The Senior Data Team Lead oversees end-to-end data management delivery for global clinical trials, ensuring quality, accuracy, and regulatory compliance. They serve as the primary client contact while managing timelines, budgets, and cross-functional teams.
IQVIA
252 Remote Job Openings at IQVIA
Global Clinical Project Manager - Vendor Management Expert (home-based in Poland)
IQVIA
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Full Time
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a day ago
IQVIA
The Global Clinical Project Manager is responsible for overseeing vendor deliverables across the study lifecycle to ensure quality and efficiency. Key tasks include managing vendor performance, supporting site activation, and coordinating study close-out activities.
The Medical Director provides medical and scientific expertise for clinical trials, including medical monitoring and support for investigative sites. They also contribute to business development by providing strategic advice and participating in client proposals and bid defense meetings.
The role involves administering clinical assessments to trial participants and evaluating the quality of assessments performed by other raters to ensure data reliability. You will provide feedback on methodology and scoring while maintaining accurate documentation for clinical trial activities.
The Medical Director serves as a medical monitor for clinical trials in neurology, providing scientific advice and support to project teams and investigative sites. They also contribute to medical strategy by reviewing protocols, supporting client proposals, and ensuring regulatory and scientific soundness.
The role involves administering clinical assessments to trial participants and evaluating the quality of assessments performed by other raters to ensure data standardization. You will provide feedback on scoring techniques, manage documentation, and conduct remote interactions with participants and raters.
The Therapeutic Strategy Director leads cross-functional teams to design innovative, data-driven solutions for internal medicine programs to secure new business. They act as a strategic expert throughout the proposal and delivery lifecycle, ensuring client satisfaction and project success.
The Director of Operations is responsible for driving the growth, scalability, and operational consistency of the Remote Research Clinicians business. This role provides strategic leadership across client engagement, technology-enabled operations, and quality oversight to ensure delivery excellence.
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 quality, managing budgets, and implementing process improvements.
The Associate Business Development Director is responsible for prospecting, qualifying, and closing new business opportunities within medical specialty societies. This role involves developing comprehensive sales plans, managing the full sales cycle, and serving as a liaison between customers and internal technical teams.
Therapeutic Strategy Director - Cardiovascular, Renal, Metabolic
IQVIA
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Full Time
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2 days ago
IQVIA
The Therapeutic Strategy Director leads cross-functional teams to design innovative, data-driven solutions for CVRM programs to secure new business. They act as a strategic expert throughout the project lifecycle, ensuring client-centric proposals and effective delivery strategies.
Process and assess safety data and adverse events in accordance with regulatory requirements and internal SOPs. Collaborate with functional team members and healthcare professionals to ensure accurate reporting and project compliance.
The Senior Director is responsible for executing patient services strategy and overseeing the performance of call center programs for pharmaceutical and medical device clients. They will lead leadership teams, manage client relationships, and ensure operational excellence to meet revenue and profit targets.
The Talent Acquisition Specialist will source, select, and hire qualified candidates for vacant positions while supporting staffing programs within the EMEA region. They will also collaborate with management to establish staffing objectives and ensure compliance with local hiring guidelines.
The Regulatory and Start Up Specialist serves as the single point of contact for site activation activities, ensuring adherence to regulatory standards and project timelines. They are responsible for preparing and reviewing site regulatory documents, maintaining internal databases, and coordinating with project teams to ensure successful site activation.
Senior Director, Integrated Platforms & Information Management, MedTech
IQVIA
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Full Time
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2 days ago
IQVIA
The Senior Director leads the global MedTech Information Management strategy by integrating data stewardship, analytics, and core solutions into a scalable portfolio. They are responsible for driving revenue growth, managing investment priorities, and fostering cross-functional collaboration to deliver market-relevant solutions.
Quality Assurance Business Analyst - Patient Access & Support Services (Remote)
IQVIA
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Full Time
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3 days ago
IQVIA
The Quality Assurance Analyst evaluates patient services interactions to ensure compliance with regulatory and contractual standards. They also document findings, identify quality trends, and support operational improvements through data-driven insights.
The Clinical Lead is responsible for the end-to-end clinical delivery of assigned studies, ensuring compliance with regulatory requirements and internal SOPs. They lead clinical teams, manage project risks, oversee clinical quality, and collaborate with stakeholders to meet recruitment and financial targets.
The Medical Director provides strategic scientific leadership across client accounts and leads, mentors, and develops a team of scientific professionals. They are responsible for ensuring operational excellence, driving business growth, and maintaining the scientific integrity of high-impact client deliverables.
The Clinical Project Lead will serve as the primary country-level leader for clinical trial delivery, overseeing operations from start-up through closeout. They are responsible for ensuring high-quality data, managing site performance, and maintaining compliance with regulatory standards and ICH-GCP guidelines.
Lead the startup strategy and execution for Remote Research Clinician services across a portfolio of clinical studies. Partner with sponsors and cross-functional teams to design and implement patient-centric, hybrid, and decentralized trial models.
Campaign Operations & Audience Selection Specialist - English/Dutch Speaker - Home Based
IQVIA
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Full Time
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3 days ago
IQVIA
You will support the delivery of healthcare marketing campaigns by managing email, landing pages, and audience selection within a highly regulated environment. Additionally, you will focus on standardizing and automating processes to improve operational efficiency and ensure high-quality documentation.
The Nurse Educator facilitates connections between patients and approved educational resources while delivering disease-specific training on prescribed therapies. They promote behavioral change to improve treatment adherence and encourage effective communication between patients and their healthcare providers.
The LLM Engineer will develop, fine-tune, and optimize Large Language Models and agentic AI solutions using proprietary healthcare datasets. They will also manage the full AI development lifecycle, including data preparation, model training, deployment, and integration into business workflows.
Lead end-to-end data management for complex, global clinical trials from study setup to database lock. Serve as the primary client contact while managing timelines, budgets, and cross-functional team performance.
Lead end-to-end data management for complex, global clinical trials from study setup through database lock. Serve as the primary client contact while managing timelines, budgets, and cross-functional team performance.
Lead end-to-end data management for complex, global clinical trials from study setup through database lock. Serve as the primary client contact while managing timelines, budgets, and cross-functional team performance.
Lead end-to-end data management for complex, global clinical trials from study setup to database lock. Serve as the primary client contact while managing timelines, budgets, and cross-functional team performance.
The Finance Manager will support monthly corporate consolidation processes and internal financial reporting while ensuring compliance with US GAAP and SOX requirements. They will also partner with cross-functional teams to drive process improvements, automation, and support strategic transactions like mergers and acquisitions.
Director, Client Services - Medical & Scientific Communications
IQVIA
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Full Time
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4 days ago
IQVIA
The Director will lead strategic client relationships and oversee delivery excellence across complex medical and scientific communication accounts. They are responsible for driving organic growth, managing financial performance, and developing high-performing teams to meet client objectives.
The Scientific Advisor is responsible for developing high-quality scientific content and partnering with stakeholders to meet client strategy and branding objectives. They also collaborate with Client Services and Marketing teams to ensure project timelines are met and provide scientific expertise for clinical studies and product narratives.
The Data Acquisition Specialist manages the definition, setup, and ingestion of external data streams for clinical trials. They liaise with stakeholders and data providers to ensure data transfer agreements are accurate and compliant with regulatory standards.
Design and develop software solutions that integrate medical devices into the ClinSpark platform to enable seamless data flow. Contribute to both front-end and back-end development while ensuring high software quality through testing and code reviews.
The moderator will conduct one-to-one qualitative interviews with patients and healthcare professionals to capture authentic patient experiences and treatment journeys. They will also collaborate with research teams to refine interview guides and ensure high-quality data collection for clinical and commercial decision-making.
The role involves providing regulatory oversight and strategic guidance for clinical trial submissions across global programs. Responsibilities include authoring regulatory documentation, managing submission processes, and ensuring compliance with internal SOPs and regulatory requirements.
Deliver high-quality diabetic care and education to patients across various settings, including remote consultations. Collaborate with multidisciplinary teams to support holistic patient care and participate in health initiatives.
The role involves reviewing patient-level clinical and safety data to ensure medical accuracy and consistency while generating queries for case closure. Additionally, the scientist will contribute to study start-up activities and collaborate with study physicians to support high-level medical evaluation.
The Associate Director acts as the primary medical and scientific point of contact for final content approval, ensuring promotional and non-promotional materials align with FDA, PhRMA, and FTC requirements. They also collaborate with cross-functional teams to provide strategic compliance advice and support business development efforts.
Registered Dietitian β Clinical Research Support (New Zealand)
IQVIA
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Full Time
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4 days ago
IQVIA
Conduct comprehensive nutritional assessments and provide ongoing counseling to study participants via telehealth. Collaborate with the clinical research team to ensure adherence to study protocols and maintain accurate documentation.
The role involves ensuring the accuracy and completeness of clinical and safety data through ongoing review and medical assessment. The scientist will also facilitate safety data meetings, contribute to study start-up activities, and collaborate with study physicians to manage medical cases.
The Project Manager will serve as the primary point of contact for live eCOA studies, leading client meetings and managing system changes. They are responsible for maintaining project scope, tracking risks, managing budgets, and ensuring accurate documentation throughout the study lifecycle.
You will be responsible for processing and submitting safety reports to regulatory authorities in accordance with SOPs and project requirements. Additionally, you will liaise with functional team members and healthcare professionals to address project-related issues and ensure compliance with quality standards.
Bi-lingual Pharmacy Tech Support/Call Center Rep (Work from Home)
IQVIA
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Full Time
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5 days ago
IQVIA
The representative will serve as the primary contact for patients and medical professionals to assist with program eligibility, card activation, and benefit explanations. They are responsible for documenting resolutions and troubleshooting submission rejections via phone, email, or fax.
Epidemiologist, Virology, Real World Evidence (FSP Sponsor Dedicated)
IQVIA
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Full Time
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5 days ago
IQVIA
Design and conduct epidemiological studies to generate real-world evidence while ensuring adherence to time, budget, and quality standards. Collaborate with sponsors to analyze observational data and communicate findings to support internal and external decision-making processes.
The associate manager will generate study strategies and collaborate with IQVIA teams to provide competitive edges in winning new business. They are responsible for performing data mining, formulating recommendations, and presenting analysis to internal and external stakeholders.
The Nurse Educator facilitates patient connections to educational resources and provides personalized training on chronic disease management and prescribed therapies. They promote treatment adherence and encourage effective communication between patients and their healthcare providers.
The Contract Negotiation Specialist is responsible for independently drafting, reviewing, and negotiating clinical trial agreements to support study start-up activities. They act as a primary point of contact for sites and internal teams while ensuring all contracts comply with regulatory requirements and project timelines.
Associate Project Services Manager - (Clinical Trials and Laboratories)
IQVIA
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Full Time
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5 days ago
IQVIA
Manage all laboratory aspects of clinical trial projects from award through closeout, serving as the primary point of contact for sponsors. Lead study set-up, monitor project timelines and budgets, and coordinate cross-functional resources to ensure high-quality execution.
Perform site selection, initiation, monitoring, and close-out visits while ensuring compliance with regulatory requirements. Manage study progress by tracking regulatory submissions, recruitment, and data query resolutions.
The Principal Biostatistician serves as the statistical lead for late-phase clinical trials, providing strategic guidance and scientific oversight. They are responsible for authoring statistical analysis plans, performing complex analyses, and collaborating with cross-functional teams to ensure regulatory compliance.
Lead the full scope of biostatistics conduct for therapeutic programs, including defining statistical strategy and ensuring appropriate methodologies for clinical trials. Collaborate with cross-functional teams and regulatory authorities to deliver high-quality interim and final results for clinical development plans.
Business Development Representative, Quality & Regulatory Affairs Technology
IQVIA
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Full Time
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5 days ago
IQVIA
The Business Development Representative will drive growth for the QARA Center of Excellence by identifying new business opportunities through strategic prospecting and outbound outreach. They will work closely with Account Executives to qualify leads, build a strong sales pipeline, and manage data within Salesforce.com.
Develop and maintain C++ applications and database processes for payment and billing management in the healthcare sector. Implement legal requirements, automate testing, and refactor existing processes using modern technologies and agile methods.
Conduct standardized remote clinical interviews and psychiatric assessments for participants in a PTSD clinical research study. Ensure protocol compliance, data quality, and the accurate scoring of study-specific rating scales.
Conduct standardized remote clinical interviews and psychiatric assessments for participants in a PTSD clinical research study. Ensure protocol compliance, data quality, and consistency while administering specific rating scales.
The specialist is responsible for the definition, set-up, and ingestion of external data streams in alignment with clinical trial protocols. This includes developing Data Transfer Agreements and performing UAT to ensure data accuracy and consistency.
Acts as the primary point of contact for clients regarding live eCOA studies and manages project scope, plans, and schedules. Leads client update meetings, manages system change efforts, and handles project documentation and budgeting.
The Project Management Analyst supports clinical trial delivery by managing project schedules, finances, and risk mitigation strategies. They are responsible for maintaining performance dashboards, ensuring eTMF compliance, and coordinating communication between project leaders and customers.
The specialist serves as the single point of contact for site activation activities, ensuring adherence to regulations and project timelines. Responsibilities include preparing regulatory documents, tracking approvals, and performing quality control on site deliverables.
Manage Site Enrollment and Engagement Lead (SEEL) teams to optimize clinical trial enrollment and ensure compliance with regulations. Provide operational delivery of team strategies, conduct performance reviews, and deliver regular project updates to stakeholders.
Country Activation and Submission Representative (Home-Based, Poland) - IQVIA Biotech
IQVIA
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Full Time
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6 days ago
IQVIA
Manage country-level regulatory and site activation activities for clinical studies in Poland, including EU CTR submissions and amendments. Coordinate with investigative sites and regulatory authorities to ensure compliance and timely study start-up and maintenance.
The coordinator performs country-level site activation activities, including feasibility and maintenance for investigative sites. They are responsible for preparing, tracking, and reviewing essential regulatory and ethics documents to ensure clinical trial compliance.
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 from collection and analysis to data transfer. Manage lab setups, develop training materials for clinical sites, and ensure accurate sample disposition and budget oversight.
The Medical Director serves as the medical expert for clinical trials focusing on neurological diseases, primarily handling medical monitoring and scientific advisory. They are responsible for protocol-related support, analyzing adverse events, and contributing to the medical strategy of client proposals.
Associate Manager / Manager, Project Services - Laboratories (Remote - East Coast)
IQVIA
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Full Time
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8 days ago
IQVIA
Manage all laboratory aspects of clinical trial projects from award through closeout, serving as the primary point of contact for sponsors. Lead project planning, risk management, and cross-functional coordination to ensure high-quality execution and protocol compliance.
Associate Manager / Manager, Project Services - Laboratories (Remote - West Coast)
IQVIA
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Full Time
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8 days ago
IQVIA
Manage all laboratory aspects of clinical trial projects from award through closeout, serving as the primary point of contact for sponsors. Lead project planning, risk management, and cross-functional coordination to ensure high-quality execution and protocol compliance.
Manage an assigned territory by engaging healthcare professionals through inbound and outbound calls to increase awareness and utilization of Thyrogen. Provide product education, support patient access initiatives, and maintain accurate customer records in CRM platforms.
The Clinical Specialist ensures the integrity of clinical trial data by reviewing assessment scales and providing guidance to raters. Responsibilities include conducting live interactions to improve scoring techniques and supporting rater performance through functional assessments.
Job Posting Title Clinical Trial Psych Rater - Italian Speaking
IQVIA
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Full Time
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9 days ago
IQVIA
The role involves reviewing psychiatric rating scales to ensure standardized assessment practices and data integrity. The specialist will provide guidance to raters through live discussions and functional assessments like mock interviews.
Site Enablement Lead (Trilingual: Portuguese, Spanish and English)
IQVIA
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Full Time
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10 days ago
IQVIA
The Site Enablement Lead supports clinical study execution by identifying and training qualified research staff to accelerate study deliverables. They also optimize patient referral flows using the Referral Hub platform and manage site-level service agreements and staffing.
Lead the design and delivery of scalable AI solutions for pharmaceutical and life sciences organizations to accelerate drug development. Act as a trusted advisor to stakeholders, translating complex scientific challenges into technical architectures using LLMs and knowledge graphs.
The specialist serves as the single point of contact for site activation activities, ensuring adherence to SOPs and regulatory guidelines. They are responsible for preparing regulatory documents, tracking approvals, and maintaining internal project databases.
The specialist serves as the single point of contact for site activation activities, ensuring adherence to SOPs and regulatory guidelines. They are responsible for preparing regulatory documents, tracking approvals, and maintaining internal project databases.
Associate Principal, Indirect Treatment Comparison (ITC), Evidence Synthesis
IQVIA
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Full Time
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10 days ago
IQVIA
Lead the implementation of evidence synthesis projects to support HTA and regulatory submissions from pre-award to final delivery. Manage project teams, oversee financial and administrative requirements, and drive business development through proposals and bid defenses.
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.
Coordinate site activation activities for clinical research studies to ensure compliance with regulations and project timelines. Maintain regulatory documentation and track approvals for ethics, contracts, and informed consent forms.
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.
The role focuses on identifying and closing new business opportunities with regional and national healthcare payer clients to drive revenue growth. Responsibilities include managing the full sales cycle, developing strategic account plans, and aligning IQVIA's data and technology solutions with client needs.
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 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 overseeing data reconciliation, budgets, and the mentoring of junior staff.
Client Services Representative, Interactive Response Technology (IRT) (2nd Shift)
IQVIA
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Full Time
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11 days ago
IQVIA
Provide proactive Helpdesk support to investigator sites and IVR companies, handling escalation calls and resolving technical issues via the Admin console. Support the IRT/Logistics project management team with administrative tasks, site data maintenance, and the creation of site documentation.
Provide strategic medical and scientific expertise in hematology-oncology to support proposal development, protocol design, and client engagements. Act as a subject matter expert throughout the research and development lifecycle to guide project teams and sponsors.
The role focuses on supporting client data onboarding and intake processes by partnering with vendors and internal teams. Key duties include communicating file requirements, tracking acquisition timelines, and resolving data-related issues to support value-based care strategies.
Drive new and expansion revenue for digital marketing offerings targeting hospital and health system clients across the West Coast. Partner with Account Directors to identify growth opportunities and deliver data-driven solutions that improve service line performance.
Lead complex enterprise client implementations from kickoff through deployment, serving as a trusted advisor to senior stakeholders. Coordinate with cross-functional teams to translate business requirements into technical specifications and ensure successful project execution.
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.
Country Activation and Submissions Representative_(Home-Based, Portugal) - IQVIA Biotech
IQVIA
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Full Time
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12 days ago
IQVIA
Manage country-level regulatory and site activation activities, including EU CTR submissions and the maintenance of Essential Document Packages. Act as the primary contact for investigative sites and coordinate approvals from regulatory authorities and ethics committees.
Associate Decentralized Clinical Trial Lead / Decentralized Clinical Trial Lead
IQVIA
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Full Time
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13 days ago
IQVIA
Accountable for the strategic development and delivery of decentralized and hybrid clinical trials while optimizing speed, quality, and cost. This role involves managing customer relationships, overseeing project financials, and collaborating across functional teams to ensure regulatory compliance.
The role involves identifying and selecting investigator sites across Europe through outreach and data collection. Key tasks include managing feasibility questionnaires, tracking responses, and coordinating Confidentiality Disclosure Agreements.
Support the planning and delivery of live events by managing reports, data, and financial reconciliations. Collaborate with Event Project Managers to ensure projects are delivered on time, within scope, and according to budget.
The Centralized Monitoring Lead will oversee the Centralized Monitoring team and partner with project and clinical leads to ensure project objectives are met. Responsibilities include managing clinical deliverables, project resources, and developing monitoring strategies.
Trainee Clinical Research Associate (m/w/d), Home-Office throughout Germany
IQVIA
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Full Time
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16 days ago
IQVIA
The role involves performing site selection, initiation, monitoring, and close-out visits for a specific pharma client. Responsibilities include managing regulatory submissions, tracking recruitment, and ensuring the quality and integrity of site practices.
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 site activation activities and serve as the single point of contact for investigative sites and project management teams. Ensure adherence to SOPs and regulatory guidelines while tracking the approval of ethics and contractual documents.
Senior National Account Manager β Pharmaceutical/MedTech Market Access β Remote
IQVIA
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Full Time
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17 days ago
IQVIA
The National Accounts Director manages payer account management and targeted market access accounts to ensure product coverage and formulary status. They lead teams of National Account Directors, providing strategic direction and monitoring project performance for pharmaceutical and biotech clients.
Consultant principal, statisticien / Senior Consultant, Statistician, Indirect Treatment Comparison (ITC), Evidence Synthesis
IQVIA
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Full Time
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17 days ago
IQVIA
Lead the implementation of evidence synthesis projects to support HTA and regulatory submissions from pre-award to final delivery. Manage project teams, oversee operational and financial requirements, and drive business development through proposal creation and lead qualification.
Senior Consultant, Evidence Synthesis, Indirect Treatment Comparison (ITC)
IQVIA
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Full Time
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17 days ago
IQVIA
Lead the design and implementation of methodologically rigorous evidence synthesis and HTA-compliant studies. Manage project delivery, oversee junior staff, and develop analyses using R to support client business objectives.
Develop automation tools, coding scripts, and efficiency software to support the Evidence Synthesis practice and Centre of Excellence. Contribute to complex statistical projects and disseminate research findings through peer-reviewed journals and scientific conferences.
The role involves reviewing, assessing, and processing safety data and adverse events from various sources. Responsibilities include database entry, coding, writing narratives, and ensuring compliance with SOPs and regulations.
Coordinate and perform remote clinical activities to collect and report patient data in compliance with study protocols and GCP. Manage virtual patient recruitment, enrollment, and informed consent processes while ensuring participant safety.
Lead the development of scientific and promotional medical communications, including manuscripts, posters, and slide decks. Partner with clients to create strategic narratives and ensure all content is scientifically accurate and compliant.
The Scientific Advisor, Director leads biomarker strategies for translational and clinical studies and serves as the scientific lead for protein biomarker programs. This role involves engaging clients, translating complex technical concepts into practical study plans, and supporting business development efforts.
The Scheduler will manage patient onboarding and coordination within the Patient Support Programme, including processing referrals and creating patient records. They will also conduct welcome calls, allocate patients to nurses, and handle telephone queries.
The role involves managing clinical trial start-up activities and site activation in France, focusing on EU CTR package preparations and document collection. The specialist acts as the primary contact for investigative sites to ensure compliance with SOPs and regulatory timelines.
Manage start-up contracting activities, including the development of investigator grant estimates and proposal text for biotech sponsors. Ensure overall contracting efficiency and adherence to project timelines while maintaining internal systems like CTMS.
Manage Medical Information staff and support operational decisions as directed by senior management. Collaborate with stakeholders to achieve local and global deliverables and metrics.
Tech Systems/Support Analyst - Hungarian Native (Portugal Homebased)
IQVIA
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Full Time
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19 days ago
IQVIA
The Tech/System Analyst provides first-level support to Clinical Trials personnel via phone, email, and chat. They ensure timely resolution of technical and operational inquiries.
The Attorney 1 will prepare SEC filings and provide counsel on compliance, governance, and capital markets transactions. They will also manage legal entity reorganizations and coordinate sustainability reporting requirements.
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.
Provide advanced technical expertise to develop process methodology and integrated programming solutions for complex clinical studies. Lead technical teams in creating statistical tables, figures, listings, and analysis datasets while coordinating with internal and external clients.
Manage start-up contracting activities, including developing investigator grant estimates and maintaining contract templates for biotech sponsors. Ensure compliance with regulatory requirements and project timelines while collaborating with stakeholders and RSU regions.
Serve as the primary point of contact for 20-30 small pharmaceutical accounts to drive client satisfaction and revenue growth. Manage day-to-day interactions, commercial administration, and the adoption of IQVIA's data assets and commercial offerings.
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.
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.
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.
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.
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.
AttachΓ© de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
IQVIA
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Full Time
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22 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.
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.
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 associΓ©(e), Services de projets en laboratoire (tΓ©lΓ©travail) / Associate Laboratory Project Services Manager (Remote)
IQVIA
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Full Time
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24 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.
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 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 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. 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. Responsibilities include conducting live feedback sessions, evaluating scoring techniques, and supporting rater performance through mock interviews.
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.
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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25 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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25 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.
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.
Senior Epidemiologist, Immunology, RWE (FSP Sponsor Dedicated)
IQVIA
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Full Time
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a month ago
IQVIA
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.
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.
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.
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IQVIA
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Full Time
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a month ago
IQVIA
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.
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
·
a month 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
·
a month 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.
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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a month 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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a month 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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a month 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.
Senior Clinical Research Associate - Sponsor dedicated - Netherlands - Home based (m/w/d)
IQVIA
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Full Time
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a month 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.
Clinical Research Associate II - Sponsor dedicated - Netherlands - Home based (m/w/d)
IQVIA
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Full Time
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a month 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.
Clinical Research Associate I - Sponsor dedicated - Netherlands - Home based (m/w/d)
IQVIA
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Full Time
·
a month 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.
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.
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.
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.
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.
Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)
IQVIA
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Full Time
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a month 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 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.
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.
Epidemiologist, Internal Medicine, Inflammation & Immunology (FSP Sponsor Dedicated)
IQVIA
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Full Time
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a month 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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a month 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.
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.
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.
Director, Solution Sales, Small Pharma Segment Lead, IQVIA Digital (Remote)
IQVIA
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Full Time
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2 months 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.
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, 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 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 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 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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2 months 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.
Director, Solution Sales β Large & Mid Pharma Segment Lead, IQVIA Digital (Remote)
IQVIA
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Full Time
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2 months 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.
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.
Senior Epidemiologist, HIV Treatment, Retrospective Claims Study Expertise (FSP Sponsor Dedicated)
IQVIA
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Full Time
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2 months 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.
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.
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.
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.
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.
AttachΓ© de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology
IQVIA
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Full Time
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2 months 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.
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.
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.
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.
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.
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.
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.
Data Analyst (SAS / SQL Programming) - German Speaker (Spain remote)
IQVIA
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Full Time
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3 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.
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 - 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 - 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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4 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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4 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.
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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4 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.
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.
Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - Florida
IQVIA
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Full Time
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4 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.
Registered Dietitian β Clinical Research Support (South Korea)
IQVIA
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Full Time
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4 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.
γ‘γγ£γ«γ«γ©γ€γΏγΌοΌFSO Medical Writer/ IQVIA ServicesοΌ
IQVIA
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Full Time
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4 months ago
IQVIA
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.
γ·γγ’γ‘γγ£γ«γ«γ©γ€γΏγΌοΌSr. Medical Writer/ IQVIA ServicesοΌ
IQVIA
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Full Time
·
4 months ago
IQVIA
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 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.
Spanish Bilingual Registered Dietician Clinical Trials Telehealth - Per Diem - Indianapolis
IQVIA
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Full Time
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5 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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5 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.
Associate Director Senior Study Lead - Single Sponsor Dedicated
IQVIA
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Full Time
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5 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.
Registered Dietitian β Clinical Research Support (Bulgaria)
IQVIA
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Full Time
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6 months ago
IQVIA
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.
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.
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
·
9 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 Sponsorβs 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 Devicesβ 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.