Lead the design and development of enterprise-grade Power BI dashboards and reporting solutions. Partner with BI engineers to optimize data structures and translate business requirements into technical data designs.
IQVIA
231 Remote Job Openings at IQVIA
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.
Perform daily administrative activities to support the improvement of clinical trial processes and optimize monitoring and start-up SOPs. Act as a central contact for client directors and mentor less experienced Clinical Process Assistants.
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 managing project timelines for investigative sites.
Design and develop software solutions to integrate medical devices into the ClinSpark platform for seamless data flow. Contribute to full-stack development, system validation, and the creation of technical documentation within a global engineering team.
The role involves reviewing RFPs to develop strategic proposals, budgets, and scopes of work for customers. It also requires coordinating with internal stakeholders to ensure document quality and maintaining corporate tracking databases.
The Inside Sales Representative is responsible for achieving sales forecasts and increasing product adoption by building relationships with targeted accounts and physicians. This includes managing inbound and outbound sales calls and coordinating strategies with teammates to maximize territory sales.
The role involves supporting the sales team by managing customer inquiries and streamlining the process from initial quote to signed sales order. It also requires maintaining CRM accuracy and coordinating with internal pricing teams to support enterprise client accounts.
Perform country-level site activation activities, including feasibility and maintenance, in accordance with local and international regulations. Manage the preparation, tracking, and approval of essential site documents such as CDAs, regulatory filings, and Informed Consent Forms.
The role involves reviewing patient-level clinical and safety data to ensure medical accuracy and completeness. It also requires preparing aggregated data visualizations and collaborating with study physicians to support medical evaluations.
Data Analyst (KPIs & Reporting) - Excel & SQL / Madrid Homebased
IQVIA
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Full Time
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3 days ago
IQVIA
The role is responsible for the quality assurance and control of data within retail and hospital reporting offerings. It involves monitoring team performance, updating quality KPIs, and improving QA processes through collaboration with local offices.
Support Sales, Finance, and GBO teams with contract and proposal processes, including work allocation and system updates. Manage product updates in Salesforce and process proposal budgets while running ad-hoc compliance reports.
The Contracts Manager is responsible for drafting, reviewing, and redlining legal and business terms for commercial services within the US business unit. They manage a high volume of contracts of various complexities while collaborating with stakeholders to implement contracting efficiencies.
Develop and prepare contracts and budgets for assigned customers to support the global sales team. Collaborate with project teams to define terms, conditions, and scope of work while maintaining contract databases.
Lead the development of innovative therapeutic and operational strategies for respiratory clinical trials to secure new business and increase market share. Drive early client engagement and lead cross-functional teams through the proposal process to award and subsequent delivery translation.
Lead a core engineering organization responsible for audience and data platforms, overseeing delivery and technical direction. Drive the architecture of APIs and data pipelines while managing a distributed team of managers and engineers.
Establish and lead the Data Security Architecture practice by defining strategies for data discovery, classification, and protection across a hybrid multi-cloud environment. Develop security guardrails for AI/ML pipelines and ensure alignment with global regulatory requirements and enterprise data governance.
Epidemiologist, Internal Medicine, Inflammation & Immunology (FSP Sponsor Dedicated)
IQVIA
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Full Time
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4 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.
Lead the strategy, roadmap, and execution of data-driven personalization products to enable targeted omnichannel engagement for healthcare brands. Translate complex healthcare datasets and behavioral signals into scalable, client-facing SaaS products.
Clinical Project Coordinator, IQVIA Biotech (Home-Based, Mexico)
IQVIA
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Full Time
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4 days ago
IQVIA
Support Project Leaders and Clinical Project Managers in managing project documentation, tracking metrics, and ensuring compliance with SOPs and GCP. Coordinate internal and customer meetings, manage project finance reports, and oversee study-specific training.
Clinical Project Coordinator, IQVIA Biotech (Home-Based, Brazil)
IQVIA
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Full Time
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4 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.
The specialist is responsible for receiving and documenting lifecycle safety data and product inquiries from patients and healthcare providers. This includes creating adverse event and product quality complaint reports while ensuring compliance with regulatory guidelines and SOPs.
Associate Director, Sales Enablement - AI & Technology Solutions
IQVIA
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Full Time
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4 days ago
IQVIA
Build and lead the Sales Enablement function for AI & Technology Solutions to accelerate growth and improve go-to-market effectiveness. Translate complex product capabilities into clear business value, repeatable sales motions, and high-impact enablement assets.
Lead a high-performing data analytics team to design and scale production-grade data solutions for healthcare and life sciences. Own the end-to-end delivery of analytics products, including governance, cloud operationalization, and strategic client relationship management.
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.
Review and process safety data and adverse events in compliance with regulations and SOPs. Liaise with healthcare professionals and internal teams to ensure quality and productivity standards are met.
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.
Technical Support Analyst (Tier 1) - Polish Native / Spain Homebased
IQVIA
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Full Time
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5 days ago
IQVIA
Provide high-quality phone-based service desk support to end users for IT problems and service requests. Use remote control tools and monitoring systems to identify root causes and resolve technical incidents.
Own the execution and delivery of Agentic AI products from Proof of Concept through to production. Translate business needs into technical requirements and manage the product backlog and acceptance criteria for engineering teams.
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.
Leads the end-to-end execution of COA and eCOA licensing services for global clinical studies, serving as a subject matter expert for clients and internal stakeholders. Manages a delivery team of consultants to ensure compliant, high-quality outcomes and supports commercial growth through proposal development.
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.
The role focuses on maximizing national sales growth for a pharmaceutical project through remote interactions and online meetings with healthcare professionals. Responsibilities include developing tailored communication materials, reporting daily calls, and optimizing resource allocation to drive sales.
Lead complex eCOA programs ensuring successful delivery of scope, timeline, and quality while managing a team of 7-8 project managers. Drive operational excellence through process improvement, SOP development, and high-level stakeholder communication.
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 managing project timelines for investigative sites.
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 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.
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.
Update and maintain reference databases for the German market by classifying products and standardizing data. Collaborate with local offices to resolve data inaccuracies and maintain process documentation.
The Analyst provides operational and strategic support for client engagements focusing on commercial effectiveness and market assessments in the life sciences industry. They are responsible for processing IQVIA data assets to generate actionable insights and supporting the development of client presentations and workshops.
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.
Consultant, Client Engagement Measurement, IQVIA Digital (Remote)
IQVIA
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Full Time
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6 days ago
IQVIA
The role involves executing measurement projects for life sciences clients, focusing on quality control of outputs and insight generation. Responsibilities include developing study design summaries, performing quantitative/qualitative analyses, and creating client deliverables.
Director, Solution Sales, Small Pharma Segment Lead, IQVIA Digital (Remote)
IQVIA
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Full Time
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6 days 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.
Programmeur principal en épidémiologie, données du monde réel (RWE) – FSP, Senior Epidemiological Programmer, Real World Evidence - FSP
IQVIA
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Full Time
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6 days ago
IQVIA
Lead the development of analytic datasets and conduct longitudinal analyses for observational studies in the virology therapeutic area. Collaborate with epidemiologists to define statistical specifications and develop TFLs for protocols and manuscripts.
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.
Clinical Biospecimen Scientist - Single Sponsor Dedicated (home-based in Poland)
IQVIA
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Full Time
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6 days ago
IQVIA
Lead the biospecimen strategy for global clinical trials, overseeing the entire lifecycle of sample collection, analysis, and data transfer. Manage lab setups, develop training materials for clinical sites, and ensure strict data integrity and budget oversight.
Perform site monitoring visits including selection, initiation, and close-out in accordance with GCP and ICH guidelines. Manage study progress by tracking recruitment, regulatory approvals, and ensuring the integrity of site documentation.
Principal - eCOA Consulting Services - Multiple Locations, Hybrid/Home-based
IQVIA
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Full Time
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7 days ago
IQVIA
Lead the end-to-end lifecycle of eCOA implementation services, from opportunity identification and proposal development to study execution. Drive commercial growth and provide senior oversight to delivery teams while acting as a trusted advisor to life sciences clients.
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.
The Inside Sales Representative is responsible for achieving sales forecasts and increasing product adoption within the GI space. This involves managing inbound and outbound sales calls and building strong relationships with targeted physicians and accounts.
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 regulatory standards.
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 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 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 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.
Provide remote technical support to users by troubleshooting issues and implementing practical solutions. Assist with user training on common tools and escalate complex technical problems to senior team members.
Provides strategic medical and scientific oversight for global clinical research programs in Hematology and Oncology. Acts as the primary medical interface between the company, sponsors, and sites to ensure compliant and efficient trial execution.
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.
Lead end-to-end country-level clinical trial delivery from start-up through closeout, ensuring high-quality data and regulatory compliance. Manage site performance, stakeholder engagement, and country-level budgets and vendors.
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.
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 tracked according to project timelines.
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.
The Recall Analyst manages and coordinates product recall projects by communicating issues to healthcare professionals via inbound and outbound calls. They are also responsible for maintaining accurate project documentation and tracking progress in internal databases.
Experienced Clinical Trial Coordinator (m/w/d), Home Office in Germany
IQVIA
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Full Time
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11 days ago
IQVIA
The role involves managing clinical trial documentation, maintaining the Trial Master File, and coordinating communication between research sites and internal departments. Additionally, the coordinator will mentor junior staff and assist with the distribution of clinical trial supplies.
Tech/Systems Support Analyst - Spanish Native/English Fluent (Portugal Homebased)
IQVIA
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Full Time
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11 days 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.
Responsible for the daily validation and maintenance of HCP and HCO data within the OneKey platform to ensure accuracy and consistency. This includes mapping data from various sources, performing quality assurance, and resolving data issues through root cause analysis.
Coordonnateur(trice) principal(e), Mise en place de projets de laboratoire/Senior Laboratory Project Set-Up Coordinator
IQVIA
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Full Time
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11 days ago
IQVIA
The role provides operational support for the design, loading, and validation of laboratory databases within Clinical Trial Management Systems. It involves coordinating project set-ups, maintaining accurate documentation, and ensuring compliance with SOPs and ICH E6 guidelines.
Responsible for generating study strategies and performing data mining and analysis to provide competitive enrollment and site strategies. Collaborates with internal stakeholders and global teams to present recommendations for clinical research opportunities.
Develops and sustains the Quality Management System to ensure products meet regulatory and customer requirements. Leads internal and external audits, including SOC 1 and SOC 2, while driving operational efficiency through continuous improvement methodologies.
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.
Manage site activation activities and serve as the single point of contact for investigative sites and project management teams. Ensure all regulatory and contractual documents are accurately prepared, tracked, and executed according to project timelines.
Healthcare Data Verifier German Speaker - Remote ( 3 months Temp- Spain)
IQVIA
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Full Time
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12 days ago
IQVIA
The role involves the daily maintenance, validation, and quality management of Healthcare Professional and Organization data within German databases. It requires conducting research and analysis to resolve client data inquiries and ensure data integrity.
Director, Solution Sales – Large & Mid Pharma Segment Lead, IQVIA Digital (Remote)
IQVIA
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Full Time
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12 days 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.
Coordinate the operational delivery of patient recruitment and retention services for clinical studies across multiple countries. Manage translations, shipping, regulatory submissions, and study tracking while collaborating with internal stakeholders and external vendors.
Serve as the primary point of contact for a portfolio of small pharmaceutical clients to ensure satisfaction and revenue growth. Drive the adoption of IQVIA's data assets and commercial solutions through consultative selling and cross-functional coordination.
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.
Acts as the Lead Medical Writer responsible for preparing clinical study reports and protocols according to SOPs and client requirements. Manages project timelines, budgets, and provides mentorship to junior staff while maintaining direct client communication.
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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13 days 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.
The role focuses on executing the MIDAS commercial strategy to drive revenue, pipeline generation, and new logo acquisition. It involves managing accounts, driving product upgrades, and collaborating with cross-functional teams to expand market insights solutions.
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.
Lead country-level regulatory start-up activities in Poland, focusing on EU CTR submissions via CTIS and site activation. Manage communication with investigative sites, Ethics Committees, and Competent Authorities to ensure compliant and timely trial start-up.
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.
Associate Director, Governance & Data Management Operations Enablement (Remote)
IQVIA
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Full Time
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17 days ago
IQVIA
The role is responsible for operationalizing data governance and compliance requirements while establishing repeatable operating models and processes across the enterprise. It involves serving as the primary representative for IQVIA Digital in governance forums to balance regulatory rigor with product velocity.
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.
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.
Senior Epidemiologist, HIV Treatment, Retrospective Claims Study Expertise (FSP Sponsor Dedicated)
IQVIA
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Full Time
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17 days 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.
Design, build, and optimize scalable data pipelines and architectures to support AI-driven healthcare products. Collaborate with cross-functional teams to ensure data integrity, security, and performance across complex datasets.
The role focuses on identifying and evaluating high-performing investigative sites for clinical trials across Europe. Key tasks include conducting feasibility activities, managing site outreach, and coordinating CDA collections.
Therapeutic Strategy Lead - Internal Medicine/Immunology (Home-Based)
IQVIA
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Full Time
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18 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.
Registered Dietitian – Clinical Research Support in Argentina (Tucuman)
IQVIA
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Full Time
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18 days ago
IQVIA
Conduct comprehensive nutritional assessments and provide ongoing counseling to participants in international clinical research projects. Collaborate with the research team via telehealth to ensure adherence to study protocols and maintain confidential documentation.
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 role focuses on identifying and selecting investigator sites across Europe through outreach and data collection. Key tasks include distributing feasibility questionnaires, tracking responses, and coordinating Confidentiality Disclosure Agreements.
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.
Lead global shipping oversight for digital health import and export activities in support of global clinical trials. Coordinate with 3PL providers and cross-functional clinical teams to ensure device logistics scope and delivery expectations are met.
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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19 days 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.
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.
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.
Perform site selection, initiation, monitoring, and close-out visits while tracking subject recruitment and regulatory submissions. Ensure study site practices adhere to protocols and applicable regulations while maintaining detailed site management documentation.
Therapeutic Strategy Lead - Internal Medicine/Immunology (Home-Based)
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. Bridge the gap between sales, medical, and operational teams to ensure seamless project execution and business growth.
Associate Director, Program Management – Patient Support Services – Remote
IQVIA
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Full Time
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20 days ago
IQVIA
Oversee patient support programs and manage client relationships to achieve short-term and long-term growth goals. Supervise daily workflows, manage SOP documentation, and present program metrics to the executive team.
Lead and deliver a portfolio of global Remote Research Clinicians projects with full accountability for quality, timelines, and financial outcomes. Act as the primary interface between sponsors, sites, and clinicians while managing project documentation and risk mitigation.
The Senior Technical Project Manager bridges business objectives and engineering execution to deliver scalable, integrated solutions across patient access platforms. They are responsible for defining system architecture, managing technical risks, and enforcing governance standards across complex multi-system environments.
The Senior Medical Director provides strategic scientific expertise to lead clinical development plans and execute group strategies within a specific therapeutic area. They are responsible for proposal development, bid defense meetings, and acting as a consultant throughout the research and development lifecycle.
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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24 days 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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24 days 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.
Attaché de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
IQVIA
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Full Time
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24 days ago
IQVIA
The CRA II is responsible for monitoring Phase I-IV 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.
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.
The role involves managing clinical trial start-up activities, including site identification, feasibility, and regulatory submissions. The specialist acts as the primary contact for investigative sites to ensure compliance with ICH-GCP and local regulations.
Lead the strategic and operational delivery of site activation activities to accelerate patient enrollment across global studies. Manage regulatory submissions, site contracting, and maintain strong sponsor relationships to ensure timely study start-up.
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.
Manage site activation activities and serve as the single point of contact for investigative sites and project management teams. Ensure the accurate preparation, review, and submission of regulatory and contractual documents in compliance with local and international regulations.
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.
Design and conduct epidemiological studies to generate real-world evidence, focusing on oncology and natural history of disease. Lead the development of study protocols, analysis plans, and reports to support regulatory and internal decision-making.
Senior Epidemiologist, Inflammation, External Comparator Expertise (FSP Sponsor Dedicated)
IQVIA
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Full Time
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a month ago
IQVIA
Lead the design and execution of innovative real-world evidence strategies and observational research to inform clinical development and regulatory decisions. Manage the full study lifecycle, including protocol development, data strategy, and stakeholder alignment for a dedicated sponsor.
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.
Define and govern enterprise-wide architecture strategies, standards, and roadmaps with a focus on clinical operations and trial management. Co-design target-state architectures and reference models to reduce technical debt and optimize trial execution using AI and automation.
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.
Associate Director- HCP, Consumer, Identity Operations (Remote)
IQVIA
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Full Time
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a month ago
IQVIA
Leads specialized operational teams managing Identity, Consumer, and HCP data to ensure quality, standardization, and SLA compliance. Partners with product and engineering teams to translate requirements into scalable data pipelines and operational workflows.
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.
Recruit short-term acute care hospitals and IDNs to participate in the IQVIA Hospital Data Exchange Program. Provide technical support and relationship management to ensure high-quality data submission and program engagement.
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 Epidemiologist, Inflammation, IBD (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, including natural history of disease and comparative effectiveness research. Lead the development of study protocols, analysis plans, and regulatory documents to support drug development and safety queries.
Lead and accelerate growth for strategic global Consumer Health clients by owning senior executive relationships and setting multi-year account strategies. Orchestrate cross-functional teams to deliver integrated data, analytics, and technology solutions that drive revenue and enterprise-level partnerships.
Senior Account Manager, Platform Success - IQVIA Digital (REMOTE)
IQVIA
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Full Time
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a month 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.
Senior Epidemiologist, Inflammation, EHR 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, including natural history of disease and comparative effectiveness research. Lead the development of study protocols, analysis plans, and reports to support regulatory and internal decision-making.
Design and conduct epidemiological studies to generate real-world evidence for oncology therapies, focusing on natural history of disease and treatment patterns. Lead the development of study protocols, analysis plans, and regulatory documents to support internal and external decision-making.
Manage end-to-end site start-up activities, including feasibility, identification, and maintenance across multiple clinical trials. Coordinate ethics submissions, budget negotiations, and contract management while acting as the primary contact for investigative sites.
The role provides scientific support for RWE/Epidemiology studies through literature reviews, data cleaning, and the development of scientific deliverables like manuscripts and posters. Additionally, it involves operational oversight of multiple studies, managing trackers, and coordinating cross-functional safety and data requests.
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.
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.
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.
Responsible for statistical programming for Phase I-IV clinical trials, including the creation of ADaM datasets, tables, listings, and figures. The role involves developing generic SAS code, maintaining analysis standards, and preparing electronic submission packages for regulatory agencies like the FDA and EMEA.
Clinical Research Associate 2 or Senior Clinical Research Associate 1 (m/w/d), Single Sponsor
IQVIA
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Full Time
·
a month ago
IQVIA
The role involves performing site selection, initiation, monitoring, and close-out visits while ensuring compliance with GCP and ICH guidelines. Responsibilities also include managing regulatory submissions, recruitment tracking, and collaborating with study site experts and clients.
Associate Director, Product Management - Contracting (CTFS) (Remote)
IQVIA
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Full Time
·
a month 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.
Registered Dietician Clinical Trials Telehealth - Per Diem - Ohio
IQVIA
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Full Time
·
2 months ago
IQVIA
Conduct nutritional assessments via telehealth and develop individualized dietetic care plans for patients with rare and complex conditions. Provide ongoing dietary counseling and monitor patient progress and adherence within clinical research studies.
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-scale 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
·
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
·
2 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 - North Carolina
IQVIA
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Full Time
·
2 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 - Nevada
IQVIA
·
Full Time
·
2 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 - Missouri
IQVIA
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Full Time
·
2 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 - Washington
IQVIA
·
Full Time
·
2 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
·
Full Time
·
2 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
·
2 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.
Senior Clinical Research Associate, Early Clinical Development
IQVIA
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Full Time
·
2 months ago
IQVIA
The Senior CRA is responsible for monitoring and managing clinical sites to ensure strict adherence to study protocols, regulatory requirements, and sponsor expectations. They will conduct various site visits, facilitate subject recruitment, and maintain essential study documentation to ensure high-quality clinical research data.
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
·
2 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
·
2 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
·
2 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.
Study Start-Up Clinical Research Associate, Sponsor Dedicated
IQVIA
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Full Time
·
2 months ago
IQVIA
The Study Start-Up CRA is responsible for managing site selection, study-specific start-up activities, and ensuring deliverables are met for Phase I-IV trials. They act as the primary contact for trial sites, facilitating document collection, regulatory submissions, and site greenlight processes.
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
·
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 Asset Commercialization Partner acts as a trusted advisor to emerging biopharma clients, developing integrated commercialization strategies and launch plans. They are responsible for leading client engagements, identifying new business opportunities, and mentoring internal teams to deliver high-quality solutions.
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
·
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
·
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.
Lead data management for complex, global clinical trials from study setup to database lock. Serve as the main client contact for all data management deliverables.
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.
The role involves editing and performing Quality Control (QC) on documents created for clinical trials, Post-Marketing Surveillance (PMS), and clinical research, adhering strictly to internal or client Standard Operating Procedures (SOPs). Responsibilities also include meeting deadlines and contributing to high-quality document creation through teamwork.
The Clinical Data Management Lead will be responsible for leading end-to-end data management delivery for complex, global clinical trials, serving as the main client contact for all data management deliverables. This includes overseeing SAE, PK, and external data reconciliation, managing project logistics, mentoring staff, and ensuring compliance with regulations and SOPs.
Medical Biller/Claims Processing - Patient Support Representative (Remote; 10am-7pm EST)
IQVIA
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Full Time
·
3 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
·
3 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
·
3 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
·
3 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.
The specialist will serve as the Single Point of Contact for investigative sites regarding Site Activation activities, ensuring adherence to regulations, SOPs, and project timelines. Key tasks include preparing and reviewing regulatory documents, maintaining internal systems, and tracking the progress of document approvals for individual sites.
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
·
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 specialist will review, assess, and process safety data from various sources across service lines, distributing reports internally and externally according to regulations and SOPs. Main duties involve performing pharmacovigilance activities such as collecting Adverse Events, database entry, coding, writing narratives, and literature review.
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.
Flex Nurse Educator - Fresno, CA (Must have/obtain CA license)
IQVIA
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Full Time
·
4 months ago
IQVIA
The Flex Nurse Educator delivers essential remote educational support and medication training to patients with chronic diseases using various virtual channels. This role also requires providing in-person education exclusively during territory vacancy coverage to maintain seamless program continuity and compliance.
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
·
6 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.
IT-Systemadministrator – Microsoft Infrastruktur (m/w/d) - full remote
IQVIA
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Full Time
·
6 months ago
IQVIA
As a System Administrator, you will ensure smooth daily operations and support cross-location topics. Your tasks will include managing migrations, addressing standards and certifications, and proactively handling new topics.
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
·
7 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
·
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
·
8 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.
