentation are handled accurately, safely, and in accordance with company procedures and applicable regulatory guidelines. What You'll Be Doing:Receive consignments and shipments and support routine specimen intake activitiesOpen shipments, review patient information forms, and escalate missing, incorrect, or damaged materials to senior staffDispose of or recycle kit shipping supplies according to established proceduresConduct secondary checks of shipping materials to ensure no specimens remain in packagingSupport after-hour alarms and other job-critical functions as neededAssist with equipment upkeep, supply inventory tasks, workstation cleanup, and general administrative dutiesOrganize the work area as requested by management and support safe, compliant daily operations What We Are Looking For:High School Diploma or equivalent requiredBasic computer skillsAbility to maintain effective reporting procedures and control workflowOther equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Strong attention to detail when reviewing shipment contents, specimen packaging, and patient information formsAbility to build and maintain effective working relationships with coworkers, managers, and clientsAbility to stay organized, follow safety procedures, and support workflow in a fast-paced laboratory settingWillingness to participate in continuing education through self-study and team meetingsAbility to lift up to 50 lbs, frequent standing and walking, occasional sitting, close eye work requirement (computer, typing, reading small prints). Physical demands vary depending on assigned work area and work tasks. Occasional exposure to cold temperatures. What We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.To learn more about our benefits, visit 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 $24,400.00 - $50,900.00. 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.