The Project Manager will act as the primary point of contact for eCOA studies, managing project scope, timelines, and budgets. They are responsible for leading client meetings, overseeing system changes, and ensuring compliance with operational standards.
You will design and develop software solutions using .NET and Java to support healthcare business processes. Additionally, you will be responsible for maintaining existing software, improving performance, and contributing to architectural decisions.
The Business Development Representative will drive growth for the QARA Center of Excellence by identifying and qualifying new business opportunities through strategic prospecting and outbound outreach. They will work closely with Account Executives to build a strong sales pipeline and manage data within Salesforce.com.
The Virtual Customer Engagement Specialist is responsible for promoting pharmaceutical products to specialty healthcare providers via phone. They must achieve sales forecasts while providing accurate product information and maintaining high levels of customer engagement.
The Pharmacovigilance Specialist is responsible for processing, assessing, and distributing safety data in compliance with regulations and SOPs. They will also perform pharmacovigilance activities such as tracking adverse events, coding products, and writing narratives while liaising with healthcare professionals.
The representative will conduct virtual sales discussions with physicians to provide education, identify referral networks, and promote Boston Scientific therapies. They are responsible for maintaining HCP profiles, managing sales activities in compliance with company policies, and providing regular business updates to leadership.
The role involves managing virtual sales discussions with physicians to educate them on Boston Scientific therapies and identify key referral networks. The incumbent will maintain HCP profiles, provide business updates to leadership, and ensure all sales activities comply with integrity and T&E guidelines.
The Inside Sales Representative is responsible for achieving sales forecasts and driving product adoption within assigned territories. They will coordinate sales strategies with teammates and provide accurate product information to healthcare professionals via phone.
Lead and develop the E-MSL team to execute digital scientific engagement strategies and support connections between medical areas and healthcare professionals. Monitor performance indicators, ensure alignment with medical strategies, and drive the adoption of innovative digital tools.
Lead and manage the day-to-day activities of the Client Delivery Team to ensure high-quality project execution and service delivery. Build strong client relationships while ensuring all studies are planned and executed in accordance with regulatory guidelines and internal policies.
The Site Activation Specialist serves as the primary point of contact for investigative sites and project teams to manage clinical research site activation activities. Responsibilities include preparing and negotiating site contracts and budgets, ensuring regulatory compliance, and maintaining project timelines and documentation.
The Regional Specialist serves as a liaison between clinical teams and investigator sites to support the execution of remote and decentralized trial visits. Responsibilities include managing visit logistics, ensuring documentation compliance, and providing operational support to research clinicians.
The Field Nurse Educator provides educational training to patients regarding specific disease states and prescribed medications to improve treatment compliance. They coordinate patient resources and facilitate dialogue between patients and healthcare providers while maintaining strict adherence to program guidelines.
The role involves supporting start-up contracting activities, including developing grant estimates and maintaining contract templates for clinical trials. You will collaborate with sponsors and internal stakeholders to ensure compliance with regulatory requirements and project timelines.
The Local Trial Manager acts as the primary country-level contact for clinical trials, overseeing project progress, site recruitment, and budget management. They ensure study compliance with regulatory requirements, manage vendor contracts, and maintain essential trial documentation in systems like CTMS.
The Senior Global Trial Manager will lead late-phase clinical trials by overseeing study timelines, budgets, and quality standards. They will also manage cross-functional collaboration, vendor selection, and the development of essential clinical documentation and regulatory submissions.
The Clinical Specialist administers standardized stroke assessments and ensures data quality for clinical trials. They also review assessments conducted by other raters to maintain protocol compliance and provide feedback on scoring methodology.
The Clinical Specialist supports stroke clinical trials by administering standardized assessments and ensuring data quality. They also review assessments conducted by other raters to maintain protocol compliance and provide feedback on scoring techniques.
The PV Safety Specialist is responsible for managing the collection, reporting, and oversight of safety information in compliance with global and local regulatory requirements. They also support the Local Pharmacovigilance Officer in maintaining safety risk management and ensuring inspection readiness across the affiliate.
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 all assigned tasks.
The role involves administering clinical assessments to trial participants and evaluating the quality of assessments performed by other raters to ensure data reliability. The consultant will also provide feedback on methodology and scoring while maintaining accurate documentation for all assigned tasks.
Lead and manage the strategic, operational, and financial delivery of global site activation activities including site identification, regulatory submissions, and contracting. Collaborate with internal and external stakeholders to ensure efficient study start-up and support business development activities.
The Clinical Specialist reviews clinical trial data and assessment scales to ensure standardized practices and data integrity. They also provide guidance to raters through live interactions, feedback, and performance assessments.
The specialist will serve as the single point of contact for site activation activities, ensuring adherence to regulatory requirements and project timelines. They are responsible for preparing and reviewing site regulatory documents and maintaining internal systems with project-specific information.
The Clinical Specialist is responsible for reviewing clinical trial data and assessment scales to ensure standardized practices and data integrity. They provide guidance to raters through live discussions, feedback, and functional assessments to maintain high-quality research standards.
The Clinical Specialist is responsible for reviewing clinical trial data and assessment quality to ensure standardized practices. They provide guidance to raters through live discussions and support performance through functional assessments.
The Clinical Specialist is responsible for reviewing clinical trial data and assessment scales to ensure standardized practices and data integrity. They provide guidance to raters through live discussions, feedback, and functional assessments like mock interviews.
The Clinical Specialist reviews clinical trial data and assessment scales to ensure standardized practices and data integrity. They also conduct live interactions with raters to provide guidance on methodology, scoring, and performance improvement.
The Site Enrollment and Engagement Lead will partner with clinical research sites to develop and implement strategies for patient recruitment, retention, and study delivery. They will also provide essential training to healthcare professionals and site staff regarding clinical trial protocols and procedures.
Design and conduct epidemiological studies to generate real-world evidence, including natural history of disease and treatment pattern assessments. Lead the development of study protocols, analysis plans, and reports while managing cross-functional collaborations in a matrix environment.
The Project Manager will serve as the primary point of contact for eCOA studies, managing project scope, timelines, and budgets. They will lead client meetings, oversee system changes, and ensure compliance with operational standards.
The Associate Director leads complex eCOA programs by managing project scope, timelines, and quality while overseeing a team of project managers. They are responsible for driving operational excellence, mentoring staff, and partnering with stakeholders to ensure successful project delivery.
You will be responsible for designing and implementing database applications and automated processes using MS SQL Server. Additionally, you will maintain and evolve Java-based web applications while supporting quality assurance through test-driven development.
The Site Activation Specialist coordinates and executes site start-up activities for clinical research studies in compliance with regulations and project timelines. They serve as the primary point of contact for investigative sites, ensuring the accurate preparation and tracking of essential regulatory documentation.
The role involves programming, validating, and delivering NONMEM-ready PK/PD datasets while ensuring compliance with SDTM/ADaM standards. The candidate will collaborate with cross-functional teams to resolve data issues and support regulatory submissions through high-quality dataset creation.
The specialist will process and assess safety data, including adverse events, while ensuring compliance with regulatory standards and internal SOPs. They will also collaborate with functional team members and healthcare professionals to manage project-related safety information.
Process and manage safety data and adverse events in accordance with regulatory guidelines and internal SOPs. Collaborate with functional team members and healthcare professionals to ensure quality and compliance across project deliverables.
The Field Nurse Educator provides direct educational training to patients regarding specific disease states and prescribed medications. They coordinate patient resources and foster effective dialogue between patients and their healthcare providers.
The Medical Director serves as a medical monitor for clinical trials, providing scientific expertise and oversight for protocol-related issues and adverse event management. They also contribute to medical strategy by supporting client proposals, bid defenses, and providing guidance to internal stakeholders.
The Senior Director leads complex drug development programs and portfolios, providing strategic oversight and guidance to cross-functional teams. They are responsible for driving operational excellence, managing key customer relationships, and developing high-performing teams to ensure successful program delivery.
The Contracts Manager will review, draft, and redline commercial contracts for IQVIA's services while ensuring alignment with business objectives. They will independently manage high-volume legal reviews and collaborate with internal stakeholders to implement contracting efficiencies.
The Nurse Educator provides remote and in-field patient education regarding disease states and medication adherence to improve treatment outcomes. They also collaborate with healthcare providers and internal leadership to ensure compliance and maintain high educational standards.
Nurse Educators provide direct educational training to patients regarding specific disease states and prescribed medications to improve treatment compliance. They coordinate patient resources and facilitate dialogue between patients and their healthcare providers while maintaining strict adherence to program guidelines.
The specialist will review, assess, and process safety data while ensuring compliance with regulations and internal SOPs. They will also liaise with functional team members and healthcare professionals to address project-related issues.
The Nurse Educator provides remote and in-person patient education, including medication administration training and adherence support. They also facilitate connections to resources and maintain accurate documentation while collaborating with field leadership.
Conduct structured psychiatric assessments and administer validated rating scales for clinical trial participants with Borderline Personality Disorder. Ensure high-quality data collection while maintaining inter-rater reliability and adhering to GCP and safety protocols.
You will lead complex projects from initiation to completion, managing scope, time, budget, and interdisciplinary teams. Additionally, you will be responsible for stakeholder communication, risk management, and driving digital transformation within the organization.
Manage the execution of clinical studies from initiation to closeout while ensuring compliance with SOPs, protocols, and regulatory requirements. Perform remote monitoring, subject-level data reviews, and trend analysis to maintain data integrity and site performance.
The software engineer will enhance and maintain user interfaces for core applications while ensuring performance, usability, and scalability. They will also design, develop, and test new UI features while building the data transfer layer between frontend and backend systems.
The Event Project Support Specialist will manage complex international healthcare events by coordinating with stakeholders, suppliers, and internal teams. Responsibilities include financial reconciliation, project documentation maintenance, and supporting the onsite delivery of live events.
The Nurse Educator provides remote and in-field patient education regarding disease states and medication adherence to empower patients in their treatment journey. They also maintain accurate documentation, collaborate with field leadership, and ensure compliance with program protocols and regulatory standards.
The Senior CRA is responsible for performing site selection, initiation, monitoring, and close-out visits while ensuring compliance with GCP and ICH guidelines. They also manage study progress by tracking regulatory submissions, recruitment, and data integrity.
The Nurse Educator provides remote and in-field patient education, including medication administration training and adherence support, while maintaining accurate documentation and compliance standards. They collaborate with field leadership to facilitate patient resources and foster dialogue between patients and healthcare providers.
The Nurse Educator provides remote and in-field patient education regarding disease states and medication adherence while maintaining accurate documentation and compliance. They also facilitate connections to program-approved resources and collaborate with field leadership to support patient treatment journeys.
The Nurse Educator provides remote and in-field patient education regarding disease states and medication adherence to improve treatment outcomes. They also facilitate connections to program-approved resources and maintain accurate documentation while collaborating with field leadership.
The Nurse Educator provides remote and in-person patient education regarding medication administration and disease management to improve treatment adherence. They also maintain accurate documentation, collaborate with field leadership, and facilitate connections between patients and healthcare resources.
The Nurse Educator provides remote and in-person patient education regarding medication administration and disease management to improve treatment adherence. They also collaborate with healthcare providers and field leadership to maintain program standards and support patients throughout their treatment journey.
The Nurse Educator provides remote and in-field patient education regarding disease states and medication adherence while maintaining accurate documentation and compliance standards. They facilitate connections to program-approved resources and collaborate with field leadership to support patients throughout their treatment journey.
The Nurse Educator provides remote and in-field patient education, including medication administration training and adherence support, while maintaining accurate documentation and compliance standards. They collaborate with healthcare providers and field leadership to empower patients throughout their treatment journey and facilitate access to program-approved resources.
The Nurse Educator delivers remote and in-person patient education regarding disease states and medication adherence to improve health outcomes. They also maintain accurate documentation, collaborate with field leadership, and facilitate connections between patients and approved resources.
The Nurse Educator delivers remote and in-field patient education, including medication administration training and adherence support. They collaborate with healthcare providers and leadership to ensure program compliance and optimal patient health outcomes.
The Medical Director provides medical and scientific expertise for clinical trials, including medical monitoring, protocol review, and safety oversight. They also support business development activities by providing strategic medical advice and participating in client proposals and bid defenses.
The Oncology Sales Specialist will educate and promote oncology therapeutics to key stakeholders within a designated territory to meet patient needs. This role involves collaborating with cross-functional teams and utilizing virtual tools to manage accounts and drive sales objectives.
The Senior Clinical Data Coordinator manages clinical trial data activities, including ongoing data review and reconciliation of third-party and safety data. They are also responsible for performing User Acceptance Testing (UAT) and Quality Control (QC) on clinical databases to ensure high-quality deliverables.
Perform complex rebate calculations for managed care, Medicaid, and government programs while ensuring SLA compliance. Analyze utilization data to create accurate client deliverables and collaborate with onshore US teams.
The Medical Director provides medical and scientific oversight for clinical research programs, serving as the primary medical monitor for sponsor companies. Responsibilities include protocol development, safety monitoring, SAE reporting, and providing medical input for clinical data and regulatory submissions.
The Medical Director provides medical and scientific oversight for clinical research programs, serving as the primary medical monitor for sponsor companies. Responsibilities include protocol development, safety monitoring, SAE reporting, and providing medical expertise to project teams throughout the clinical trial lifecycle.
The Clinical Data Manager oversees the data management aspects of clinical trials to ensure they are completed on time, within budget, and to high quality standards. They act as the primary representative on multidisciplinary teams, managing data metrics, trial documentation, and site training.
The EDC Clinical Trial Designer creates high-quality data collection tools and facilitates the design, development, and testing of clinical eCRF databases. They ensure adherence to standard operating procedures and regulatory requirements while managing project timelines and study team communications.
The Regional Sales Director is responsible for managing a team of Customer Experience Managers to promote pharmaceutical products and meet regional sales objectives. They will oversee personnel development, ensure contractual obligations are met, and act as a liaison between the client and IQVIA.
The role involves managing digital marketing campaign deliverables for healthcare clients and serving as a primary point of contact for internal stakeholders. You will also lead process improvement initiatives and utilize AI-powered tools to enhance operational efficiency and project outcomes.
The analyst provides first-level technical and operational support to clinical trials personnel via phone, email, and chat. They are responsible for resolving routine technical issues, documenting call information, and escalating complex problems to the appropriate support teams.
The analyst provides first-level technical and operational support to clinical trials personnel via phone, email, and chat. They are responsible for resolving routine technical issues, documenting call information, and escalating complex problems to the appropriate support teams.
The Project Manager oversees operational aspects of projects, including tracking timelines, managing budgets, and ensuring compliance with SOPs. They also coordinate with internal and external stakeholders to deliver project milestones and implement process improvements.
Provide first-level technical and operational support to clinical trials personnel via phone, email, and chat. Document call information in a database and escalate complex technical issues to the appropriate support teams.
The Clinical Specialist reviews assessment quality and provides guidance to raters on methodology and scoring techniques. They also participate in calibration activities and ensure the integrity of clinical trial data through live interactions and documentation.
The Clinical Trial Nurse conducts in-home visits to perform study-related procedures, collect biological samples, and document clinical data. They ensure patient safety and protocol compliance while communicating effectively with study teams.
The representative will serve as the primary contact for patients and healthcare professionals to provide payment assistance and program support. Responsibilities include managing card activations, verifying program eligibility, and troubleshooting submission rejections.
The representative will serve as the primary contact for patients and healthcare professionals to provide payment assistance solutions and program support. Responsibilities include managing card activations, verifying program eligibility, and troubleshooting submission rejections via phone, email, or fax.
The representative will serve as the primary contact for patients and healthcare professionals to provide payment assistance and program support. Responsibilities include card activation, verifying program eligibility, and troubleshooting submission rejections.
The Pharmacy Support Call Center Representative provides payment assistance solutions and fields requests regarding card activation, program eligibility, and benefit explanations. They are responsible for documenting information, resolving issues, and escalating complex cases to the appropriate department.
The Nurse Educator provides remote and in-field patient education regarding disease states and medication adherence to improve treatment outcomes. They also maintain accurate documentation, collaborate with field leadership, and facilitate connections between patients and approved resources.
The Nurse Educator provides remote and in-field patient education regarding medication administration and disease management to improve treatment adherence. They also collaborate with field leadership to support territory coverage, maintain accurate documentation, and facilitate connections to program-approved resources.
The Nurse Educator provides remote and in-field patient education regarding medication administration and treatment adherence. They also facilitate connections to program-approved resources and maintain accurate documentation while collaborating with field leadership.
The Nurse Educator delivers remote and in-person patient education regarding disease states and medication adherence to improve treatment outcomes. They also maintain accurate documentation, collaborate with field leadership, and facilitate connections between patients and approved resources.
The Nurse Educator provides remote and in-field patient education regarding medication administration and treatment adherence to empower patients in managing their disease. They also maintain accurate documentation, collaborate with field leadership, and facilitate connections between patients and approved healthcare resources.
The Nurse Educator provides remote and in-field patient education regarding medication administration and treatment adherence to improve health outcomes. They also facilitate communication between patients and healthcare providers while maintaining accurate documentation and compliance with program protocols.
The Flex Nurse Educator provides remote and occasional in-field educational support and medication training to patients with chronic diseases. They facilitate patient-provider dialogue, maintain accurate documentation, and ensure compliance with program protocols and KPIs.
The Flex Nurse Educator provides remote and occasional in-field educational support and medication training to patients with chronic diseases. They facilitate connections to resources, maintain accurate documentation, and collaborate with leadership to ensure program compliance and patient adherence.
The Centralized Monitoring Assistant provides administrative support to clinical study management teams by maintaining study trackers, generating reports, and ensuring compliance with regulatory requirements. They are also responsible for monitoring site performance, identifying risks, and facilitating corrective actions to ensure study quality.
The Medical Director provides medical and scientific oversight for clinical research programs, serving as the primary medical monitor for sponsor-dedicated studies. Responsibilities include protocol development, safety monitoring, SAE reporting, and providing medical expertise to project teams throughout the clinical trial lifecycle.
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 also responsible for documenting resolutions and troubleshooting submission rejections via phone, email, or fax.
The Regulatory and Start Up Specialist serves as the single point of contact for site activation activities, ensuring adherence to regulations and project timelines. They are responsible for preparing and reviewing regulatory documents, maintaining internal databases, and coordinating with project teams to ensure site readiness.
The Regulatory and Start Up Specialist serves as the single point of contact for site activation activities, ensuring adherence to regulations and project timelines. They are responsible for preparing and reviewing regulatory documents, maintaining internal databases, and coordinating with investigative sites and project teams.
You will support the delivery of healthcare marketing campaigns by managing audience selection, mailing list preparation, and campaign documentation. The role involves collaborating with cross-functional teams to ensure quality, traceability, and audit readiness in a regulated environment.
You will support the planning, execution, and monitoring of healthcare marketing campaigns while ensuring quality, traceability, and audit readiness. Additionally, you will focus on standardizing and automating repeatable tasks to improve operational efficiency and capacity.
The Recall Analyst manages and coordinates recall projects by handling inbound and outbound calls with healthcare professionals. They are also responsible for maintaining project documentation, updating internal databases, and ensuring compliance with industry regulations.
The Recall Analyst manages and coordinates recall projects by handling inbound and outbound calls with healthcare professionals. They are also responsible for maintaining accurate project documentation and ensuring compliance with industry standards.
Maintain and update product reference databases for the Dutch market to ensure high levels of data accuracy and integrity. Collaborate with local teams to validate data, resolve discrepancies, and perform regular quality checks.
The Central Independent Rater will administer, score, and review psychiatric assessments such as MINI and MADRS for clinical trials. They will work as part of a global team to support depression studies and ensure accurate clinical data collection.
The Clinical Specialist reviews clinical trial data and assessment scales to ensure standardized practices and data integrity. They also provide guidance to raters through live interactions, feedback, and functional assessments.
The Medical Information Case Processor is responsible for receiving and documenting incoming inquiries from patients and healthcare providers regarding safety data. They must also create accurate Adverse Event and Product Quality Complaint reports while adhering to regulatory guidelines and project requirements.
The Regulatory and Start Up Specialist serves as the primary point of contact for site activation activities, ensuring adherence to regulatory standards and project timelines. They are responsible for preparing and reviewing regulatory documents, maintaining internal databases, and coordinating with project teams to ensure site readiness.
The representative is responsible for receiving and reviewing medical claims against program-specific business rules to determine approval or rejection. They also provide payment assistance solutions and support customer inquiries via various communication channels.
The representative will serve as the primary contact for patients and healthcare professionals to assist with payment programs and benefit explanations. They are responsible for resolving submission rejections, documenting interactions, and escalating complex issues to management.
The specialist will manage site activation activities, including regulatory document preparation and contract negotiations for clinical research sites. They will serve as the primary point of contact for investigative sites and project teams to ensure adherence to timelines and quality standards.
The Clinical Trial Lead is responsible for managing global, cross-functional Phase III clinical trial teams to ensure successful delivery within timelines and quality standards. They also provide strategic oversight, manage trial documentation, and mentor clinical operations staff to ensure compliance and milestone achievement.
The Clinical Specialist supports stroke clinical trials by administering standardized assessments and ensuring data quality. They also review assessments conducted by other raters to maintain protocol compliance and provide feedback on scoring techniques.
The Clinical Specialist supports stroke clinical trials by administering standardized assessments and ensuring data quality. They also review assessments conducted by other raters to maintain protocol compliance and provide feedback on scoring methodology.
The Site Manager will oversee study start-up activities, including ethics committee submissions, site selection, and contract negotiations. They will also collaborate with cross-functional teams to support site management and ensure operational compliance.
The role involves managing client relationships and project delivery for connected devices within clinical research. Responsibilities include developing departmental strategy, overseeing quality control, and ensuring compliance with regulatory guidelines.
The Associate Client Success Director serves as a strategic partner and primary point of contact for enterprise clients, ensuring they achieve measurable business outcomes through Cedar Gate solutions. This role involves leading cross-functional account teams, driving product utilization, and representing the voice of the client to inform product development.
The Regional Specialist will lead site onboarding and coordinate remote patient visits to ensure seamless execution of clinical trials. They will also collaborate with internal and external stakeholders to resolve operational challenges while maintaining high standards of quality and compliance.
The representative will serve as the primary contact for patients and healthcare professionals to provide payment assistance and program support. Responsibilities include managing card activations, verifying program eligibility, and troubleshooting submission rejections.
The Therapeutic Strategy Director leads cross-functional teams to design innovative, client-centric solutions for internal medicine programs during the proposal and business development phase. They are responsible for securing new business, managing high-level client relationships, and ensuring the successful translation of strategy into operational delivery.
The Associate Contracts Analyst develops and prepares contracts, budgets, and scopes of work for assigned customers to support the global sales team. They also ensure that all contract changes are accurately integrated and maintain relevant databases and documentation throughout the study lifecycle.
The Oncology Overlay Sales Specialist will educate and promote oncology therapeutics to key stakeholders while managing a designated territory. This role involves conveying complex clinical and access information to ensure patients receive appropriate therapies through collaborative account management.
The Player/Coach is responsible for managing an assigned territory and promoting products to specialty healthcare providers through outbound and inbound calls. They also manage, develop, and monitor Customer Engagement Specialist Representatives to ensure sales objectives and performance standards are met.
The Associate Director is responsible for driving business growth through a consultative sales approach across pharmaceutical and MedTech accounts. They will identify new opportunities and manage relationships to provide integrated solutions for patient access, affordability, and adherence.
The Senior Project Manager is responsible for leading clinical studies, ensuring project delivery meets contractual requirements, and managing cross-functional teams to achieve milestones. They also oversee project financials, manage stakeholder relationships, and drive operational excellence through strategic planning and risk mitigation.
The Solution Implementation Lead serves as the end-to-end execution owner for developing and operationalizing connected medical device and digital health solutions. They coordinate cross-functional teams including engineering, IT, and regulatory to ensure solutions are ready for scalable study deployment.
Perform monitoring and site management to ensure clinical studies adhere to protocols, regulations, and sponsor requirements. Manage site practices, including recruitment planning, regulatory submissions, and data integrity.
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 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 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 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.
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 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.
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 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.
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.
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 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.
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 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.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
Lead the preparation and delivery of key aggregate safety reports and manage signal detection, validation, and evaluation activities. Collaborate with global cross-functional stakeholders to support safety strategies and regulatory authority inquiries.
The 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.
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.
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. Responsibilities include evaluating assessment quality, conducting live feedback sessions, and supporting rater performance through mock interviews.
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.
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.
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 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.
Lead the development of optimum strategies for drug development, product lifecycle, and portfolio management to meet pharmaceutical customer goals. Provide high-level consultancy on clinical, regulatory, and commercial strategies from discovery to market.
Provide appropriate responses to inquiries from medical institutions and the general public while collecting and reporting adverse event information to clients. Perform supervisor duties including quality improvement, progress management, problem solving, and member support.
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.
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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 Registered Dietitian will conduct comprehensive nutritional assessments and provide ongoing counseling and motivational support to study participants. They will monitor participant progress and collaborate with the clinical research team to ensure adherence to study protocols.
The Registered Dietitian will conduct comprehensive nutritional assessments and provide ongoing counseling and motivational support to study participants. They will monitor participant progress and collaborate with the clinical research team to ensure adherence to study protocols.
The Registered Dietitian will conduct comprehensive nutritional assessments and provide ongoing counseling and motivational support to study participants. They will monitor participant progress and collaborate with the clinical research team to ensure adherence to study protocols.
The Medical Writer will be responsible for creating clinical trial-related documents such as protocols, clinical study reports, and CTD modules, as well as authoring post-marketing surveillance documents and clinical study reports/papers. They will also perform Quality Control (QC) checks on various documents.
The Lead Medical Writer will be responsible for creating and reviewing clinical trial documents such as protocols, CSRs, and CTDs, as well as adapting global protocols for Japanese requirements. Responsibilities also include managing projects, resources, budgets, client interactions, and mentoring junior staff.
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.
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 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 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 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.
