Acts as a key liaison between clinical teams, remote research clinicians, and investigator sites to execute decentralized trial visits. Responsibilities include coordinating visit logistics, managing system access, and ensuring compliance with GCP and HIPAA regulations.
IQVIA
229 Remote Job Openings at IQVIA
Lead the preparation and delivery of key aggregate safety reports and manage signal detection, validation, and evaluation activities. Collaborate with global cross-functional stakeholders to support safety strategies and regulatory authority inquiries.
The role involves receiving and documenting safety data from healthcare providers and patients via calls, chats, and emails. Responsibilities include creating Adverse Event and Product Quality Complaint reports and ensuring compliance with SOPs and regulations.
The specialist is responsible for processing and submitting safety reports to regulatory authorities while ensuring compliance with SOPs and guidelines. They will collaborate with functional teams and healthcare professionals to address project-related issues and maintain quality standards.
The specialist is responsible for processing and submitting safety reports to regulatory authorities while ensuring compliance with SOPs and guidelines. They will also liaise with functional teams and healthcare professionals to address project-related issues.
Responsible for generating study strategies and performing data mining and analysis to provide recommendations for clinical research opportunities. Collaborates with internal stakeholders to deliver accurate country, site, and enrollment strategies for bid defense meetings.
Perform centralized monitoring activities to evaluate the quality and integrity of clinical studies according to protocols and regulations. Manage triggers, perform subject-level data reviews, and collaborate with cross-functional teams to resolve data issues.
Associate Manager / Manager, Project Services - Laboratories (Remote - West Coast)
IQVIA
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Full Time
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14 hours ago
IQVIA
Manage all laboratory aspects of clinical trial projects from award through closeout, serving as the primary point of contact for sponsors. Lead planning, risk management, and cross-functional coordination to ensure high-quality execution of protocol requirements.
Associate Manager / Manager, Project Services - Laboratories (Remote - East Coast)
IQVIA
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Full Time
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14 hours ago
IQVIA
Manage all laboratory aspects of clinical trial projects from award through closeout, serving as the primary point of contact for sponsors. Lead planning, risk management, and cross-functional coordination to ensure high-quality execution of protocol requirements.
Coordinator / Senior Coordinator, Project Services - Laboratories (Remote - East Coast)
IQVIA
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Full Time
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14 hours ago
IQVIA
Manage laboratory-related aspects of clinical trial projects from startup through closeout. Partner with Project Managers and cross-functional teams to ensure high-quality execution and timely delivery of milestones.
Attaché de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
IQVIA
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Full Time
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2 days ago
IQVIA
The CRA II is responsible for monitoring Phase I-IV oncology clinical trials to ensure compliance with protocols and regulatory requirements. Key duties include conducting site visits, training personnel, and managing site activities from start-up to close-out.
Own the day-to-day execution and roadmap for Provider Solutions, translating product strategy into actionable requirements and scalable solutions. Partner with engineering, design, and commercial teams to deliver data-driven insights that improve healthcare organization performance.
The Vendor Startup Manager accelerates vendor service delivery during the startup phase of global clinical trials for Novartis. Key duties include managing protocol specifications, overseeing vendor onboarding, and executing User Acceptance Testing for IRT systems.
Oversee the delivery, governance, and optimization of IQVIA information assets for key MedTech accounts to ensure contractual compliance. Drive customer satisfaction, retention, and incremental growth through proactive issue resolution and cross-functional partnership.
Provide operational support and coordination for global clinical trials from planning through close-out. Manage trial documentation, systems, and logistics while ensuring compliance with SOPs and regulatory requirements.
Manage the end-to-end interview scheduling process by coordinating between candidates, hiring managers, and internal stakeholders. Support new-hire onboarding and contribute to the continuous improvement of Talent Acquisition delivery processes.
Lead a portfolio of complex patient support and hub service programs while managing large operational teams. Serve as the executive leader for client relationships, driving strategic account growth and ensuring contractual delivery commitments.
Gestionnaire associé(e), Services de projets en laboratoire (télétravail) / Associate Laboratory Project Services Manager (Remote)
IQVIA
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Full Time
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3 days ago
IQVIA
Manage all laboratory aspects of assigned clinical trial projects throughout the entire study lifecycle from startup to closeout. Act as the primary point of contact for customers while ensuring compliance with SOPs, policies, and good practices.
Lead the design and delivery of scalable AI solutions, including foundation models and knowledge graphs, for pharmaceutical and life sciences organizations. Act as a trusted advisor to stakeholders to translate scientific challenges into measurable business value and technical implementations.
Provide executive leadership for a portfolio of nursing and patient support programs, ensuring client satisfaction and operational performance. Lead large-scale healthcare service delivery operations and mentor directors while supporting business development and account growth.
Lead end-to-end data management for complex global clinical trials from setup to database lock. Act as the primary client contact while managing budgets, timelines, and mentoring junior staff.
The role involves developing scoring rules and algorithms for Clinical Outcome Assessments and providing statistical support for new measures and endpoints. Additionally, the position supports the COA Accelerator tool and contributes to scientific thought leadership through publications and conferences.
The Clinical Specialist ensures the integrity of clinical trial data by reviewing assessment scales and providing guidance to raters. Responsibilities include evaluating assessment quality, conducting live feedback sessions, and supporting rater performance through mock interviews.
The Clinical Specialist ensures the integrity of clinical trial data by reviewing assessment scales and providing guidance to raters on scoring techniques. Responsibilities include conducting live feedback sessions, performing mock interviews, and submitting accurate documentation.
The Clinical Specialist ensures the integrity of clinical trial data by reviewing assessment scales and providing guidance to raters on scoring techniques. Responsibilities include conducting live feedback sessions, performing mock interviews, and submitting accurate documentation.
The Clinical Specialist ensures the integrity of clinical trial data by reviewing assessment scales and providing guidance to raters on scoring techniques. Responsibilities include conducting live feedback sessions, performing mock interviews, and submitting accurate documentation.
The Clinical Specialist reviews psychiatric scales to ensure standardized assessment practices and data integrity. They provide guidance and feedback to raters through live discussions and functional assessments.
Administer standardized stroke scales and review assessments from other raters to ensure data quality and protocol compliance. Provide feedback to raters on scoring techniques and participate in calibration sessions to maintain certification.
The Clinical Specialist ensures the integrity of clinical trial data by reviewing assessment scales and providing guidance to raters. This includes conducting live interactions, performing mock interviews, and submitting accurate documentation.
The Clinical Specialist ensures the integrity of clinical trial data by reviewing assessment scales and providing guidance to raters. Responsibilities include conducting live feedback sessions, evaluating scoring techniques, and supporting rater performance through mock interviews.
The Clinical Specialist ensures the integrity of clinical trial data by reviewing assessment scales and providing guidance to raters. Responsibilities include evaluating assessment quality, conducting live feedback sessions, and supporting rater performance through mock interviews.
The Clinical Specialist ensures the integrity of clinical trial data by reviewing assessment scales and providing guidance to raters on scoring techniques. Responsibilities include conducting live feedback sessions, performing mock interviews, and submitting accurate documentation.
The specialist serves as the single point of contact for site activation activities, ensuring adherence to SOPs and regulatory guidelines. Responsibilities include preparing regulatory documents, tracking approvals, and maintaining internal project databases.
Provide education and resources to patients with acromegaly to help them manage their disease state and treatment compliance. Coordinate communication between patients and healthcare providers while documenting all interactions in a CRM system.
Spécialiste bilingue du soutien aux patients - télétravail / Bilingual Patient Support Specialist - REMOTE
IQVIA
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Full Time
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4 days ago
IQVIA
Acts as the primary contact in a call center to provide clinical support, program enrollment, and insurance navigation for patients and healthcare providers. Manages inbound calls, reports adverse events, and coordinates reimbursement services to ensure optimal patient outcomes.
Lead end-to-end data management for complex global clinical trials from setup to database lock. Serve as the primary client contact while managing timelines, budgets, and mentoring junior staff.
Define and govern enterprise-wide architecture strategies and roadmaps with a focus on clinical operations and trial management. Co-design target-state architectures and reference models to reduce technical debt and ensure scalability across the organization.
Spécialiste bilingue du soutien aux patients - télétravail / Bilingual Patient Support Specialist - REMOTE (Fixed-term)
IQVIA
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Full Time
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4 days ago
IQVIA
Acts as the primary contact in a call center to provide clinical support, program enrollment, and insurance navigation for patients and healthcare providers. Manages inbound calls, reports adverse events, and coordinates reimbursement services to ensure optimal patient outcomes.
Lead coding analyses and reimbursement assessments to develop market access strategies for medical technology clients. Manage client engagements, lead project teams, and provide strategic recommendations to healthcare stakeholders.
Développeur logiciel principal (React)/ Senior Software Developer (React)
IQVIA
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Full Time
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4 days ago
IQVIA
Design, develop, and maintain scalable web applications with a primary focus on React front-end development. Collaborate with cross-functional global teams to translate business requirements into technical architectures and provide high-level production support.
Build and maintain professional relationships with dental healthcare providers through digital channels and virtual platforms. Deliver educational presentations and execute targeted account plans to drive business growth and adoption of oral healthcare practices.
Develop and grow key healthcare accounts through virtual engagement with GPs, pharmacists, and public health stakeholders. Drive the adoption of smoking cessation solutions by delivering compliant product education and tailored business plans.
Manage end-to-end site start-up activities, including feasibility, identification, and activation for clinical trials. Coordinate ethics submissions, budget negotiations, and maintain communication between investigative sites and internal stakeholders.
Registered Dietician Clinical Trials Telehealth - Per Diem - New York
IQVIA
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Full Time
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5 days ago
IQVIA
Conduct nutritional assessments and develop individualized care plans for patients in clinical trials via telehealth. Monitor nutritional progress and maintain confidential clinical documentation for patients with rare and complex conditions.
Design, develop, and maintain web and native applications using C#, .NET, and Blazor for a medical practice management system. You will also implement REST interfaces, manage CI/CD pipelines, and ensure compliance with healthcare regulatory standards.
Tech Systems/Support Analyst - English + Dutch, French or German (Portugal Homebased)
IQVIA
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Full Time
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5 days ago
IQVIA
Provide first-level technical and operational support to Clinical Trials personnel via phone, email, and chat. Resolve routine technical issues and escalate complex problems to the appropriate support areas.
The role involves managing clinical trial start-up activities, including site identification, feasibility, and regulatory submissions in Portugal. The specialist acts as the primary contact for investigative sites to ensure compliance with SOPs and project timelines.
The Associate Consultant develops technology solutions and product specifications to meet business needs within the healthcare sector. They are responsible for conducting market research, managing stakeholders, and creating reports and presentations for clients.
Lead and coordinate global clinical trial management activities, ensuring successful planning, execution, and closure of trials. Serve as a key member of the Study Management Team to oversee compliance, quality, and timely delivery of milestones.
Provide country-level oversight of clinical trials from start-up through closeout, ensuring high-quality data delivery and regulatory compliance. Collaborate with cross-functional teams to manage study milestones, mitigate risks, and maintain inspection readiness.
The Director of Business Development is responsible for identifying and expanding relationships with life sciences organizations to drive growth in Content & Engagement solutions. This includes executing strategic growth plans, leading client presentations, and managing the full sales lifecycle from opportunity to contract.
The Inside Sales Representative is responsible for achieving sales forecasts and increasing product adoption by building relationships with targeted accounts and physicians. They handle inbound and outbound sales inquiries and coordinate strategies with teammates to maximize territory sales.
Lead the design, development, and deployment of scalable Generative AI and agentic systems for clinical and commercial life sciences applications. Provide technical leadership and mentorship while acting as a technical advisor for client engagements.
The role provides regulatory support and oversight for clinical trial submissions across global programs. Responsibilities include authoring regulatory documentation, managing submissions, and ensuring compliance throughout the clinical trial lifecycle.
Provide scientific and strategic epidemiology support for clinical development and drug safety activities within the Inflammation RWE team. Design and conduct observational research studies using real-world data to inform regulatory and clinical decisions.
Lead the delivery of clinical data management services for global projects, ensuring quality and budget compliance. Manage client relationships, financial aspects, and provide leadership to Data Team Leads.
Lead the vision, strategy, and roadmap for the Media OS platform to transform it into an AI-powered audience and activation ecosystem. Drive commercial growth and cross-functional leadership to deliver personalized, privacy-compliant healthcare marketing solutions.
Clinical Project Coordinator, IQVIA Biotech (Home-Based, Mexico)
IQVIA
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Full Time
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7 days ago
IQVIA
Support Project Leaders and Managers in coordinating clinical project activities, documentation, and tracking to ensure compliance with SOPs and GCP. Manage project communications, financial reports, and internal team meetings to meet quality and timeline metrics.
Leads product execution for identity-resolution and contextual intelligence capabilities by managing a team of Product Owners. Translates strategic direction into executable product plans and coordinates cross-functional teams to deliver customer value at scale.
Manage the full lifecycle delivery of eCOA projects, including scope, budget, and timeline monitoring for internal and external clients. Coordinate project teams across multiple time zones and serve as the primary liaison between technical staff and customers.
Accountable for the operational and scientific oversight, set-up, and delivery of assigned clinical trials at the regional and local level. This includes managing trial budgets, overseeing CRO activities, and ensuring compliance with GCP-ICH and local regulations.
Lead the development of optimum strategies for drug development, product lifecycle, and portfolio management to meet pharmaceutical customer goals. Provide high-level consultancy on clinical, regulatory, and commercial strategies from discovery to market.
Provide appropriate responses to inquiries from medical institutions and the general public while collecting and reporting adverse event information to clients. Perform supervisor duties including quality improvement, progress management, problem solving, and member support.
Manage end-to-end site start-up activities, including feasibility, identification, and activation for clinical trials. Coordinate ethics submissions, budget negotiations, and maintain communication with investigative sites and internal stakeholders.
Perform site monitoring visits including selection, initiation, and close-out while ensuring adherence to GCP and ICH guidelines. Manage study progress by tracking recruitment, regulatory approvals, and maintaining the Trial Master File.
The role involves enhancing and maintaining user interfaces for core applications while designing and debugging new UI features. Additionally, the developer will optimize the data transfer layer and collaborate on UI/UX planning and testing.
The role involves enhancing and maintaining user interfaces for core applications while designing and debugging new UI features. It also requires optimizing the data transfer layer between frontend and backend systems and conducting code reviews.
The expert defines and implements Clinical Electronic Data Capture (EDC) tools and processes aligned with trial protocols. This includes designing eCRF layouts, programming edit checks, and managing complex database integrations.
Act as a trusted advisor to Emerging Biopharma clients by developing and executing integrated commercialization and launch strategies. Lead senior-level client engagements to identify new business opportunities and ensure high-quality delivery of commercial solutions.
Senior Clinical Research Associate - Sponsor dedicated - Belgium - Home based (m/w/d)
IQVIA
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Full Time
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11 days ago
IQVIA
Perform site monitoring visits including selection, initiation, and close-out while ensuring adherence to GCP and ICH guidelines. Manage study progress by tracking regulatory submissions, subject recruitment, and data query resolution.
Clinical Research Associate II - Sponsor dedicated - Belgium - Home based (m/w/d)
IQVIA
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Full Time
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11 days ago
IQVIA
Perform site monitoring visits including selection, initiation, and close-out while ensuring adherence to GCP and ICH guidelines. Manage study progress by tracking regulatory submissions, subject recruitment, and data query resolution.
Maintain and update product reference databases for the Dutch market to ensure high data accuracy and quality. Collaborate with stakeholders to resolve data discrepancies and implement continuous improvement initiatives.
The CRA I is responsible for performing site selection, initiation, monitoring, and close-out visits for complex clinical trials. They ensure adherence to GCP and ICH guidelines while managing regulatory submissions and data query resolution.
Global Scientific Lead - Clinical Outcome Assessment (COA) Strategy Consulting - Multiple locations - Hybrid/Home-based
IQVIA
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Full Time
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12 days ago
IQVIA
Serve as the senior scientific authority for Clinical Outcome Assessment (COA) and Patient Experience Data (PED) strategies for pharmaceutical and biotechnology clients. Lead the scientific quality of deliverables, mentor multidisciplinary teams, and represent the company as an external thought leader in COA science.
Patient & Site Engagement Operations Manager - Sponsor Dedicated (m/w/d)
IQVIA
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Full Time
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13 days ago
IQVIA
Manage the coordination, planning, and implementation of patient recruitment and retention operational plans for clinical studies. Act as the primary operational contact for sponsors and manage project budgets and KPIs to ensure study milestones are met.
The Clinical Analyst partners with healthcare clients to operationalize CARE solutions by translating clinical requirements into system configurations and workflows. They act as a bridge between clinical users and internal product teams to drive improvements in patient outcomes and cost efficiency.
Principal, MedTech Consulting Services (Market Research & Consulting)
IQVIA
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Full Time
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13 days ago
IQVIA
Lead complex end-to-end market research and consulting engagements for global medical device and diagnostics companies. Drive business growth by owning personal sales targets and expanding client relationships through strategic IQVIA offerings.
Clinical Research Associate I - Sponsor dedicated - Netherlands - Home based (m/w/d)
IQVIA
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Full Time
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13 days ago
IQVIA
Perform site monitoring visits including selection, initiation, and close-out while ensuring adherence to GCP and ICH guidelines. Manage study progress by tracking regulatory submissions, subject recruitment, and data query resolution.
Clinical Research Associate II - Sponsor dedicated - Netherlands - Home based (m/w/d)
IQVIA
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Full Time
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13 days ago
IQVIA
Perform site monitoring visits including selection, initiation, and close-out while ensuring adherence to GCP and ICH guidelines. Manage study progress by tracking recruitment, regulatory approvals, and maintaining essential trial documentation.
Senior Clinical Research Associate - Sponsor dedicated - Netherlands - Home based (m/w/d)
IQVIA
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Full Time
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13 days ago
IQVIA
Perform site monitoring visits including selection, initiation, and close-out while ensuring adherence to GCP and ICH guidelines. Manage study progress by tracking recruitment, regulatory approvals, and maintaining essential trial documentation.
Lead end-to-end data management for complex global clinical trials from setup to database lock. Serve as the primary client contact while managing timelines, budgets, and mentoring junior staff.
Registered Dietician Clinical Trials Telehealth - Per Diem - North Carolina
IQVIA
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Full Time
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14 days ago
IQVIA
Conduct nutritional assessments and develop individualized care plans for patients in clinical trials via telehealth. Monitor nutritional progress and maintain confidential clinical documentation for patients with rare and complex conditions.
Lead the strategy, roadmap, and execution of data-driven personalization products to enable targeted omnichannel engagement for healthcare brands. Translate complex healthcare datasets into scalable, client-facing products while collaborating with engineering and data science teams.
Perform country-level site activation activities, including feasibility and maintenance for investigative sites in clinical trials. Prepare and track essential regulatory documents such as CDAs, ethics approvals, and Informed Consent Forms.
Serve as the single point of contact for feasibility, site activation, and maintenance activities for investigative sites. Manage regulatory submissions for the UK and Ireland while maintaining internal tracking systems and project plans.
Provides data management support and oversight for clinical trials, including the creation and tracking of deliverables like CRFs and data review plans. Collaborates with customers and partners to establish data expectations and ensure real-time inspection readiness for regulatory audits.
Lead end-to-end data management for complex global clinical trials from setup to database lock. Serve as the primary client contact while overseeing data reconciliation, budgets, and the mentoring of junior staff.
The Analyst provides operational and strategic support for life sciences client engagements, focusing on commercial effectiveness and market assessments. They process large data sets to generate actionable insights and contribute to the development of client presentations and workshops.
Lead end-to-end data management for complex global clinical trials from setup to database lock. Serve as the primary client contact while overseeing data reconciliation, budgets, and the mentoring of junior staff.
Lead end-to-end data management for complex global clinical trials from setup to database lock. Serve as the primary client contact while managing timelines, budgets, and mentoring junior staff.
Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)
IQVIA
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Full Time
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19 days ago
IQVIA
Lead cross-functional clinical trial teams to plan and manage clinical studies end-to-end. Accountable for operational planning, budget oversight, and the delivery of high-quality study documentation and reports.
The role involves providing technical expertise to develop and support eCOA business systems and solutions for clients. Responsibilities include defining system scope, documenting user requirements, and guiding less-experienced analysts.
The Project Lead is responsible for the delivery of clinical studies, ensuring they meet contractual requirements, quality standards, and financial goals. This includes managing cross-functional teams, handling customer relationships, and overseeing project risks and milestones.
The SES Project Lead optimizes the delivery of Site Enablement Solutions throughout the project lifecycle, managing budgets and serving as an internal consultant. They coordinate with stakeholders to implement operational plans and ensure the quality of deliverables for clinical trials.
Therapeutic Strategy Lead - Internal Medicine/Immunology , Home-Based (m/w/d)
IQVIA
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Full Time
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20 days ago
IQVIA
Develop and implement tailored delivery strategies for customers during the RFP and Bid Defense cycle to drive business growth. Bridge the gap between sales, medical, and operational teams to ensure seamless project execution and strategic alignment.
Serve as the primary account manager for COA Accelerator clients, overseeing onboarding, training, and ongoing support. Drive customer success by monitoring engagement, collecting feedback for product enhancements, and identifying business expansion opportunities.
The role involves serving as the Single Point of Contact for investigative sites and ensuring adherence to standard operating procedures and project timelines. Responsibilities include performing site activation activities, preparing regulatory documents, and maintaining internal systems.
Manage site activation activities and serve as the single point of contact for investigative sites and project management teams. Ensure all regulatory, ethics, and informed consent documents are accurately prepared and approved according to project timelines.
Epidemiologist, Internal Medicine, Inflammation & Immunology (FSP Sponsor Dedicated)
IQVIA
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Full Time
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24 days ago
IQVIA
Provide scientific support for RWE/Epidemiology studies through literature reviews, data cleaning, and the development of scientific deliverables. Coordinate operational activities and oversee vendor deliverables to ensure high-quality study execution.
Clinical Project Coordinator, IQVIA Biotech (Home-Based, Brazil)
IQVIA
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Full Time
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25 days ago
IQVIA
Support Project Leaders and Managers in coordinating clinical project activities, documentation, and financial tracking. Ensure compliance with SOPs, GCP, and regulatory requirements while maintaining project timelines and customer satisfaction.
Develop, maintain, and optimize data management applications and database check algorithms using C++, PHP, and SQL. Collaborate with teams in agile routines to implement technical solutions and provide 3rd-level support.
Lead and execute advanced clinical and operational analytics to generate deep insights from disparate data sources. Develop scalable machine learning models and robust code to solve complex business problems.
Develop and implement corporate architecture and strategies in collaboration with international teams and management. Analyze existing systems to create innovative software solutions while ensuring compliance with regulatory requirements and engineering standards.
The role involves conducting online meetings and developing tailored communication materials to maximize sales growth for a pharmaceutical project. It also requires managing appointments, performing sales calls, and providing accurate daily reports.
The role involves managing site activation activities, including preparing regulatory documents and ensuring adherence to SOPs and project timelines. The specialist serves as the single point of contact for investigative sites and project management teams to ensure successful study start-up.
Serve as the single point of contact for site feasibility, activation, and maintenance activities for investigative sites. Review and track regulatory documents, contracts, and ethics approvals while maintaining internal project tracking systems.
Identify and target new large and medium-sized MedTech customers to drive revenue growth through IQVIA's suite of data, analytics, and consulting services. Manage overall relationships with key executives and oversee the full sales cycle from prospecting to contract execution.
Drive revenue growth among publisher clients by utilizing consultative sales strategies and deep product expertise. Collaborate with cross-functional teams to identify opportunities, recruit new partners into the Healthcare Communications Network, and optimize solution performance.
Care Managers contact insurance companies to perform benefit investigations, verify eligibility, and manage prior authorizations or appeals. They also communicate with patients and providers to facilitate enrollment in assistance programs and support treatment adherence.
Director, Solution Sales, Small Pharma Segment Lead, IQVIA Digital (Remote)
IQVIA
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Full Time
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a month ago
IQVIA
Lead and develop a team of Solution Sellers to drive growth across digital engagement solutions for small and emerging biopharma segments. Define go-to-market strategies and collaborate with internal product teams to enhance segment-specific offerings.
Lead the design and development of innovative therapeutic and operational strategies for internal medicine programs to secure new business. Collaborate with cross-functional teams to translate these strategies into actionable delivery plans and maintain high-level client relationships.
Responsible for reviewing domestic and international literature and conference abstracts to determine if safety information needs to be reported. This includes performing QC, entering data into monitoring systems and Argus, and preparing research reports for PMDA submission.
Manage the full lifecycle of eCOA projects, including scope, budget, timelines, and deliverables for internal and external clients. Coordinate project teams across multiple locations and maintain strong customer relationships to ensure high-quality service delivery.
The Principal Statistical Programmer is responsible for reviewing submission-ready datasets, tables, figures, and listings. They lead the design and implementation of complex SAS programs and oversee the delivery of integrated summaries of safety and efficacy.
The Principal Statistical Programmer leads the design, development, and quality control of SAS programs for clinical data submission packages. They oversee the creation of ADaM datasets, tables, figures, and listings while collaborating with study teams to ensure regulatory compliance.
The Senior Statistical Programmer is responsible for designing and reviewing submission-ready datasets, tables, figures, and listings in ADaM format. They lead the development of complex SAS programs and oversee pooled and exploratory analyses to ensure clinical data accuracy for regulatory submission.
The Principal Statistical Programmer leads the design and development of SAS programs for clinical data analysis and submission packages. They are responsible for ensuring the quality and accuracy of ADaM datasets, tables, figures, and listings for regulatory submission.
The Senior Medical Director provides medical, clinical, and scientific advisory expertise for oncology and hematology trials, focusing on medical monitoring and strategic input. Responsibilities include reviewing protocols, managing patient safety, and supporting business development activities for complex multi-region studies.
Responsible for the end-to-end investigator and site payment process for clinical trials in the US and Canada. This includes managing purchase orders, processing invoices through CTMS, and resolving payment queries for stakeholders.
The Senior Statistical Programmer is responsible for designing and reviewing submission-ready datasets, tables, figures, and listings. They lead the development of complex SAS programs and oversee pooled and exploratory analyses to ensure high-quality clinical trial deliverables.
Tech/Systems Support Analyst - Spanish Native/English Fluent (Portugal Homebased)
IQVIA
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Full Time
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a month ago
IQVIA
Provide first-level technical support for workstations and applications for internal and external customers. Resolve routine technical problems and escalate complex issues to the appropriate support areas.
The Senior Statistical Programmer is responsible for designing and reviewing submission-ready datasets, tables, figures, and listings. They lead the development of complex SAS programs and oversee pooled and exploratory analyses for clinical trials.
Define and lead the AI strategy and architecture for the MediaOS platform, focusing on personalization, recommendation systems, and scalable ML pipelines. Establish MLOps best practices and integrate emerging technologies like Generative AI and LLMs into the platform.
Director, Solution Sales – Large & Mid Pharma Segment Lead, IQVIA Digital (Remote)
IQVIA
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Full Time
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a month ago
IQVIA
Lead and develop a team of Solution Sellers to drive commercial strategy and revenue growth for Large and Mid-Sized pharmaceutical clients. Partner with internal product and analytics teams to evolve digital engagement solutions and serve as a strategic advisor to senior client executives.
Provide strategic medical and scientific expertise in hematology-oncology to support proposal development, protocol design, and clinical development plans. Act as a subject matter expert and consultant throughout the research and development lifecycle to guide project teams and sponsors.
Coordinate all aspects of medical education programs, including venue sourcing, speaker travel, and attendee recruitment. Ensure all programs are executed accurately and compliantly according to client budgetary and regulatory guidelines.
Senior Epidemiologist, Inflammation, RWE & Regulatory Strategy (FSP Sponsor Dedicated)
IQVIA
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Full Time
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a month ago
IQVIA
Design and execute real-world evidence studies to inform clinical development strategy and address regulatory safety questions for Phase 2 and 3 programs. Provide scientific oversight for complex observational research using commercial real-world data platforms.
Manage contract strategy and oversee all start-up contracting activities for biotech sponsors, including the development of investigator grant estimates and budget templates. Collaborate with stakeholders and regional teams to ensure compliance, operational excellence, and the achievement of financial targets.
Lead and develop a team of Project Managers responsible for the end-to-end delivery of device logistics for eCOA and eConsent clinical technologies. Coordinate with cross-functional teams and third-party vendors to ensure the timely provisioning, deployment, and recovery of devices globally.
Manage the timely collection of customer debt for French and Northern European accounts while maintaining strong client relationships. Coordinate the resolution of payment queries and report credit risk red flags to the Global Risk Team.
Serve as the primary account manager for COA Accelerator clients, overseeing onboarding, training, and ongoing support to drive customer success. Collaborate with product teams to enhance platform features based on client feedback and support business development initiatives.
Care Managers contact insurance companies to perform benefit investigations, verify eligibility, and manage prior authorizations or appeals. They also communicate with patients and providers to facilitate enrollment in assistance programs and support treatment adherence.
Senior Epidemiologist, HIV Treatment, Retrospective Claims Study Expertise (FSP Sponsor Dedicated)
IQVIA
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Full Time
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a month ago
IQVIA
Design and conduct epidemiological studies to generate real-world evidence, focusing on treatment patterns and clinical outcomes. Lead the development of study protocols, analysis plans, and reports to support regulatory and internal decision-making.
Therapeutic Strategy Lead - Internal Medicine/Immunology (Home-Based)
IQVIA
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Full Time
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a month ago
IQVIA
Develop and implement tailored delivery strategies for customers during the RFP and Bid Defense cycle to drive business growth. Bridge the gap between sales, medical, and operational teams to ensure seamless project execution and strategic alignment.
The role involves managing clinical trial start-up activities, including EU-CTR compilation and regulatory submissions for investigative sites in Belgium. The specialist will act as the primary contact for sites, ensuring compliance with ICH-GCP and project timelines.
The Product Owner is responsible for developing the product vision and roadmap while translating business requirements into user stories. They act as the central interface between stakeholders and international offshore development teams to optimize AI-driven healthcare solutions.
Oversee clinical trial management teams to ensure the delivery of project objectives regarding speed, quality, and cost. Act as the primary point of contact for clients while managing operational aspects, recruitment metrics, and data integrity.
Therapeutic Strategy Lead - Internal Medicine/Immunology (Home-Based)
IQVIA
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Full Time
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a month ago
IQVIA
Develop and implement tailored delivery strategies for the RFP/Bid Defense cycle to differentiate the company from competitors. Bridge the gap between sales, medical, and operational teams to ensure seamless project execution and business growth.
The Associate Site Activation Manager designs and implements strategies for site activation from award to enrollment. They lead country operations teams to ensure client commitments are delivered on time, within scope, and according to budget.
Lead the strategic and operational delivery of global site activation activities to accelerate patient enrollment. This includes managing site identification, regulatory submissions, and contracting in compliance with ICH-GCP standards.
Therapeutic Strategy Lead - Internal Medicine/Immunology (Home-Based)
IQVIA
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Full Time
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a month ago
IQVIA
Develop and implement tailored delivery strategies for customers during the RFP and Bid Defense cycle. Bridge the gap between sales, medical, and operational teams to ensure seamless project execution and business growth.
Manage start-up contracting activities, including developing investigator grant estimates and proposal text for biotech sponsors. Ensure compliance with regulatory requirements and maintain internal tracking systems like CTMS to meet project timelines.
Attaché de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology
IQVIA
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Full Time
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a month ago
IQVIA
The CRA II monitors Phase I-IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. Responsibilities include conducting site visits, training personnel, and managing site activities from start-up to close-out.
Therapeutic Strategy VP, Infectious Disease/Respiratory (Home - Based)
IQVIA
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Full Time
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a month ago
IQVIA
The Therapeutic Strategy VP creates integrative product development strategies for pharmaceutical products from discovery to market. This includes overseeing preclinical, clinical, regulatory, and commercial strategies while leading clinical trial design for various clients.
The Regional Specialist coordinates remote clinical visits by onboarding sites and clinicians and managing visit logistics. They serve as the primary liaison between internal study teams, nurses, and investigator sites to ensure project schedules and compliance are met.
Provide medical, clinical, and scientific advisory expertise for clinical trials, focusing on medical monitoring and patient safety. Support business development activities by developing medical strategies and contributing to client proposals and bid defenses.
Responsible for study build, design, and system configurations, including the creation of eCRF and edit specifications. The role also manages project financials from a programming shared services perspective and collaborates with various clinical stakeholders.
Maintain and drive growth for priority accounts by maximizing opportunities through successful negotiation. Collaborate with internal and external stakeholders to defend and expand specific pharmaceutical accounts.
Drive the growth of the Cell and Gene Therapy portfolio by developing innovative, data-driven clinical trial strategies and solutions. Provide scientific expertise for business development, protocol design, and thought leadership activities including publications and presentations.
The Medical Director serves as the medical expert and monitor for clinical research trials focusing on rheumatologic disorders. Responsibilities include providing scientific guidance to project leaders, managing adverse events, and contributing to the medical strategy of client proposals.
The role involves reviewing structured clinical patient data to ensure medical plausibility, protocol adherence, and overall completeness for clinical trials. Responsibilities include identifying data anomalies, reviewing inclusion/exclusion criteria, and verifying adverse events and laboratory results.
Manage site activation activities and serve as the single point of contact for investigative sites and project management teams. Ensure all regulatory, ethics, and contractual documents are accurately prepared and executed according to project timelines.
Manage site activation activities and serve as the single point of contact for investigative sites and project management teams. Ensure all regulatory, ethics, and contractual documents are accurately prepared and executed according to project timelines.
Lead business development and account management for MedTech clients to deliver revenue targets and strengthen long-term strategic engagements. Orchestrate integrated end-to-end solutions by leveraging internal networks and building relationships with senior client executives.
Lead the Audience Ingestion team in onboarding, validating, and maintaining audience data across the digital organization. Drive the standardization and automation of ingestion workflows to support measurement, targeting, and downstream delivery.
The Associate Laboratory Project Set-up Manager leads the design and launch of clinical research studies, ensuring high-quality study start-up deliverables. This role involves coordinating effectively with sponsors, CROs, and internal laboratory teams.
The role involves performing site selection, initiation, monitoring, and close-out visits while maintaining essential documentation. Responsibilities also include managing subject recruitment, tracking regulatory submissions, and ensuring the quality and integrity of site practices.
The role involves performing site selection, initiation, monitoring, and close-out visits while maintaining essential documentation. Responsibilities also include managing subject recruitment, tracking regulatory submissions, and ensuring the quality and integrity of site practices.
The Site Activation Specialist serves as the single point of contact for investigative sites and project teams to manage site start-up activities. Responsibilities include preparing regulatory documents, tracking approvals, and ensuring adherence to SOPs and project timelines.
Senior Account Manager, Platform Success - IQVIA Digital (REMOTE)
IQVIA
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Full Time
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2 months ago
IQVIA
The Senior Account Manager serves as the strategic relationship owner for platform clients, ensuring success through proactive leadership and executive engagement. They are responsible for designing multi-channel programmatic strategies and translating client goals into actionable media plans to maximize ROI.
The Clinical Specialist reviews psychiatric scales and provides guidance to raters on methodology and scoring techniques. They ensure the integrity of clinical trial data through functional assessments and mock interviews.
The Clinical Specialist ensures the integrity of clinical trial data by reviewing assessment scales and providing guidance to raters. Responsibilities include evaluating assessment quality, conducting live feedback sessions, and supporting rater performance through mock interviews.
Manage contract strategy and oversee all start-up contracting activities for selected sponsors, including complex studies and multi-protocol programs. Develop investigator grant estimates, maintain contract templates, and collaborate with stakeholders to ensure compliance and operational excellence.
Provide statistical consulting and technical support for the design, analysis, and regulatory submission of clinical trial studies. Act as a statistical team lead managing scope, budgets, and collaboration with medical and programming staff for reporting.
Associate Director, Product Management - Contracting (CTFS) (Remote)
IQVIA
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Full Time
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2 months ago
IQVIA
Lead the strategy, delivery, and launch of the Contracting module within the Clinical Trial Financial Suite (CTFS) SaaS platform. Coordinate cross-functionally with engineering, design, and sales to translate complex financial and clinical needs into scalable product solutions.
The Associate Director will lead the design and implementation of global security architecture, focusing on cloud environments and Zero Trust initiatives. They will collaborate with stakeholders to integrate security by design and manage the evaluation and deployment of enterprise security platforms.
The Clinical Data Management Lead serves as the primary point of contact for customers, managing large global studies and ensuring high-quality data deliverables. They provide leadership to data operations teams, manage budgets, and drive process improvements while serving as a subject matter expert.
The Clinical Data Management Lead serves as the primary point of contact for customers, managing large global studies and providing leadership to data management teams. They are responsible for overseeing project deliverables, ensuring process improvements, managing budgets, and serving as a subject matter expert for data management tasks.
Data Analyst (SAS / SQL Programming) - German Speaker (Spain remote)
IQVIA
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Full Time
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2 months ago
IQVIA
Perform strategic qualitative and quantitative analyses to derive actionable insights for pharmaceutical and healthcare clients. Collaborate with project managers and business intelligence units to create reports, presentations, and project deliverables.
You will design and develop software solutions using .NET and Java to support business processes and customer requirements. Additionally, you will be responsible for the technical architecture, performance optimization, and quality assurance of existing software systems.
Team Lead Software Development for KV Solutions (m/w/d) full remote
IQVIA
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Full Time
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3 months ago
IQVIA
You will provide professional and organizational leadership for a growing development team of approximately 20 employees. Additionally, you will define software architecture standards, manage the technological roadmap, and oversee complex software projects.
Spanish Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - Missouri
IQVIA
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Full Time
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3 months ago
IQVIA
Conduct nutritional assessments via telehealth and develop individualized dietetic care plans for patients in clinical trials. Provide ongoing dietary counseling and monitor patient progress while maintaining accurate clinical documentation.
Spanish Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - Nevada
IQVIA
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Full Time
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3 months ago
IQVIA
Conduct nutritional assessments and develop individualized dietetic care plans for patients via telehealth. Provide ongoing dietary counseling and monitor patient progress and adherence within clinical research studies.
Spanish Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - North Carolina
IQVIA
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Full Time
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3 months ago
IQVIA
Conduct nutritional assessments and develop individualized dietetic care plans for patients via telehealth. Monitor patient progress and adherence while maintaining accurate clinical documentation for clinical research studies.
Spanish Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - Washington
IQVIA
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Full Time
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3 months ago
IQVIA
Conduct nutritional assessments and develop individualized dietetic care plans for patients via telehealth. Provide ongoing dietary counseling and monitor patient progress and adherence within clinical research studies.
Spanish Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - Idaho
IQVIA
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Full Time
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3 months ago
IQVIA
Conduct nutritional assessments and develop individualized dietetic care plans for patients via telehealth. Provide ongoing dietary counseling and monitor patient progress and adherence within clinical research studies.
Perform site selection, initiation, monitoring, and close-out visits while ensuring compliance with GCP and ICH guidelines. Manage study progress by tracking regulatory submissions, recruitment, and data integrity across various therapeutic areas.
The Key Account Representative is responsible for managing and expanding relationships with healthcare providers and systems within an assigned territory to meet sales goals. This role involves executing strategic sales activities, conducting in-person calls with decision-makers, and collaborating with internal teams to ensure client satisfaction.
The role involves performing site selection, initiation, monitoring, and close-out visits while maintaining accurate documentation. You will also manage study progress by tracking regulatory submissions, recruitment, and data query resolution.
Senior Clinical Research Associate, Early Clinical Development
IQVIA
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Full Time
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3 months ago
IQVIA
The Senior CRA is responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. They conduct site visits, support subject recruitment, and maintain essential study documentation to ensure data integrity.
The Principal Biostatistician provides statistical support for clinical trials, including authoring statistical analysis plans and producing efficacy analysis datasets. They also collaborate with multi-disciplinary teams and contribute to regulatory documents such as INDs and NDAs.
The nurse will provide direct support in nursing consultations and coordinate patient care with other specialized services like psychology and nutrition. This role focuses on improving patient quality of life, functional autonomy, and therapeutic adherence within a patient support program.
Registered Dietician Clinical Trials Telehealth - Per Diem - Kentucky
IQVIA
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Full Time
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3 months ago
IQVIA
The Registered Dietitian will conduct nutritional assessments and develop individualized care plans for patients via telehealth. They will also provide ongoing dietary counseling and monitor patient progress within clinical research studies.
Registered Dietician Clinical Trials Telehealth - Per Diem - Tennessee
IQVIA
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Full Time
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3 months ago
IQVIA
The Registered Dietitian will conduct nutritional assessments and develop individualized care plans via telehealth for patients in clinical trials. They will provide ongoing dietary counseling and monitor patient progress while maintaining accurate clinical documentation.
Principal Enterprise Architect - Mergers & Acquisitions (Remote)
IQVIA
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Full Time
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3 months ago
IQVIA
The Principal Enterprise Architect will lead architectural strategy for mergers and acquisitions, including technology due diligence and integration planning. They will drive application portfolio rationalization and establish scalable architecture patterns to support high-velocity M&A activities.
The Solution Sales Specialist identifies and advances revenue opportunities for IQVIA's strategy and analytics portfolio within the hospital and health systems industry. They partner with client leaders to provide actionable insights and manage the full sales cycle from proposal to implementation.
The role involves administering clinical assessments to trial participants and evaluating the quality of assessments performed by other raters. You will ensure data reliability through standardized methodology, provide feedback on scoring techniques, and maintain accurate documentation of all interactions.
The role involves performing clinical programming tasks for Phase I-IV trials using SAS, Python, and other tools while adhering to client SOPs. Responsibilities include creating technical specifications, managing SDTM datasets, and supporting risk-based monitoring and regulatory submissions.
Senior Clinical Research Associate, Sponsor dedicated in Poland
IQVIA
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Full Time
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3 months ago
IQVIA
Perform site selection, initiation, monitoring, and close-out visits while ensuring compliance with GCP and ICH guidelines. Manage study progress by tracking regulatory submissions, recruitment, and data integrity.
The representative will serve as the primary contact for patients and healthcare professionals to assist with payment programs, card activation, and eligibility. They are responsible for documenting resolutions and troubleshooting submission rejections via phone, email, or fax.
Perform site monitoring and management to ensure study protocols, regulatory requirements, and GCP/ICH guidelines are strictly followed. Manage study progress by tracking regulatory submissions, recruitment, data integrity, and site documentation.
Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - Florida
IQVIA
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Full Time
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3 months ago
IQVIA
Conduct nutritional assessments and develop personalized dietetic plans for clients via telecommunications. Provide ongoing dietetic counseling and support to clients and their families while maintaining accurate records.
The Site Activation Specialist will manage site activation activities, including contract negotiations and regulatory document tracking, in accordance with SOPs and project timelines. They serve as the primary point of contact for investigative sites and internal project teams to ensure quality deliverables.
Registered Dietitian – Clinical Research Support (South Korea)
IQVIA
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Full Time
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3 months ago
IQVIA
The Registered Dietitian will conduct comprehensive nutritional assessments and provide ongoing counseling and motivational support to study participants. They will monitor participant progress and collaborate with the clinical research team to ensure adherence to study protocols.
The Registered Dietitian will conduct comprehensive nutritional assessments and provide ongoing counseling and motivational support to study participants. They will monitor participant progress and collaborate with the clinical research team to ensure adherence to study protocols.
The Registered Dietitian will conduct comprehensive nutritional assessments and provide ongoing counseling and motivational support to study participants. They will monitor participant progress and collaborate with the clinical research team to ensure adherence to study protocols.
The Medical Writer will be responsible for creating clinical trial-related documents such as protocols, clinical study reports, and CTD modules, as well as authoring post-marketing surveillance documents and clinical study reports/papers. They will also perform Quality Control (QC) checks on various documents.
The Lead Medical Writer will be responsible for creating and reviewing clinical trial documents such as protocols, CSRs, and CTDs, as well as adapting global protocols for Japanese requirements. Responsibilities also include managing projects, resources, budgets, client interactions, and mentoring junior staff.
Medical Biller/Claims Processing - Patient Support Representative (Remote; 10am-7pm EST)
IQVIA
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Full Time
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4 months ago
IQVIA
The primary responsibilities involve receiving medical claims from healthcare providers or patients, ensuring all necessary supporting documentation is present, and interpreting the Explanation of Benefits (EOB) or CMS1500 form. The representative must vet the claim against program-specific business rules to ultimately decide whether the claim should be paid or rejected.
The developer will design, develop, and deliver modern software solutions across the full application stack, including front-end, back-end, cloud, and databases. Key tasks involve migrating regional systems to global Azure components, optimizing performance, and leading medium-scale development initiatives.
Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italy
IQVIA
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Full Time
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4 months ago
IQVIA
The Clinical Research Associate will perform monitoring and site management to ensure studies adhere to protocols, regulations, and sponsor requirements, including conducting site visits for selection, initiation, monitoring, and close-out.
Spanish Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - Indianapolis
IQVIA
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Full Time
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4 months ago
IQVIA
Remote Registered Dieticians are responsible for conducting nutritional assessments and developing personalized dietetic plans for clients with various disease classifications via telecommunications. They must also provide ongoing dietetic counseling and support to clients and their families while maintaining accurate and confidential client records.
CRA II or SrCRA I (m/w/d), Single Sponsor, home-based Austria
IQVIA
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Full Time
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4 months ago
IQVIA
Responsibilities include performing site selection, initiation, monitoring, and close-out visits while supporting the development of subject recruitment plans. The role also involves evaluating site quality against GCP/ICH guidelines and managing progress through tracking submissions, recruitment, and data query resolution.
This role involves participating in end-to-end site management, from feasibility through site closure, acting as the main contact for investigative sites and study team members. Key duties include supporting site qualification, obtaining regulatory green lights, and managing site maintenance and close-out activities.
This role serves as the first point of contact for technical support and inquiries regarding systems, platforms, and related technologies used in clinical trials, providing high-quality, accurate, and compliant support to Japanese market users. Key duties include initial technical troubleshooting, guiding users, classifying inquiries, triaging issues like AE/PQC, and accurately documenting all interactions according to IQVIA standards.
Associate Director Senior Study Lead - Single Sponsor Dedicated
IQVIA
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Full Time
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4 months ago
IQVIA
The Associate Director Senior Study Lead guides the planning and end-to-end management of assigned clinical studies, acting as the leader of the cross-functional clinical trial team (CTT). This role is accountable for proactive operational planning, overseeing budget and resource allocation, and fostering an empowered organization capable of navigating a matrix environment.
The Flex Nurse Educator delivers essential remote educational support and medication training to patients with chronic diseases via various virtual channels, providing in-person education only when covering territory vacancies. Key duties include facilitating connections to approved resources, encouraging dialogue between patients and healthcare providers, and maintaining accurate documentation while upholding compliance standards.
The role involves directly administering assessments to clinical trial participants or evaluating the quality of assessments performed by others, providing feedback on interview technique and scoring to ensure data reliability. Responsibilities also include evaluating case data, conducting live interactions with raters for guidance, and completing all assigned tasks and documentation timely.
The role involves conducting comprehensive nutritional assessments and providing ongoing counseling and motivational support to participants in international clinical studies focused on metabolic diseases. Responsibilities also include monitoring participant progress and collaborating with the clinical research team to ensure adherence to study protocols.
The Flex Nurse Educator delivers essential remote educational support and medication training to patients with chronic diseases using various virtual platforms. This role also provides in-person education exclusively during territory vacancy coverage while maintaining high educational standards and compliance.
The Flex Nurse Educator delivers remote patient education and medication training, primarily through virtual channels. They also provide in-person support during territory coverage, ensuring compliance and maintaining educational standards.
The Principal Statistical Programmer develops and validates complex datasets and outputs using SAS programming, ensuring compliance with CDISC standards like ADaM and SDTM models. This role also involves collaborating with cross-functional teams, providing technical guidance, and mentoring junior programmers.
Typical responsibilities involve performing site selection, initiation, monitoring, and close-out visits, along with maintaining necessary documentation and supporting the development of a subject recruitment plan. The role also includes establishing communication lines, administering protocol training, evaluating site quality, and managing progress tracking for submissions, recruitment, and data resolution.
The role involves conducting targeted sales calls to dental professionals and managing territory activities to drive sales performance. Additionally, the representative will engage in professional education and support initiatives to build strong partnerships within the dental community.
The Sales Lead will lead field-based activities across Gauteng, conducting high-quality sales calls and delivering professional detailing. They will also engage with dental professionals and manage territory budgets while providing exceptional customer service.
The Clinical Data Team Lead will manage the end-to-end delivery of data management services for projects, ensuring quality deliverables on time and within budget. They will serve as the primary point of contact for clients and provide project management expertise while maintaining strong customer relationships.
Flex Nurse Educator - Spokane, WA (Must have/obtain CA license)
IQVIA
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Full Time
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7 months ago
IQVIA
The Flex Nurse Educator delivers remote patient education and medication training, primarily through virtual channels. They also provide in-person support during territory coverage while maintaining compliance and educational standards.
The Flex Nurse Educator delivers remote patient education and medication training, primarily through virtual channels. They also provide in-person support during territory coverage, ensuring compliance and continuity of care.
The Flex Nurse Educator delivers remote patient education and medication training, primarily through virtual channels. They also provide in-person support during territory coverage while maintaining compliance and educational standards.
The Flex Nurse Educator delivers educational support and medication training to patients with chronic diseases primarily through virtual channels. They also provide in-person education during territory coverage while maintaining compliance and program standards.
The Flex Nurse Educator delivers educational support and medication training to patients with chronic diseases primarily through virtual channels. They also provide in-person education during territory coverage and maintain compliance with program guidelines.
Spécialiste en validation et en tests de systèmes / System Validation and Testing Specialist
IQVIA
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Full Time
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8 months ago
IQVIA
The specialist designs, develops, implements, and updates software systems according to organizational needs. They conduct thorough testing to ensure software functionality and document any issues found.
As a Clinical Specialist Consultant, you will ensure the reliability and standardization of assessments in clinical trials. Responsibilities include reviewing scales, conducting patient assessments, and evaluating rater performance.
The Flex Nurse Educator delivers educational support and medication training to patients with chronic diseases primarily through virtual channels. They also provide in-person education during territory coverage while maintaining compliance and high educational standards.
Flex Nurse Educator - Anchorage, AK (Must have/obtain CA license)
IQVIA
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Full Time
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8 months ago
IQVIA
The Flex Nurse Educator delivers educational support and medication training to patients with chronic diseases primarily through virtual channels. They also provide in-person education during territory coverage while maintaining compliance and program standards.
Agent de centre d'appels / Call Center Agent Bilingual French/English
IQVIA
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Full Time
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9 months ago
IQVIA
The Call Center Agent will conduct inbound and outbound calls to notify potentially affected facilities and maintain a high level of professionalism and confidentiality. They will also manage data entry and perform general clerical duties.
The Project Manager III will write requirements for assigned IRT studies and manage their implementation to ensure patients receive the correct study drug according to the Sponsor’s protocol. This role involves consulting with clients, managing timelines, and overseeing user acceptance testing.
The Site Payments Analyst ensures accurate and timely payments to clinical trial sites by monitoring payable items and validating invoices against completed services. They also participate in trial oversight meetings and coordinate with contract managers to maintain accurate payment terms.
Lead and coordinate software delivery across IQVIA Connected Devices’ product teams, ensuring alignment of timelines, dependencies, risk management strategies, and release milestones. Act as a central point of contact for delivery status, blockers, and escalation across teams.
