IQVIA

As Local Trial Manager (LTM) you will be responsible for running international/global studies in all therapeutic areas, managing the operational aspects of projects to meet contractual requirements. You will act as primary point of contact in Belgium to lead, manage and co-ordinate the conduct of clinical trials from study start-up (COLA) to close out at a country level in accordance with ICH-GCP and other applicable local regulations. RESPONSIBILITIES OVERVIEW   ·       Partner with global, local country teams and study team to provide high level country strategy, drive study progress and country level study delivery. (Accountable for study deliverables and drives key decisions within set country) ·       Plan, manage, and maintain oversight of clinical study execution in accordance with the global program strategy, through leadership of the cross-functional Local Study Team (LST) ·       Support country-level operational planning and accountable for site selection within assigned country(ies) ·       Contribute and develop to program,/study-specific materials – e.g., monitoring plan, study specific training documents. ·       Accountable for site-level goal setting and study-specific deliverables for clinical sites within their country(ies) ·       Contribute to, deliver and/or lead CRA, Investigator and Study Coordinator training ·       Oversight and monitoring of applicable vendor activities e.g., laboratories and equipment provisioning ·       Contribute to the study-level forecast for investigational product, support study level accountability and reconciliation across assigned countries, management of ELE (enrolment long-range estimates) process ·       Monitor the execution of the clinical study against timelines, deliverables, and budget for that country: ·       Monitor and review country and study trends, Review Monitoring Visit Reports ·       Identify and facilitate resolution of cross-functional study-specific issues ·       Provide updates regarding the study budget and obtain approval for budget deviations for clinical sites (outside of range) ·       Conducts on-site quality visits with CRAs where/when appropriate and supports the maintenance of investigator site relationships.   REQUIRED EDUCATION AND EXPERIENCE   ·       Bachelor’s degree in a healthcare or other scientific discipline ·       Minimum 2-3 years’ experience of leading local/regional or global teams ·       Minimum 2-3 years’ clinical trial project management experience ·       Experience in oversight of external vendors (e.g., CROs, central labs, imaging vendors, etc.).   REQUIRED KNOWLEDGE   ·       Local knowledge / expertise of regulatory environment, study start up process and associated timelines etc. ·       Clinical trial processes and operations ·       Extensive knowledge of ICH/GCP regulations and guidelines ·       Project and Program management including oversight of study deliverable, budgets and timelines ·       Time, cost and quality metrics, Key performance indicators (KPIs) ·       Fluent in French, Dutch and English is essential. ·       Availability to travel occasionally across the country. 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 – Measurement Studies, Platforms & Data ServicesLocation: RemoteJob Type: Full-timeJob OverviewIQVIA Digital Overview:IQVIA Digital powers exceptional brand experiences, delivering innovative solutions based on a customer-first, insights-driven, and integrated omnichannel vision. We provide authenticated, privacy-enhanced data and analytics, innovative fit-for-purpose healthcare technology, and the expertise to enable an effective and adaptable marketing model that drives better quality of care and patient outcomes. IQVIA is the leading global provider of data, advanced analytics, technology solutions and clinical research services for the life sciences industry. Learn more at www.iqviadigital.comThe Product team is responsible for defining and executing the vision, strategy, and roadmap for IQVIA Digital's portfolio of data, technology, and media solutions. Through close partnership with clients and cross-functional collaboration with Go-to-Market, Technology, Data Management, and Operations teams, the team translates market insights and customer needs into innovative, scalable products. Built upon IQVIA's industry-leading healthcare data assets and privacy-by-design foundation, these solutions deliver differentiated value to clients, drive business growth, and advance IQVIA Digital's leadership in the healthcare marketing ecosystem.IQVIA is seeking a Product Manager – Measurement Studies, Platforms & Data Services to support and help advance our Measurement Studies and Platform offering. This role will focus on enabling IQVIA’s measurement value proposition through measurement study reporting, platform delivery, and data-as-a-service integrations across HCP and DTC measurement capabilities.The Product Manager will manage a defined area of the measurement portfolio and apply portfolio-level thinking to ensure product initiatives align with a cohesive, scalable, and client-focused measurement product strategy. This role will help bring IQVIA’s measurement capabilities to life by maximizing client value, streamlining offerings, and supporting continued business growth.As part of the Measurement team, this individual will work across healthcare verticals with healthcare marketers, publishers, agency partners, advertiser clients, and channel partners. The role requires close collaboration with Platform, Science & Innovation, Data Management, Sales, Product Strategy, Marketing, and client-facing teams to identify market needs, shape product direction, and deliver solutions that support adoption and measurable value.Key ResponsibilitiesContribute to the product strategy and roadmap for existing and new measurement product offerings, ensuring alignment with strategic business objectives.Manage a defined portion of the measurement portfolio and support prioritization of initiatives based on client value, revenue potential, and opportunity-cost considerations.Partner closely with Sales teams and clients to support revenue growth, client engagement, and product adoption.Own product prioritization, functionality, and scope definition to deliver value to customers while ensuring excellence in product delivery.Support key measurement areas, including:DTC and HCP measurement studies, including digital media, TV, cross-channel, attribution, and related solutions.DTC platform and BI reporting capabilities.Data-as-a-Service offerings.Build strong partnerships with internal teams to identify, assess, and advance new go-to-market opportunities and product offerings.Oversee the product lifecycle from concept through launch, sales support, and ongoing enhancement based on customer feedback and market needs.Incorporate best practices in methodology, data visualization, and end-user experience into product requirements and feature definition.Collaborate with product teams to support consistent measurement standards and a unified client experience.Manage and support two Product Owners, ensuring alignment on priorities, delivery expectations, and stakeholder communication.Engage directly with key client stakeholders across healthcare verticals to understand business needs and translate insights into scalable product solutions.Partner with Measurement Product Strategy and Marketing to support product positioning, messaging, and go-to-market readiness.Stay current on industry trends, competitive landscape, and emerging technologies through ongoing market research.Navigate data privacy, security, and regulatory requirements, ensuring compliance considerations are incorporated into product design and delivery.QualificationsBachelor’s degree in Statistics, Analytics, Business, or a related field required; advanced degree preferred.10+ years of product management experience, preferably within healthcare, data-driven, or technology-focused organizations.Strong understanding of the digital media and measurement landscape, including digital marketing data, marketing technology, and advertising technology.Knowledge of key players across healthcare, publishers, DSPs, SSPs, and ad tech ecosystems.Experience working with IQVIA or clinical data sets preferred.Proven ability to deliver against objectives and timelines through roadmap planning, prioritization, and execution.Experience creating go-to-market materials, including product positioning and pricing.Strong communication, stakeholder management, and cross-functional collaboration skills.Ability to support internal and external stakeholders while translating business needs into practical product solutions.Proficiency in advanced measurement methodologies and attribution preferred.Strategic thinker with strong analytical skills, innovation mindset, and results-driven approach.Revenue-focused mindset with experience supporting measurement sales and revenue-generating product initiatives.Preferred Skills and ExperienceHealthcare, life sciences, digital media, or measurement product experience.Experience supporting platform-based reporting, BI tools, or data-as-a-service solutions.Ability to work with cross-functional teams in a matrixed environment.Strong understanding of data privacy, security, and regulatory considerations within healthcare or data-driven product environments.Demonstrated ability to balance client needs, business priorities, technical feasibility, and revenue impact.What You Will BringThe successful candidate will bring a strong product management foundation, a deep understanding of measurement and data-driven solutions, and the ability to translate client and market needs into scalable product offerings. This individual will be comfortable working across teams, influencing stakeholders, supporting revenue growth, and helping shape product strategy within a fast-evolving healthcare technology 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 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 $88,100.00 - $220,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA's AI and Technology Solutions (ATS) organization is hiring five Principal Enterprise Architects to define and govern enterprise-wide architecture strategy, standards, and roadmaps across a large, global technology landscape, with particular emphasis on clinical operations and clinical trial management domains. The role sits in the Architecture & Standards (A&S) group and works in close partnership with business, technology, and product leadership to translate strategy and OKRs into standards-driven, scalable enterprise architectures that reduce technical debt, promote reuse, and align to "the IQVIA way."  Critical to success is deep familiarity with clinical operations and clinical trial management domains, including understanding of study design, site and patient management, regulatory compliance workflows, data integration across clinical and operational systems, and how technology and AI/agent-based capabilities can be applied to optimize trial execution and Clinical Operations efficiency.   Preference will be given to candidates with hands-on experience in clinical trial management, site operations, patient cohort management, or related clinical domains, combined with ability to use enterprise architecture tools and capability models as the stable backbone for processes, products, data, and automation across business units.  Job overview  The Principal Enterprise Architect is accountable for co-designing target-state enterprise architectures and reference models with business, technology, and product leaders, and for prescribing standards, patterns, and guardrails that ensure consistency and scalability across IQVIA. The role provides a portfolio-wide view of business and technical capabilities, surfacing cross-cutting needs and opportunities to consolidate platforms and services in both application and data domains. Within clinical operations and clinical trial management, the architect will establish patterns and standards that govern how data flows across trial planning, site activation, patient recruitment, data collection, and trial closeout workflows, ensuring that technology investments support operational excellence and regulatory compliance.  Key responsibilities  Co-design and maintain enterprise architecture principles, standards, and reference architectures in partnership with business, technology, and product leaders, with explicit focus on clinical operations and clinical trial management to ensure that architecture patterns reflect the realities of study execution, site management, regulatory compliance, and patient safety.  Define target enterprise data, AI, and interoperability reference architectures, including standard patterns for event driven architectures (e.g., Kafka), API management (e.g., Apigee, Azure API Management, Kong), and AI/ML platforms (e.g., Azure ML, SageMaker), and ensure initiatives align to these standards and roadmaps. Within clinical domains, establish patterns for EDC integration, clinical data warehousing, site and patient data orchestration, and agentic AI for trial feasibility, site matching, and cohort discovery.  Partner with business units to translate strategies and OKRs into capability- and outcome-based architecture roadmaps that must with fully rationalized financials and an applied knowledge of, rather than project-specific solutions. In clinical operations, this includes collaborating with trial operations, site engagement, patient recruitment, and data management leaders to build roadmaps that optimize study start-up timelines, site activation efficiency, patient enrollment velocity, and data quality.  Provide an enterprise-wide view of interrelated business and technical capabilities, identifying patterns, shared needs, and reusable platforms and services. In Clinical Operations contexts, surface opportunities to consolidate disparate site management tools, EDC platforms, and patient data systems, and identify where agentic AI and automation can reduce manual operational burden.  Guide senior stakeholders through architectural options, trade-offs, and investment implications using clear, business-focused narratives and models. For clinical initiatives, articulate how architecture decisions impact trial timelines, regulatory risk, site partner experience, and patient enrollment.  Ability to translate clinical domain objectives (study, regulatory requirements, and site/patient operational constraints) into reusable capability models and architectural blueprints that enable consistent, scalable trial delivery across geographies and therapeutic areas.  Use enterprise architecture tools (e.g., LeanIX, Ardoq, MEGA) to define and maintain stable capability models and EA meta-models; map capabilities to processes, systems, products, outcomes, and key data domains; and support intake of new ideas into the enterprise roadmap through formalized architecture governance and portfolio intake processes and manage financial health across the portfolio In clinical domains, use capability models to organize trial operations (study design, site management, patient cohort management, data collection, compliance, closeout) and map them to technology investments and data flows.  Govern and rationalize the EA application and tooling portfolio, including inventories of business, data, and technology assets, and promote consistent adoption of standards across the organization. In clinical domains, rationalize point solutions and duplicate site/patient management tools; establish governance for new clinical technology investments to ensure alignment with reference architectures.  Collaborate with other business leaders, product managers, and domain architects and technology leaders to identify and mature shared services, platforms, and common patterns. Specifically, partners with clinical domain architects and product teams to evolve and standardize architectures for site engagement, patient recruitment, trial data management, and regulatory compliance automation.  Monitor technology and industry trends (especially AI/ML, data platforms, lake house governance patterns, life sciences tech, clinical trial innovation, and agentic AI applications in clinical workflows) and incorporate relevant innovations into enterprise standards and roadmaps. Track emerging capabilities in decentralized trials, wearable data integration, AI-driven patient matching, and agent-based workflow automation to keep IQVIA's Clinical Operations architecture competitive.  Mentor and influence architects and senior engineers to raise architecture maturity and adherence to enterprise standards across delivery teams. Develop coaching and reference architectures that enable clinical product and platform teams to build scalable, interoperable solutions aligned to enterprise standards.  Skills and Experience  15+ years in software development with 10–12+ years in enterprise architecture in large, complex organizations.  Demonstrated experience owning enterprise-wide technology strategies and roadmaps, including business architecture, value streams, capability maps, and customer journeys and apply financial acumen to ensure health of the portfolio  Recent, relevant enterprise experience with applied data science, AI/ML, and agentic AI solutions, including designing architectures for LLM-based and agent-based systems using technologies such as vector databases (e.g., Pinecone, Redis), orchestration frameworks (e.g., Lang Chain), and MLOps platforms (e.g., MLflow, Azure ML). Specific to clinical domains: hands-on experience with AI/ML applications in patient cohort discovery, site feasibility modeling, protocol complexity assessment, or operational forecasting for trial success.  Strong enterprise data architecture background, including implementation of data lakehouse architectures on platforms such as Databricks and Snowflake using medallion layering, plus data governance platforms and automation, data catalogs, ontologies, and taxonomies. In clinical contexts: demonstrated experience architecting clinical data warehouses, data warehouses, data integration, harmonized patient and site data models, and regulatory-compliant data governance for clinical trial data.  Deep, hands-on familiarity with clinical operations and clinical trial management, including study design, regulatory pathways, site activation and management, patient recruitment and cohort identification, workflows, protocol adherence monitoring, safety and pharmacovigilance reporting, and trial closeout and data archival. Preference for candidates with direct exposure to site partner needs, patient engagement challenges, and operational constraints that shape how technology can optimize trial delivery.  Experience in healthcare or life sciences, with a strong preference for working closely with clinical trial management, clinical operations, or related domains. Candidates should have directly supported Clinical Operations functions (site operations, patient recruitment, data management, regulatory compliance) and understand how technology architecture decisions cascade into operational efficiency, regulatory risk, and trial outcomes.  Deep understanding of modern architecture styles (event-driven, microservices-based, RESTful and alternative integration patterns, API-first) and how to codify them as enterprise standards and reference architectures. For clinical domains: ability to apply these patterns to site management workflows, patient data orchestration, and real-time trial monitoring dashboards.  Experience with both on-premises and cloud architecture on Azure and/or AWS.  Advanced proficiency with enterprise architecture tools (e.g., LeanIX, Ardoq, MEGA, or equivalent) and expertise in EA meta-models, capability modeling, portfolio management, data and application inventories, and architecture governance; demonstrated ability to design and operationalize EA meta-models that organize business capabilities, technology assets, data domains, and integration patterns at enterprise scale. For clinical applications: proven skill in building capability models that reflect trial operations, site partner experience, and patient journeys, enabling consistent translation of Clinical Operations strategy into technology roadmaps.  Soft skills should include strong executive presence, articulate communication and influence skills, collaboration, and tenacity with a track record of partnering with senior business, technology, and product leaders to drive adoption of standard-driven enterprise architectures at scale. Specifically, ability to engage clinical operations executives, site partners, patient advocates, and regulatory stakeholders to build consensus on architecture directions and demonstrate how technology investments drive operational and patient 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 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 $118,100.00 - $328,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

MCRA is part of IQVIA MedTech As a trusted CRO and advisory partner, IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together, we support innovation from concept to commercialization through regulatory, clinical, reimbursement, market access, and quality expertise. Position Overview  MCRA is seeking a Manager, Reimbursement, Health Economics & Market Access (RHEMA) to join its consulting team. The ideal candidate combines expertise in healthcare reimbursement, coding, medical record review, and reimbursement consulting to support medical technology clients. This role leads coding analyses, reimbursement assessments, client engagements, and strategic market access initiatives while providing project leadership and mentoring junior staff. Responsibilities and Duties Serve as a subject matter expert in reimbursement systems, coding methodologies, and clinical documentation. Lead inpatient facility and/or outpatient professional coding analyses using CPT, HCPCS, ICD-10-PCS, and ICD-10-CM. Conduct surgical coding audits and medical record reviews to evaluate coding accuracy, reimbursement implications, and compliance risks. Develop reimbursement, payment, coverage, and market access strategies based on coding and clinical findings. Manage client engagements, including project planning, timelines, budgets, quality, and deliverables. Prepare reports, presentations, coding analyses, and strategic recommendations. Present findings to physicians, providers, hospitals, and client stakeholders. Support payer and provider research and evidence-generation initiatives. Lead project teams and mentor junior consultants. Support business development, proposals, and thought leadership initiatives. Maintain expertise in reimbursement policy, coding guidance, and therapeutic-area trends. Required Qualifications Bachelor's degree in Health Information Management, Nursing, Life Sciences, Public Health, Health Administration, Business, or related field. Typically 5–10 years of inpatient facility and/or outpatient professional coding experience plus reimbursement, consulting, market access, provider strategy, or revenue cycle experience. Advanced knowledge of CPT, HCPCS, ICD-10-PCS, ICD-10-CM, medical record review, and surgical coding audits. Current AAPC or AHIMA certification (e.g., CPC, CCS, CCS-P, RHIA, RHIT). Strong analytical, communication, presentation, project management, and client management skills. Proficiency with Microsoft Office applications. Preferred Qualifications Advanced degree in a related field. Additional specialty coding credentials. Experience translating coding analyses into reimbursement and market access strategies. Experience presenting to physicians and provider organizations. Work Environment Professional office or remote work environment with occasional travel for client meetings, conferences, and internal meetings. NOTE: This job description is not intended to be all-inclusive. Employees may perform other related duties to meet the ongoing needs of the organization. MCRA, LLC is an equal opportunity/Affirmative Action employer and does not discriminate in its selection and employment practices. 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 $95,700.00 - $239,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Are you interested in collaborating with leading pharma companies to help patients all around the world? When you join IQVIA as a sponsor-dedicated Senior CRA in Poland, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether you're just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development. With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas. Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionCollaborating with experts at study sites and with client representativesDepending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices)  Qualifications: University Degree in life science or other scientific discipline or apprenticeship in health careMinimum of 3 years of on-site monitoring experience, alternatively an equivalent combination of education, training and experienceStrong experience in monitoring of clinical trialsKnowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesStrong written and verbal communication skills, attention to detail and ability to work in a fast pace environmentGood command of Polish and English languageFlexibility to travelWhat you can expect: Resources that promote your career growthLeaders that support flexible work schedulesPrograms to help you build your therapeutic knowledgeDynamic work environments that expose you to new experiencesHome-office, company car, and more Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™. Please apply with your English CV. #CRASDAJD #CRA #SCRA #SeniorCRA #iqvia #fspcares 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 171.900,00 zł - 375.700,00 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 our team as a Site Enrollment and Engagement Lead and play a pivotal role in advancing clinical research. This role collaborates with research staff and stakeholders to drive trial recruitment and deliver study-specific training. Acting as a strategic partner, you will optimize site experience and performance while fostering strong relationships and sharing medical and scientific information with healthcare providers and caregivers. Key Responsibilities Develop study-specific action plans with research sites to accelerate recruitment and support procedural training. Educate healthcare professionals and their staff on study protocols related to clinical trials. Partner with referral networks to identify potential trial participants. Maintain and analyze customer records to tailor strategies for pre-screening, screening, and enrollment. Complete internal reporting and organize group events to optimize program delivery. Address and manage objections effectively. Stay current with technical knowledge in relevant therapeutic areas. Qualifications Bachelor's Degree (BA/BS) in Health Sciences or related field, or equivalent academic/professional qualifications Clinical research experience at the site level required Nurse or other healthcare professional preferred CRA experience preferred High flexibility to travel (including internationally if needed). Clinical competence in the therapeutic area. Excellent interpersonal and communication skills. Strong written and verbal communication skills. Ability to work independently and coordinate across multiple functions. Solutions-oriented approach and positive attitude. Strong customer service orientation and collaborative mindset. Demonstrates empathy and cultural awareness. Upholds values of IQVIA. Why Join Us?At IQVIA, we are committed to improving patient outcomes through innovation and collaboration. As a Site Enrollment and Engagement Lead you will make a meaningful impact on clinical research and contribute to advancing healthcare globally. 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 102 800,00 zł - 190 900,00 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.

We are seeking Lab Operations Associate 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 Lab Operations Associate supports the routine receipt, inspection, and processing of clinical specimens to help maintain efficient laboratory operations. This role also assists with shipment handling, inventory support, workstation organization, and adherence to safety and quality procedures. What You'll Be Doing:Receive consignments and shipments and assist with specimen intake activitiesOpen shipments, review patient information forms, and escalate missing, incorrect, or damaged materials to senior staffVerify that specimens have been fully removed from kit packaging through secondary checksDispose of or recycle kit shipping supplies in accordance with site proceduresSupport equipment upkeep, inventory activities, and general workstation clean-upRespond to after-hour alarms and other job-critical operational needs as requiredPerform administrative duties and maintain an organized work area in line with management expectations What We Are Looking For:High School Diploma or equivalent requiredBasic computer skillsAbility to maintain effective reporting procedures and control workflowThe Knowledge, Skills and Abilities Needed for This Role:Ability to establish and maintain effective working relationships with coworkers, managers and clientsStrong attention to detail when handling clinical specimens, shipment materials, and documentationAbility to follow company procedures, safety requirements, and applicable regulatory guidelinesAbility to stay organized and manage routine tasks in a fast-paced laboratory environmentAbility 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 $25,300.00 - $52,700.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job OverviewManage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team to provide high quality data management products that meet customer needs. Provide leadership to the team in the areas of project planning, execution, and close-out; Overview of financial management for data management activities; communications; and milestone deliverables. Perform role of Data Team Lead (DTL).  Essential Functions• Gather Study Set up requirements through discussion and communication with relevant stakeholders.• With Minimal guidance - support, overview of validation of new Device integrations.• Oversight & Perform regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor.• Ensure that all the deliverables are of expected quality standards and meet customer expectations.• With guidance, ensure service and quality meet agreed upon timelines and deliverables in contract/Scope of Work (SOW).• Support Training of New joiners.• Lead internal study meetings and internal/ sponsor audits and participate in Study Kick off meetings and other sponsor meetings.• Tracks and manages the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended as required.• With Guidance manage & oversight the implementation of new technology / database revisions.• Work closely with the programming team for process innovation and automation.• Be compliant to trainings and eSOP reading.• Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions.• Communication with Line Manager, and other team members across functions should be collaborative.• Perform other duties as directed by Line Manager. Qualifications• Bachelor's Degree In health, clinical, biological or mathematical sciences, or related field with proven experience in Data Management Req• 3 -4 years direct Data Management experience, including a minimum of 1 year as a CDM project lead. Pref• English Fluency Spoken and English Advanced• Advanced computer applications like Microsoft excel, word, Inbox etc Advanced• Should have Advanced understanding of Drug development lifecycle and Overall Clinical research process Advanced IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Overview1. Ensures compliance with established internal control procedures by examining records, reports, operating practices and documental2. Responsible for auditing event compliance which includes validation of expenses such as Travel, Food, Audio Visual, Speaker payment and other Fees for policy compliance3. Facilitates cross-training and trains new hires on client specific protocols, SOP and audit parameters4. Facilitates internal calibration to ensure all team members are aligned on client SOP and procedures5. Maintains and updates audit and process documents6. Provides audit related and ADHOC reports7. Recommends process improvements8. Performs internal Quality Audit of output of Sub team members9. Conducts coaching and mentoring of Sub team members10. Provides insights during stakeholder meetingsEssential Functions1. Audits compliance of pharmaceutical events using regulatory/client specific policies and acts as the final checker/processor of the financial close and review task2. Monitor and maintains audit guidelines updated to client policies and procedure3. Returns/clarify identified non-compliant submissions from financial close & review and provide coaching/feedback when necessary4. Facilitates certification activities and calibration with FC & R Planners to ensure compliance on submitted transactions5. Responsible to prepare routine reports and analysis that are high quality, accurate and timely. Acts as a key contact for any concerns/relative issues for the assigned clientsQualifications1. Graduate of any finance, business-related course and/or with at least 1 to 2 years experience in the following:a. Compliance and Quality Auditor (Finance Account or Shared Services format)b. Travel and Expense Specialistc. Accounts Payable Specialist 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.

Senior Software Developer (m/w/d) full remote Singen, Deutschland Home-office/Remote IQVIA ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Als Geschäftsbereich EPIS – Emergency & Practice Information System – mit Sitz in Singen entwickeln wir ein modernes, webbasiertes Praxisverwaltungssystem, das den Arbeitsalltag in medizinischen Einrichtungen effizienter und sicherer macht. Unser Kernprodukt umfasst neben der Webanwendung mehrere ergänzende webbasierte und native Anwendungen und bietet eine Vielzahl modularer Komponenten. Unser Fokus liegt auf Lösungen, die den hohen Anforderungen des Gesundheitswesens gerecht werden und gleichzeitig Raum für individuelle Anpassungen bieten. So schaffen wir ein System, das nicht nur zuverlässig und regelkonform ist, sondern auch flexibel auf die Bedürfnisse unserer Kunden eingeht. Deine Aufgaben Konzeption, Entwicklung und Pflege unserer Webanwendungen sowie nativer Verwaltungsanwendungen auf Basis von C#, .NET, Blazor, JavaScript und SQL Server Mitarbeit bei der technischen Konzeption sowie Weiterentwicklung bestehender und neuer Komponenten im Frontend und Backend Design und Implementierung von REST-Schnittstellen sowie Integration externer Systeme und Dienste Umsetzung funktionaler und technischer Anforderungen in enger Zusammenarbeit mit Architektur, Product Ownern und Fachbereichen Übernahme ausgewählter DevOps-Aufgaben im Bereich Build-, Release- und Deployment-Management sowie Weiterentwicklung unserer CI/CD-Pipelines Steuerung und technische Umsetzung regulatorischer und fachlicher Anforderungen im Gesundheitswesen, insbesondere im Rahmen von Zertifizierungsverfahren der KBV, Gematik und weiterer relevanter Institutionen Sicherstellung von Codequalität und Softwarestandards durch Code Reviews, automatisierte Tests und Mentoring von Junior-Entwicklern Nutzung moderner Werkzeuge wie Azure DevOps, Git und automatisierter Build- und Deployment-Prozesse Mitarbeit bei der kontinuierlichen Verbesserung von Entwicklungsprozessen, Werkzeugen und technischen Standards Enge Zusammenarbeit mit Product Ownern, Fachbereichen und weiteren Stakeholdern zur optimalen Umsetzung von Kunden- und Marktanforderungen Dein Profil Abgeschlossenes Studium der Informatik oder vergleichbare Qualifikation Mehrjährige Berufserfahrung in der Full-Stack-Entwicklung mit modernen .NET-Technologien Sehr gute Kenntnisse in C#, JavaScript, Blazor und relationalen Datenbanken (SQL Server) Erfahrung in der Entwicklung und Integration von REST-Schnittstellen Erfahrung mit modernen Entwicklungswerkzeugen und -methoden, insbesondere Git, Azure DevOps sowie CI/CD-Prozessen Interesse an der Weiterentwicklung von CI/CD-, Build- und Deployment-Prozessen Erfahrung im Umgang mit regulatorischen Anforderungen sowie idealerweise mit Zertifizierungsverfahren im Gesundheitswesen Wünschenswert sind Kenntnisse moderner Authentifizierungs- und Autorisierungstechnologien (z. B. OAuth2, OpenID Connect, Duende IdentityServer, Keycloak oder vergleichbare Lösungen) Idealerweise Erfahrung im Gesundheitswesen, insbesondere im Umfeld von KBV-, Gematik-, TI- oder anderen eHealth-Lösungen Ausgeprägte Team- und Kommunikationsfähigkeit, hohe Eigeninitiative sowie eine strukturierte und lösungsorientierte Arbeitsweise Sehr gute Deutsch- und gute Englischkenntnisse Werde Teil unseres Teams und arbeite im spannenden und innovativen Umfeld des Gesundheitswesens.  Worauf Du Dich freuen kannst: Willkommen in unserem Team mit individuellen Entwicklungsmöglichkeiten Ein sehr gutes Arbeitsumfeld mit wertschätzendem Umgang, hoher Kollegialität und offener Zusammenarbeit im Team Strukturierte Einarbeitung und Wissenstransfer Vielseitige Tätigkeit in einem dynamischen IT-Unternehmen mit Weiterbildungsmöglichkeiten Flexible Arbeitszeitmodelle und Möglichkeit einer Tätigkeit im Homeoffice (100%), Telearbeit oder am Firmenstandort Neue offene Büroflächen in super Lage in Singen am Bodensee mit vielen Freizeitmöglichkeiten Rabatte über IQVIA Corporate Benefits IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job Summary The Director, Regulatory Affairs-JAPAC MedTech serves as a strategic regulatory leader and trusted advisor to medical technology clients across Japan and the Asia-Pacific region. This client-facing role is responsible for developing and leading regulatory strategies that support product development, market access, and commercialization for medical devices, diagnostics, digital health technologies, software as a medical device (SaMD), and combination products. The Director will lead complex regional and global regulatory programs, provide expert regulatory consulting, build strong client relationships, and support business growth initiatives. This individual will collaborate with cross-functional teams and senior stakeholders to deliver high-quality regulatory solutions that help clients successfully navigate evolving global regulatory environments. Job Responsibilities Provide strategic regulatory guidance and consulting to MedTech clients across Japan and the Asia-Pacific region.Develop and execute regulatory strategies for product registrations, market access, lifecycle management, and compliance initiatives.Lead complex regulatory programs, including multi-country submissions, global registration strategies, and U.S. FDA bridging activities.Serve as a trusted advisor to senior client stakeholders, providing regulatory leadership and risk-based recommendations.Direct large-scale regulatory projects, ensuring timely delivery, quality execution, effective resource management, and budget oversight.Lead interactions with regulatory authorities and support regulatory inspections, audits, and compliance activities.Partner with commercial and account teams to identify new business opportunities, support proposal development, and participate in client presentations and bid defenses.Drive operational excellence through continuous improvement of regulatory processes, tools, and delivery models.Mentor and develop regulatory professionals, fostering collaboration, knowledge sharing, and team growth.Represent IQVIA at industry conferences, professional forums, and client meetings through thought leadership and regulatory expertise.Job Qualifications Required Education Bachelor's degree in Life Sciences, Pharmacy, Biomedical Engineering, Regulatory Affairs, Engineering, or a related discipline.Advanced degree (Master's, MBA, or equivalent) and/or RAC certification preferred.Required Experience 12+ years of Regulatory Affairs experience within the medical device, diagnostics, digital health, biotechnology, or broader healthcare industry.Significant experience supporting Japan regulatory activities and broader Asia-Pacific regulatory programs.Proven success leading complex regulatory projects, global submissions, and multi-country regulatory strategies.Experience working directly with health authorities and senior client stakeholders.Consulting or professional services experience strongly preferred.Knowledge, Skills, and Abilities Deep knowledge of global medical device and diagnostic regulatory requirements, including PMDA, FDA, TGA, NMPA, MFDS, HSA, and other regional regulatory frameworks.Strong understanding of quality systems, clinical evidence requirements, risk management, and post-market regulatory obligations.Demonstrated expertise in regulatory strategy development for innovative technologies, including digital health and software-based medical products.Excellent leadership, stakeholder management, communication, presentation, and influencing skills.Strong business acumen with the ability to identify opportunities, solve complex regulatory challenges, and drive client success.Ability to lead cross-functional and geographically dispersed teams in a fast-paced, global environment.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Essential Functions Responsible for performing and documenting analytical procedures in accordance with SOPs and regulatory guidelines.Performs routine data analysis to determine if an analytical procedure is proceeding according to expectations and that the results are within acceptable tolerances.Identifies and documents potential performance errors or otherwise unusual results and escalates to senior lab personnel.Prepares data analysis results for upload to LIMS system under the guidance of senior level staff.Assists in quality investigations, deviations, and resolution.Prepares buffers and solutions for analysis, as required.Assists in the review and update of laboratory procedures and techniques.Guides entry level staff on routine procedures and supports on-boarding of new staff.Performs and document calibration and maintenance of laboratory equipment as assigned.Performs and documents hands on training for other lab personnel in areas of proven competency as assigned.Assists in the review and development of laboratory procedures and techniques.Assists in the implementation of procedural changes as assigned.Notifies inventory staff of supply shortages.May represent lab team on cross functional projects.Responsible for clear, accurate, and timely communications with cross functional stakeholders.Participates in continuing education through self-study, attending training sessions and lectures and meetings.Supports safety, quality, and 6S requirements and initiatives.Complies with company's procedures and applicable regulatory requirements.Qualifications Bachelor's Degree or equivalent combination of education and experience (Some CAP/CLIA lab locations may require a BSc in in a chemical, physical, biological or clinical laboratory science, medical laboratory technology or cytotechnology.)Comfortable with rotating between afternoon and night shiftsMin 6 months experience in a regulated laboratory environment.Requires basic knowledge of assigned technical area, systems and procedures obtained through prior work experience.Demonstrates understanding of functional area and responsibilities.Working knowledge of any applicable regulatory standards within area of responsibility, such as Good Laboratory Practices (GLP).Proficiency with relevant laboratory techniques.Knowledge of laboratory safety and infection control procedures and practices including standard precautions and hazardous chemical handling.Experience working with automation or specialized laboratory equipment.Proficiency with routine and some non-routine laboratory calculations regarding batches and specimens including averages, means, standard deviations, and various quality control metrics.Capable of handling multiple tasks simultaneously.Strong attention to detail and accuracy.Ability to effectively collaborate with internal stakeholders.Applicable certificates and/or other regulatory bodies by country, state, and/or other regulatory bodiesIQVIA 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 responsibilities:1. Participate in and be responsible for industry information collection and collation, desk research, and research report/literature translation;2. Assist consultants to conduct interview outline design for industry experts, write interview summaries and dig deep insight information;3. Use Excel or other data analysis software to collect, clean and analyze data;4. Assist consultants to complete the report writing and PPT production delivered to the client.5. Flexibility to support team members with other work assignments. Job Requirements:1. Undergraduate and graduate students in medicine, pharmacy, biology and other related majors, with previous experience in consulting firms, brokerage firms or other related internships preferred;2. Fluent in English, listening, reading and writing;3. Proficient in the use of office software, especially excel;4. Serious and careful, hard-working, able to accept overtime.5. Start as soon as possible, at least 3 days a week for 3 months or more. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewUnder moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements  at the regional, or country level. Prepares and manages site documentation; reviews and negotiates site  documents and contracts with sites and sponsors; maintains, reviews, and reports on site performance metrics; serves as the primary point of contact for investigative sites; tracks completion of appropriate documents for sites; ensures contracts are fully executed; and establishes project timelines.  With moderate oversight and supervision, perform tasks at a country/region level associated with site activation activities in accordance with  applicable local and/or internationalregulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions• With moderate oversight and supervision, werve a Single Point of Contact (SPOC) to perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the  Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.• Prepare site documents, reviewing for completeness and accuracy.• Inform team members of completion of regulatory contractual. and other documents for individual sites.• Distribute completed documents to sites and internal project team members.• Update and maintain internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.• Review, track and follow up the progress, the approval and execution of required documents such as questionaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents. Requires advanced knowledge within a specific discipline typically gained through extensive work experience and/or education. Qualifications• BA/BS degree in Life Sciences, Nursing or related scientific field (or equivalent experience).• Required: At least 1-2 years of Regulatory Affairs experience from global/local CRO. • Proficient in English language (spoken and written). IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

This is a talent pool for people with disabilities. If you do not belong to this group and wish to apply, you can apply for other vacancies within IQVIA jobs. Job Overview IQVIA is committed to fostering an inclusive workplace where diversity drives innovation. This opportunity is exclusively intended for People with Disabilities (PwD). Location: São Paulo, BrazilWork Model: HybridEmployment Type: Full-time As a Talent Acquisition Assistant, you will support recruitment activities across Latin America, partnering with recruiters and stakeholders to ensure a positive candidate experience and efficient hiring processes. The role combines recruitment coordination, talent market insights, sourcing support, and administrative activities. Key Responsibilities Support recruitment operations and maintain accurate candidate data and reports.Gather talent market insights and feedback from new hires across LATAM, with a focus on Brazil.Coordinate interviews and manage scheduling between candidates and hiring teams.Support candidate sourcing initiatives through LinkedIn and other recruiting channels.Assist with job posting, employer branding, and talent attraction activities.Provide general administrative support to the Talent Acquisition team.Qualifications Bachelor's degree in Human Resources, Psychology, Business Administration, Communications, or a related field.Previous experience in recruitment, talent acquisition coordination, administration, or customer-facing support roles is a plus.Strong organizational skills and attention to detail.Experience working with MS Office, ATS platforms or LinkedIn is preferred.Intermediate level of English and/or Spanish.Strong communication and teamwork skills.Inclusion Statement IQVIA is an equal opportunity employer and is committed to creating an inclusive environment for all employees. This position is exclusively intended for People with Disabilities (PwD). If you require accommodations during the recruitment process, please indicate your needs when applying. All information will be handled confidentially and in accordance with applicable regulations 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.

Acreditamos que a diversidade impulsiona a inovação, fortalece nossos times e contribui para a construção de um ambiente mais colaborativo, inclusivo e acolhedor para todos. Por isso, estamos formando nosso Banco de Talentos para Pessoas com Deficiência (PcD) e buscamos profissionais que desejem construir uma trajetória de desenvolvimento, crescimento e impacto conosco. Se você procura um ambiente que valoriza diferentes experiências, perspectivas e habilidades, queremos conhecer você! Ao se cadastrar em nosso Banco de Talentos na IQVIA, seu perfil poderá ser considerado para oportunidades atuais e futuras em diversas áreas da companhia, incluindo: Recursos Humanos (HR)Finanças (Finance)ClinicalSales & Client ServicesTecnologia (Technology)Outras áreas corporativas e de negóciosCadastre seu currículo e venha fazer parte da nossa comunidade de talentos. Responsabilidades:As atividades poderão variar de acordo com a área de atuação e o nível da posição, podendo incluir: Apoio a projetos, processos e rotinas da área;Organização, atualização e controle de informações, documentos e sistemas;Elaboração de relatórios, análises, apresentações e materiais de suporte;Atendimento e suporte a clientes internos e/ou externos;Participação em iniciativas de melhoria contínua e inovação;Colaboração com equipes multidisciplinares para alcance de resultados e metas;Suporte às atividades operacionais, administrativas, técnicas ou estratégicas da área.Requisitos:Ser uma Pessoa com Deficiência (PcD);Possuir laudo médico atualizado que comprove a condição de Pessoa com Deficiência (PcD);Ensino médio completo ou ensino superior em andamento/concluído, de acordo com a oportunidade;Conhecimento básico ou intermediário do Pacote Office;Boa comunicação, organização e capacidade de trabalhar em equipe;Interesse em aprender e se desenvolver profissionalmente;Disponibilidade para atuar em modelo híbrido na região da Chácara Santo Antônio, conforme necessidade da posição e da área.Diferenciais:Experiência prévia em áreas corporativas, comerciais, tecnológicas, clínicas ou de atendimento;Conhecimento em ferramentas e sistemas relacionados à sua área de atuação;Formação técnica ou superior em áreas correlatas;Conhecimento de inglês e/ou espanhol, que poderá ser utilizado em determinadas áreas, projetos e interações da empresa.A IQVIA está empenhada em adotar um ambiente de trabalho diverso e inclusivo. Nosso objetivo é atrair e reter as melhores pessoas, independentemente de gênero, raça, estado civil, origem étnica, nacionalidade, idade, deficiência, orientação sexual, identidade de gênero ou qualquer outra característica. Junte-se a nós! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Clinical Trial Manager – Sponsor Dedicated. Clinical Project Management services provide management of a clinical trial (s) in a local level. Services/deliverables include operational oversight of assigned project(s) at the local level for end-to-end project management from start-up through to closeout activities. Tasks & Responsibilities: • Services rendered will adhere to applicable Sponsor SOPs, WIs, policies, codes of Good Clinical Practice (GCP), local regulatory requirements. • Prepares or contributes to high level budget estimate in response to Request for Service’s followed by detailed budget proposal. Ensures overall contract management, including review and approval of external service provider (ESP) contracts, change orders and ensures services are delivered per contract. • Act as primary company contact for assigned trial at the country level and ensures local/country team is tracking project progress against planned timelines and monitors patient recruitment rate to ensure that target enrollment will be met across the allocated countries. This may require development of local trial specific procedures and tools, recruitment planning, contingency and risk management, and budget forecasting. • Drive study compliance by maintaining and updating trial management systems, using study tools and management reports available to analyze trial progress. Participates in preparation for and conduct of Health Authority (HA) inspections and internal Quality Assurance audits. Escalates corrective and preventive actions (CAPA) to GTL MAO and CPL when the trial deviates from plans and communicates study progress and issues to study management teams and business partners. • Contributes to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target. • Contributes to patient understanding of protocol and patient safety by contributing to the review of country specific informed consent in accordance with procedural document/templates. This includes reviewing and managing site specific informed consent forms in accordance with SOPs, other procedural documents and applicable regulations. Essentials Requirements: • BA/BS degree. • Degree in a health or science related field. • Minimum of 2 years of local/regional trial management experience in the pharmaceutical industry or CRO and previous experience as Clinical Research Associate. • Specific therapeutic area experience may be required depending on the position. • Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures. • Strong IT skills in appropriate software and company systems. Willingness to travel with occasional overnight stay away from home according to business needs. • Excellent decision-making and string financial management skills. • Proficient in speaking and writing the country language and English. Good written and oral communication skills as appropriate. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Resumen del puestoBajo supervisión y seguimiento cercano, esta posición es responsable de reclutar farmacias y médicos, así como administrar programas de recolección de datos y compensación para participantes.Responsabilidades principalesRealizar llamadas a farmacias utilizando una estrategia comercial predefinida y desarrollar habilidades para contactar también a médicos.Promover la participación de farmacias y médicos en paneles de investigación de mercado continuos (sindicados), cumpliendo los estándares de reclutamiento, reporte y diseño de muestra.Realizar llamadas de seguimiento para maximizar la participación y la tasa de respuesta de los panelistas.Recibir y gestionar llamadas entrantes de los participantes, derivando consultas complejas al supervisor cuando corresponda.Preparar y enviar documentos físicos para la recolección de datos.Administrar estrategias de captura electrónica de datos con los participantes asignados.Capacitar, educar y motivar a médicos y farmacias para que cumplan con los lineamientos de los estudios.Gestionar incentivos y compensaciones de los participantes, investigando y resolviendo incidencias para asegurar pagos oportunos.Colaborar con equipos internos, como el de codificación, para resolver problemas relacionados con la calidad de los datos.Brindar apoyo en actividades de reclutamiento y entrevistas para proyectos o estudios especiales.Mantener actualizada la información de los proveedores y participantes cuando sea necesario.RequisitosEstudios secundarios completos.Manejo de herramientas Microsoft Office, especialmente Excel, Word, Access y Outlook.Buenas habilidades de comunicación verbal y persuasión.Capacidad analítica para interpretar información y resolver problemas.Idioma portugués avanzado.Perfil idealBuscamos una persona con experiencia realizando llamadas outbound, reclutando profesionales de la salud, gestionando relaciones con médicos o farmacias y haciendo seguimiento continuo para asegurar su participación en estudios o paneles de investigación. Debe sentirse cómoda trabajando por objetivos, tener habilidades de persuasión y una fuerte orientación al servicio y al detalle.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 OverviewThis individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, ability to prioritize, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills. Essential Functions• Develop strong working relationships and maintain effective communication with study team members• Develop strong working relationships with the investigators and office staff to build a foundation of trust and respect between the clinic and the research office• Assists with the screening, recruiting and enrollment of research subjects• Perform patient/research participant scheduling• Collect patient/research participant history• Data entry and management• Coordinate follow up care and laboratory procedures• Adhere to an IRB approved protocol• Assist in the informed consent process of research subjects• Support the safety of research subjects• Coordinate protocol related research procedures, study visits, and follow up care• Comply with company and Sponsor policies, standard operating procedures (SOPs) and guidelines• Schedule subject visits and procedures Qualifications• High School Diploma or equivalent  Req• Bachelor's Degree  Pref 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 $35,800.00 - $89,400.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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. The Instrument Development and Thought Leadership Segment Instrument Development: This team is responsible for the development of new clinical outcome instruments, expansion and enhancement of existing instruments, with a focus on specific priority therapeutic area. Collaborative &Y. Advisory: Given the team’s expertise in instrument development and client consulting and delivery, team members support where appropriate client consulting engagement with the PACT team and collaborate with therapeutics centers of excellence.  Thought leadership is the final area of focus: This includes white papers, manuscripts/publications, podium presentations; posters and books.  Coordination with the PACT team, clients, industry thought leaders, regulators, patient advocacy groups and other stakeholders is a critical component of our thought leadership. The role The Head of Patient and Instrument Science and Thought Leadership leads the strategic, scientific and regulatory development of Clinical Outcomes Assessments (COAs) and Composite Measures. COA’s include: Patient-Centered Research patient-reported outcomes (PROs), observer-reported outcomes (ObsROs), and clinician-reported outcomes (ClinROs).  These instruments are used by BioPharmaceutical and Medical Device organization in clinical trials and real-world studies and by Health Care Physicians in day-today clinical practice. This individual is responsible for ensuring that the patient perspective is rigorously measured and incorporated into drug development, measurement endpoint strategy, regulatory submissions, and commercialization using behavioral and measurement science. Responsibilities: Strategic Leadership: Define instrument development strategies across therapeutic areas, ensuring alignment with Instrument Licensing & Services, R&DS Therapeutic Area Priorities and R&DS goals, FDA/EMA guidance on patient-focused drug development (PFDD), and HTA requirements.Scientific Excellence: Lead the development, validation, and implementation of new and existing COA instruments, including psychometric evaluation, qualitative research, and endpoint definition. Support the Scientific & Strategic Research Consulting team in their client facing COA endpoint strategy projects as needed.Regulatory Engagement: Lead interactions with regulatory bodies (FDA, EMA) regarding newly developed COAs designed to replace older declining in relevance COAs.Methodological Expertise: Direct the use of advanced methodologies, with a heavy focus on Domains of Health, including Digital Measurement Plans, eCOA (electronic COA) strategies, and Patient Experience Data (PED) analytics.Cross-functional Collaboration: Partner with Instrument Licensing & Services (IQVIA Quality Metric), Strategic & Scientific Research, R&DS Design & Delivery Innovation including the TSSU/Therapeutic Area COE, clinical operations, biometrics, regulatory, and commercial teams build, expand and enhance COA utility in measuring meaningful change in health.Team Leadership: Mentor and build a team of experienced and burgeoning scientists, guiding them in COA methodologies and scientific best practices. Participate in acquisition science and staff integration as relates to COA assets and scientific SME’s.External Representation: Act as a recognized expert in the field, representing the company at scientific conferences (e.g., ISPOR, ISOQOL, CPATH, etc) and in industry consortia. Required Qualifications & Skills – our ideal candidate will have: Education: Advanced degree (PhD, Master’s, or equivalent) in Psychology, Behavioral measurement, Health Services Research, Epidemiology, Pharmacy, Public Health, or a related discipline.Experience: 10+ years of professional experience in COA/outcomes research within pharmaceutical, CRO, or consultancy settings, with a strong track record of publications.Technical Knowledge: Deep understanding of COA methodology, psychometrics, FDA/EMA regulatory guidelines on patient-focused drug development, and qualitative research methods.Communication: Excellent scientific writing and verbal skills, with the ability to communicate complex data to regulatory bodies and internal senior leadership.Influencing & Relationship Development: Proven influencing skills at the senior management level, have the presence and credibility to engage and influence senior leaders across multi-geographies and functions. Demonstrated success building effective relationships with a broad spectrum of global stakeholders (e.g., senior leaders, business and technical teams, GTM, and customers)Leadership: Proven experience in managing high-performing teams, building talent, and influencing cross-functional stakeholders. Promotes information sharing and demonstrates flexibility to work in a fast paced, dynamic environment and effectively manage change.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.

Job OverviewProvides high quality, on-time input to client projects in the life sciences field. Assignments typically require analysis and problem solving within an established framework. Essential Functions• Under direct supervision, assists with the review and analysis of client requirements or problems and assists in the development of client solutions.• Assists in the development of detailed documentation and specifications.• Under close supervision, performs quantitative or qualitative analyzes to assist in the identification of client issues and the development of client specific solutions.• Assists in the design and structure of presentations that are appropriate to the characteristics or needs of the audience.• Proactively develops a basic knowledge of consulting methodologies and the life sciences market through the delivery of consulting engagements and participation in formal and informal learning opportunities.• Engagement based responsibilities are assigned and closely managed by Consultants, Senior Consultants, Engagement Managers or Principals. Qualifications• Bachelor's Degree  Req• 1-3 years of related experience Req• Works willingly and effectively with others in and across the organization to accomplish team goals.• Knowledge and understanding of the fundamental processes of business, their interaction, and the impact of external/internal influences on decision making, growth and decline.• Knowledge of consulting methods, tools and techniques, related to one’s functional area.• Knowledge of current events and developments within an industry and major competitors.• Knowledge and understanding of the marketplace. Knowledge of professional/trade associations, key people and companies.• Effective time management skills. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewProvides high quality, on-time input to client projects in the life sciences field. Assignments typically require analysis and problem solving within an established framework. Essential Functions• Under direct supervision, assists with the review and analysis of client requirements or problems and assists in the development of client solutions.• Assists in the development of detailed documentation and specifications.• Under close supervision, performs quantitative or qualitative analyzes to assist in the identification of client issues and the development of client specific solutions.• Assists in the design and structure of presentations that are appropriate to the characteristics or needs of the audience.• Proactively develops a basic knowledge of consulting methodologies and the life sciences market through the delivery of consulting engagements and participation in formal and informal learning opportunities.• Engagement based responsibilities are assigned and closely managed by Consultants, Senior Consultants, Engagement Managers or Principals. Qualifications• Bachelor's Degree  Req• 1-3 years of related experience Req• Works willingly and effectively with others in and across the organization to accomplish team goals.• Knowledge and understanding of the fundamental processes of business, their interaction, and the impact of external/internal influences on decision making, growth and decline.• Knowledge of consulting methods, tools and techniques, related to one’s functional area.• Knowledge of current events and developments within an industry and major competitors.• Knowledge and understanding of the marketplace. Knowledge of professional/trade associations, key people and companies.• Effective time management skills. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job OverviewProvides high quality, on-time input to client projects in the life sciences field. Assignments typically require analysis and problem solving within an established framework. Essential Functions• Under direct supervision, assists with the review and analysis of client requirements or problems and assists in the development of client solutions.• Assists in the development of detailed documentation and specifications.• Under close supervision, performs quantitative or qualitative analyzes to assist in the identification of client issues and the development of client specific solutions.• Assists in the design and structure of presentations that are appropriate to the characteristics or needs of the audience.• Proactively develops a basic knowledge of consulting methodologies and the life sciences market through the delivery of consulting engagements and participation in formal and informal learning opportunities.• Engagement based responsibilities are assigned and closely managed by Consultants, Senior Consultants, Engagement Managers or Principals. Qualifications• Bachelor's Degree  Req• 1-3 years of related experience Req• Works willingly and effectively with others in and across the organization to accomplish team goals.• Knowledge and understanding of the fundamental processes of business, their interaction, and the impact of external/internal influences on decision making, growth and decline.• Knowledge of consulting methods, tools and techniques, related to one’s functional area.• Knowledge of current events and developments within an industry and major competitors.• Knowledge and understanding of the marketplace. Knowledge of professional/trade associations, key people and companies.• Effective time management skills. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

External Job DescriptionJoin 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. The Instrument Development and Thought Leadership Segment Instrument Development: This team is responsible for the development of new clinical outcome instruments, expansion and enhancement of existing instruments, with a focus on specific priority therapeutic area. Collaborative &Y. Advisory: Given the team’s expertise in instrument development and client consulting and delivery, team members support where appropriate client consulting engagement with the PACT team and collaborate with therapeutics centers of excellence.  Thought leadership is the final area of focus: This includes white papers, manuscripts/publications, podium presentations; posters and books.  Coordination with the PACT team, clients, industry thought leaders, regulators, patient advocacy groups and other stakeholders is a critical component of our thought leadership. The role The Head of Patient and Instrument Science and Thought Leadership leads the strategic, scientific and regulatory development of Clinical Outcomes Assessments (COAs) and Composite Measures. COA’s include: Patient-Centered Research patient-reported outcomes (PROs), observer-reported outcomes (ObsROs), and clinician-reported outcomes (ClinROs).  These instruments are used by BioPharmaceutical and Medical Device organization in clinical trials and real-world studies and by Health Care Physicians in day-today clinical practice. This individual is responsible for ensuring that the patient perspective is rigorously measured and incorporated into drug development, measurement endpoint strategy, regulatory submissions, and commercialization using behavioral and measurement science. Responsibilities: Strategic Leadership: Define instrument development strategies across therapeutic areas, ensuring alignment with Instrument Licensing & Services, R&DS Therapeutic Area Priorities and R&DS goals, FDA/EMA guidance on patient-focused drug development (PFDD), and HTA requirements. Scientific Excellence: Lead the development, validation, and implementation of new and existing COA instruments, including psychometric evaluation, qualitative research, and endpoint definition. Support the Scientific & Strategic Research Consulting team in their client facing COA endpoint strategy projects as needed. Regulatory Engagement: Lead interactions with regulatory bodies (FDA, EMA) regarding newly developed COAs designed to replace older declining in relevance COAs. Methodological Expertise: Direct the use of advanced methodologies, with a heavy focus on Domains of Health, including Digital Measurement Plans, eCOA (electronic COA) strategies, and Patient Experience Data (PED) analytics. Cross-functional Collaboration: Partner with Instrument Licensing & Services (IQVIA Quality Metric), Strategic & Scientific Research, R&DS Design & Delivery Innovation including the TSSU/Therapeutic Area COE, clinical operations, biometrics, regulatory, and commercial teams build, expand and enhance COA utility in measuring meaningful change in health. Team Leadership: Mentor and build a team of experienced and burgeoning scientists, guiding them in COA methodologies and scientific best practices. Participate in acquisition science and staff integration as relates to COA assets and scientific SME’s. External Representation: Act as a recognized expert in the field, representing the company at scientific conferences (e.g., ISPOR, ISOQOL, CPATH, etc) and in industry consortia.  Required Qualifications & Skills – our ideal candidate will have: Education: Advanced degree (PhD, Master’s, or equivalent) in Psychology, Behavioral measurement, Health Services Research, Epidemiology, Pharmacy, Public Health, or a related discipline. Experience: 10+ years of professional experience in COA/outcomes research within pharmaceutical, CRO, or consultancy settings, with a strong track record of publications. Technical Knowledge: Deep understanding of COA methodology, psychometrics, FDA/EMA regulatory guidelines on patient-focused drug development, and qualitative research methods. Communication: Excellent scientific writing and verbal skills, with the ability to communicate complex data to regulatory bodies and internal senior leadership. Influencing & Relationship Development: Proven influencing skills at the senior management level, have the presence and credibility to engage and influence senior leaders across multi-geographies and functions. Demonstrated success building effective relationships with a broad spectrum of global stakeholders (e.g., senior leaders, business and technical teams, GTM, and customers) Leadership: Proven experience in managing high-performing teams, building talent, and influencing cross-functional stakeholders. Promotes information sharing and demonstrates flexibility to work in a fast paced, dynamic environment and effectively manage change. 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™. PLEASE SUBMIT YOUR CV IN ENGLISH! 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.

Registered Dietician – New YorkLocation: Remote in United States Job Type: Per Diem About the OpportunityAre you a Registered Dietitian seeking a flexible and meaningful role in clinical research? IQVIA, a global leader in advancing healthcare and clinical research, is seeking experienced Registered Dietitians to support patients participating in clinical trials. This remote role focuses on delivering high‑quality nutrition assessments and counseling, particularly for individuals living with rare and complex conditions. This position is ideal for clinicians who want to leverage their expertise in a telehealth environment, contribute to innovative research, and earn supplemental income while maintaining flexibility. Key ResponsibilitiesAs a Remote Registered Dietitian, you will: Conduct nutritional assessments via telehealth and develop individualized dietetic care plans for patients with varying disease classifications Provide ongoing dietary counseling and education to patients and their families Deliver nutrition services only to patients in states where you are licensed to practice Support patients enrolled in clinical research studies by monitoring nutritional progress and adherence Maintain accurate, timely, and confidential clinical documentation Participate in virtual team meetings, training sessions, and study‑related activities QualificationsCredentialed Registered Dietitian (CDR) with current national registration Active, unrestricted state licensure (except CA, MI, NJ, AZ, VA, and CO) Minimum 1 year of experience providing nutrition planning and patient coaching Minimum 1 year of experience delivering care remotely via telehealth Strong communication and interpersonal skills Experience working with patients with obesity, with or without diabetes (preferred) Experience managing patients on GLP‑1 therapies (preferred) Spanish‑English bilingual proficiency preferred Why Join IQVIA?Flexible per diem schedule that fits your lifestyle Opportunity to gain exposure to clinical trials and research‑focused care Competitive supplemental income Be part of a global organization advancing innovation and patient outcomes Additional InformationThis position is not eligible for visa sponsorship. Ready to make a meaningful impact from anywhere?Apply today and help support patients while contributing to the future of healthcare research. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role is 45 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.