This role involves leading complex, client-facing revenue management and system integration engagements while managing and developing a team of functional and technical resources. The principal will own end-to-end implementations and provide subject matter expertise across the pharmaceutical revenue management ecosystem.
The Associate Medical Director provides medical, clinical, and scientific advisory expertise for assigned clinical trials and business development activities. Responsibilities include medical monitoring, protocol review, and providing strategic guidance to internal stakeholders and investigative sites.
The Medical Strategy Lead will drive the growth of the Cell and Gene Therapy portfolio by providing scientific and clinical expertise to develop innovative, patient-centered trial solutions. They are responsible for leading business development activities, guiding sponsors, and ensuring the scientific and regulatory soundness of clinical development plans.
The role provides scientific support for epidemiology studies by conducting literature reviews, data cleaning, and quality control activities. It also involves coordinating operational tasks across multiple studies to ensure high-quality execution and cross-functional alignment.
The Statistical Scientist will lead complex clinical studies, develop protocols, and create analysis plans while ensuring data integrity and regulatory compliance. They are responsible for interpreting clinical trial data, writing statistical sections of reports, and managing project timelines and resources.
The Security Program Manager will gather, analyze, and manage requirements for enterprise IAM solutions to ensure alignment with business and regulatory standards. They will collaborate with engineering, QA, and operations teams to support the full SDLC, from discovery through release and onboarding.
The Central Monitor is responsible for the centralized review of study and site-level risk signals to ensure data quality and patient safety. They analyze clinical and operational data to identify trends and provide actionable recommendations to study teams and CRAs for risk mitigation.
Develop and manage investigator grants, contracting strategies, and site agreements to support clinical trial initiation and maintenance. Collaborate with sponsors and internal stakeholders to ensure contracting efficiency, compliance with regulatory requirements, and adherence to project timelines.
The Clinical Specialist reviews rater-administered scales in clinical trials to ensure data reliability and standardized assessment procedures. They provide guidance to raters on methodology and scoring techniques through live interactions and functional performance assessments.
The role involves conducting virtual medical visits to healthcare professionals to communicate scientific and promotional product information. The representative will also manage relationships with doctors and maintain accurate records in the CRM system.
You will design, develop, and maintain scalable web applications with a primary focus on React-based front-end development. Additionally, you will collaborate with cross-functional teams to deliver high-quality technical solutions and provide production support for complex incidents.
The Player/Coach is responsible for managing an assigned territory and promoting products to specialty healthcare providers through inbound and outbound calls. They also oversee, develop, and monitor Customer Engagement Specialist Representatives to ensure sales objectives and performance standards are met.
The Medical Data Review Manager is responsible for reviewing structured clinical patient data to ensure medical plausibility and protocol adherence. They will identify data anomalies, verify adverse events, and ensure the overall readiness of patient information for subsequent review levels.
The Survey Quality Assurance Specialist is responsible for testing and validating survey instruments to ensure accuracy, functionality, and compliance with project requirements. They monitor surveys during fielding, document defects, and collaborate with cross-functional teams to maintain high data quality standards.
The 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 investigative sites and internal stakeholders to ensure efficient contract execution and regulatory compliance.
The role involves planning, coordinating, and delivering exhibition booths for industry tradeshows while supporting corporate marketing and internal events. You will manage project timelines, budgets, and supplier relationships to ensure high-quality event delivery and positive stakeholder experiences.
The Medical Strategy Lead provides strategic medical and scientific expertise to support clinical development plans and proposal development within the Hematology-Oncology Center of Excellence. They act as an internal and external consultant throughout the research and development lifecycle, guiding project teams and sponsors on clinical strategy and study execution.
The TMF Quality Project Manager serves as a liaison between Records Management and user departments to ensure clinical research records are maintained according to SOPs and regulatory requirements. They oversee the transfer, imaging, and disposition of project records while providing functional leadership to project teams.
The Associate Centralized Monitor supports clinical trial delivery by reviewing site data, performance metrics, and risks to ensure compliance and data integrity. They collaborate with project teams and sites to resolve queries and maintain essential study documentation.
Lead end-to-end data management for complex, global clinical trials from study setup to database lock. Serve as the primary client contact while overseeing data reconciliation, timelines, and budgets.
You will act as a liaison between clients and technical teams to define business use cases and translate analytical concepts into actionable recommendations. Additionally, you will manage multi-disciplinary projects, mentor junior staff, and support business development through client pitches and proposals.
The Centralized Monitoring Analyst is responsible for setting up and programming the Centralized Monitoring platform, including QTLs, KRIs, and data visualizations. They also support the Centralized Monitoring Lead in developing study-specific strategies and maintaining platform specifications.
The specialist manages site activation activities, including feasibility assessments, regulatory documentation, and site identification. They also negotiate contracts and budgets while serving as the primary point of contact for investigative sites.
The analyst will evaluate and support the development of AI-enabled healthcare analytics solutions to improve provider performance insights. They will collaborate with cross-functional teams to translate business requirements into effective analytical capabilities and validate AI-generated outputs.
The Senior Product Owner will define and execute the product vision and roadmap for population health and value-based care solutions. They will lead cross-functional teams and act as the primary advocate for customers to ensure the delivery of high-value, scalable software capabilities.
The Project Lead manages the delivery of Site Enablement Solutions by coordinating planning, implementation, and operational strategies across global clinical trials. They act as internal consultants to study teams and sponsors, ensuring projects meet financial performance goals and quality standards.
Perform centralized monitoring activities to evaluate the quality and integrity of clinical studies according to protocols and regulations. Manage study-specific data, prepare site packs, and collaborate with cross-functional teams to resolve data issues.
The engineer will provide third-tier AV and IT support, manage conference room fleets, and ensure hardware and installation standards are met. They are also responsible for developing technical documentation, training end-users, and performing system maintenance and security administration.
The Project Coordinator manages ongoing projects across the life sciences industry, including brand strategy, advisory boards, and various events. They are responsible for maintaining client relationships, tracking project deliverables, and ensuring all work meets quality and timeline expectations.
The manager is responsible for overseeing clinical operations staff, ensuring projects are properly resourced, and maintaining high quality and performance standards. They also handle onboarding, training, and professional development for team members while collaborating with cross-functional teams.
Perform site selection, initiation, monitoring, and close-out visits to ensure study compliance with protocols and regulations. Manage site progress by tracking regulatory submissions, recruitment, and data query resolution.
Conduct outbound calls to healthcare professionals to collect, verify, and record key information in the database. Perform match activities, documentation, and troubleshooting to ensure data accuracy according to project guidelines.
The Senior Director provides strategic leadership and consultancy for drug development, product lifecycle management, and portfolio management to meet customer goals. They are responsible for guiding regulatory strategies, leading cross-functional teams, and supporting business development activities to drive organizational growth.
The Contract Negotiator will support start-up contracting activities, including developing grant estimates and managing contract templates for clinical trials. They will collaborate with sponsors and internal stakeholders to ensure compliance with regulatory requirements and project timelines.
The internal translator is responsible for accurately interpreting written material while maintaining the original structure, style, and facts. They will also collaborate with the translation services team to manage glossaries, translation memories, and style guides while proofreading content for accuracy.
The specialist will conduct site feasibility assessments and investigator outreach across Poland, Hungary, and the Czech Republic. They will also support study start-up activities, including EU CTR document collection and essential site document review.
The specialist serves as the single point of contact for investigative sites and project teams to manage site activation activities and regulatory documentation. They are responsible for ensuring adherence to SOPs, maintaining project timelines, and performing quality control on site-related documents.
The Site Activation Specialist manages feasibility, site identification, regulatory start-up, and maintenance activities for clinical trials. They serve as the primary point of contact for investigative sites and ensure all documentation and contracts are executed according to project timelines.
The Data Acquisition Specialist is responsible for defining, setting up, and ingesting external data streams in alignment with clinical trial protocols. They will liaise with stakeholders and external providers to ensure data transfer agreements are accurate and compliant with regulatory standards.
The Associate Medical Director provides strategic scientific leadership across client accounts and leads, mentors, and develops a team of medical and scientific professionals. They serve as a senior advisor to clients, ensuring the quality and integrity of deliverables while driving operational excellence and business growth.
This role provides scientific and strategic leadership for real-world evidence and epidemiology studies, serving as the primary lead for assigned scientific workstreams. The incumbent ensures scientific rigor, operational feasibility, and quality across study protocols, publications, and analytical deliverables.
The role involves aligning sales, consulting, and product management to drive growth strategies for MedTech and IVD industry clients. You will lead the development of competitive technology offerings and manage global teams to execute strategic initiatives.
Direct and manage the strategic, operational, and financial execution of site activation activities, including site selection, regulatory processes, and contract negotiations. Collaborate with internal and external stakeholders to ensure project timelines and quality standards are met throughout the clinical study lifecycle.
Lead and manage the strategic, operational, and financial delivery of site activation activities across assigned studies and regions. Oversee regulatory submissions, site contracting, and project timelines to ensure efficient study start-up and patient enrollment.
The Clinical Research Associate II participates in the preparation and execution of Phase I-IV clinical trials while overseeing site evaluation, initiation, and monitoring activities. They ensure compliance with Good Clinical Practices and maintain data integrity through source verification and site correspondence.
Lead and manage the strategic, operational, and financial delivery of site activation activities across assigned studies and regions. Collaborate with internal and external stakeholders to ensure efficient study start-up, regulatory compliance, and timely patient enrollment.
Lead and manage the strategic, operational, and financial delivery of site activation activities across assigned studies and regions. Collaborate with internal and external stakeholders to ensure efficient study start-up, regulatory compliance, and timely patient enrollment.
Perform site activation, feasibility, and maintenance activities for clinical research studies in accordance with SOPs and regulations. Manage project documentation, track progress, and collaborate with internal teams to ensure site readiness.
You will lead the product strategy and lifecycle for measurement studies, platform reporting, and data services within the healthcare marketing ecosystem. This involves collaborating with cross-functional teams to drive product adoption, manage roadmaps, and deliver actionable insights that optimize client marketing performance.
Responsible for promoting the cardiometabolic portfolio to medical specialists via web and telephone platforms. Ensures brand adoption and meets established sales goals while maintaining effective relationships with the medical panel.
The supervisor will coordinate and develop virtual medical visit teams to ensure commercial objectives and quality standards are met. They are responsible for managing remote talent, analyzing performance data, and strengthening relationships with healthcare clients.
The role involves administering, scoring, and reviewing psychiatric assessments such as MINI and MADRS for a depression study. You will act as a Central Independent Rater to support clinical trial data integrity.
The role involves administering, scoring, and reviewing psychiatric assessments such as MINI and MADRS for a depression study. You will act as a Central Independent Rater to support clinical trial data integrity.
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 proposals and pitch materials.
The role involves managing and coding medical data collected from healthcare settings to support pharmaceutical research and market analysis. Responsibilities include data entry, quality control, data cleansing, and mapping to ensure high-quality information for clinical development.
The Solution Sales Specialist will identify and develop new business opportunities while maintaining strong relationships with key decision-makers in the pharmaceutical and life sciences sectors. They are responsible for executing sales plans, delivering consultative solutions, and acting as a primary liaison between clients and internal operational teams.
The Project Management Analyst supports clinical trial delivery by managing project schedules, finances, and risk mitigation strategies. They also maintain performance dashboards and ensure accurate reporting to facilitate effective decision-making for project leaders.
The Central Monitor performs centralized monitoring activities to ensure the quality and integrity of clinical studies according to protocols and regulations. They also manage site triggers, prepare site packs, and interact with cross-functional teams to resolve data issues.
The Clinical Study Manager is responsible for the operational and scientific oversight, setup, and execution of clinical trials at the local level. They lead cross-functional teams, manage site activities, and ensure data quality and compliance with regulatory standards.
The specialist will manage site activation activities and serve as the primary point of contact for investigative sites and project teams. They are responsible for preparing regulatory documents, ensuring adherence to SOPs, and tracking project timelines to meet clinical research objectives.
The Practice Lead will oversee a specialized medical and scientific communications business, focusing on driving growth, client retention, and operational excellence. They will lead cross-functional teams to deliver integrated, technology-enabled solutions while fostering a collaborative and high-performing culture.
The Senior Clinical Research Associate is responsible for site management and monitoring activities across the country for a single sponsor. They will drive subject recruitment plans, provide protocol training, and maintain monitoring visit reports.
You will perform site selection, initiation, monitoring, and close-out visits while ensuring adherence to Good Clinical Practice and study protocols. Additionally, you will manage study progress by tracking regulatory submissions, recruitment, and data query resolution.
The Principal Biostatistician serves as the statistical lead for late-phase clinical trials, providing scientific oversight and strategic guidance. They are responsible for authoring statistical analysis plans, performing complex analyses, and representing the biostatistics function within cross-functional clinical teams.
Lead the full scope of biostatistics conduct for therapeutic programs, including defining statistical strategy and methodologies for clinical trials. Collaborate with cross-functional teams to ensure high-quality delivery of results for regulatory submissions and clinical development plans.
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 clinical research outcomes.
The role involves driving sales and account management activities within the European biotech sector to expand the client base. Responsibilities include developing robust account strategies and managing high-level relationships with C-suite executives to sell integrated clinical solutions.
Define the product vision and roadmap for agentic AI initiatives to streamline clinical trial workflows. Lead cross-functional teams to translate business needs into scalable AI solutions while tracking performance metrics.
The Director will drive global business development by identifying market opportunities and executing strategies for commercial outsourcing and engagement solutions. They will act as a strategic advisor to senior clients while leading complex, multi-country proposal development and cross-functional teams.
The Associate Director manages client relationships and leads account teams to ensure project deliverables meet operational excellence standards. They are responsible for driving organic business growth, mentoring staff, and maintaining alignment with company strategy and goals.
The Clinical Data Manager oversees the data management lifecycle for clinical trials, ensuring high-quality data collection and adherence to regulatory standards. They act as the primary data representative on project teams, managing study documentation, metrics, and cross-functional communication.
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.
The Data Acquisition Specialist is responsible for defining, setting up, and ingesting external data streams in alignment with clinical trial protocols. They liaise with stakeholders and external providers to ensure data accuracy, compliance, and timely transfer for clinical monitoring and analysis.
The Medical Director provides medical, clinical, and scientific advisory expertise for clinical trials and business development activities. Responsibilities include medical monitoring, protocol review, safety oversight, and strategic support for client proposals.
The coordinator will perform site activation, feasibility, and maintenance activities for clinical research studies while ensuring regulatory compliance. They are responsible for preparing, reviewing, and distributing site documents and maintaining internal project tracking systems.
Manage contract strategy and oversee all start-up contracting activities for complex clinical studies and multi-protocol programs. Collaborate with sponsors and internal teams to ensure high-quality delivery, compliance, and efficient study initiation.
The Senior Site Contracts Associate manages contract strategy and oversees all start-up contracting activities for complex clinical studies. They also collaborate with sponsors and internal teams to ensure operational excellence, compliance, and accurate financial reporting.
The Senior Decentralized Clinical Trial Study Lead is responsible for the strategic development and delivery of decentralized clinical trials, ensuring they meet quality, speed, and financial objectives. They act as the primary point of contact for customers and lead cross-functional teams to manage study milestones, risks, and project performance.
Manage contract strategy and oversee start-up contracting activities for complex clinical studies and multi-protocol programs. Collaborate with sponsors and internal teams to ensure operational excellence, compliance, and the delivery of high-quality site agreements.
The Clinical Research Associate is responsible for performing site selection, initiation, monitoring, and close-out visits while maintaining accurate documentation. They also manage study progress by tracking regulatory submissions, recruitment plans, and data integrity.
The Senior Site Contracts Associate will manage contract strategy and oversee all start-up contracting activities for complex clinical studies. They will also collaborate with sponsors and regional teams to ensure operational excellence, compliance, and accurate financial reporting.
The Central Independent Rater will administer, score, and review psychiatric assessments for a depression study. You will work as part of a global team to support clinical trial data integrity and patient outcomes.
The Senior Director will lead global sales strategy and build strategic partnerships within the Emerging Biopharma portfolio to drive revenue growth. They will orchestrate cross-functional teams to deliver integrated solutions that address customer development and commercialization priorities.
The Senior Business Analyst will lead the gathering, analysis, and validation of software requirements for the clinical eSource platform. They will collaborate with cross-functional teams to translate business needs into functional specifications and technical documentation.
The Database Operator is responsible for maintaining, validating, and enhancing product and customer databases for the Danish market. They will perform data cleansing, generate reports, and collaborate with international teams to ensure high data accuracy.
The Database Operator will maintain and update product reference databases for the Norwegian market to ensure high data accuracy and integrity. They will also collaborate with local teams to resolve data discrepancies and contribute to continuous improvement initiatives.
The Senior Business Analyst will lead the gathering, analysis, and validation of software requirements for clinical trial automation systems. They will collaborate with cross-functional teams to translate business needs into functional specifications and technical documentation.
Perform site monitoring visits to ensure compliance with regulatory requirements and Good Clinical Practice guidelines. Manage study progress by tracking regulatory submissions, subject recruitment, and data integrity across assigned clinical sites.
The Senior Project Manager will oversee the full lifecycle of eCOA implementation projects, managing scope, budget, timelines, and internal staff. They will also serve as the primary liaison between internal teams and clients to ensure high-quality service delivery and strong customer relationships.
The Clinical Research Associate II is responsible for monitoring Phase I–IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. They manage site activities from start-up through close-out, including site visits, training, and documentation quality assurance.
The coordinator supports clinical laboratory projects throughout the study lifecycle by managing daily operations, monitoring performance, and ensuring high-quality deliverables. They also facilitate study start-up, handle protocol-specific documentation, and maintain communication with internal and external stakeholders.
The Senior Medical Director provides scientific, clinical, and operational oversight for global clinical research programs while serving as the primary medical monitor. They are responsible for ensuring patient safety, interpreting clinical data, and guiding study teams through protocol execution and regulatory interactions.
The Medical Science Liaison will drive pre-launch medical readiness for HDV by mapping key centers and building credible peer-to-peer scientific relationships with healthcare professionals. Additionally, the role involves gathering actionable field insights and providing secondary support for clinical trial execution.
The Director will lead and develop a team of agency-focused sellers to drive revenue growth and expand the adoption of IQVIA Digital solutions. They will build and manage strategic relationships with key agency partners while overseeing pipeline development and go-to-market strategies.
The Senior Safety Project Lead manages service delivery excellence for assigned projects, acting as the primary point of contact for internal and external customers. They are responsible for project planning, financial management, and ensuring compliance with regulatory requirements throughout the product lifecycle.
The manager will drive awareness and uptake of a vaccine portfolio through virtual engagement with healthcare professionals and key stakeholders. They are responsible for developing business plans, delivering clinical education, and gathering market insights to maximize account performance.
The Product Manager will manage and prioritize product enhancements for the Capitation Adjudication platform while collaborating with cross-functional teams to define requirements. They will also support implementation, testing, and release activities to ensure the platform meets client and business needs.
The Client Services Director is responsible for managing client accounts, overseeing project timelines, and ensuring the scientific accuracy of deliverables. They also facilitate communication between internal departments and external stakeholders to drive long-term account planning and brand strategy.
The Global Clinical Project Manager is responsible for overseeing vendor activities across the study lifecycle to ensure high-quality deliverables and operational efficiency. They will manage vendor performance, track KPIs, and coordinate study start-up and close-out activities.
The Global Clinical Project Manager is responsible for overseeing vendor deliverables across the clinical trial lifecycle to ensure quality and efficiency. Key tasks include managing vendor performance, supporting site activation, and coordinating study close-out activities.
The specialist will manage the collection, review, and preparation of regulatory documentation for UK clinical trial submissions. They will also coordinate Informed Consent Form adaptations and liaise with investigative sites to ensure submission packages are compliant and timely.
The role involves conducting patient interviews and clinical assessments while ensuring the integrity and reliability of clinical trial data. The rater will provide guidance to other raters on methodology and scoring techniques through live interactions.
The Clinical Independent Rater ensures the integrity of clinical trial data by reviewing assessment quality and providing guidance to raters. Responsibilities include conducting live interactions with raters to provide feedback on methodology and scoring techniques.
The Virtual Patient Educator provides education and resources to patients regarding diabetes treatments and prescribed medications. They conduct one-on-one communications with patients via telephone, video, email, and SMS while maintaining accurate documentation.
The role involves overseeing end-to-end SDTM activities, including CRF design management and ensuring vendor specifications comply with CDISC standards. You will collaborate with sponsor colleagues and CRO partners to plan data receipt and ensure the quality and completeness of SDTM datasets.
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 techniques, and performance support.
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 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.
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.
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 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.
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 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 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.
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.
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 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.
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.
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 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 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-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-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 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.
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 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 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 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 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 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 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 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 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 investigative sites and project teams.
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 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 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 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 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 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 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 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.
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 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.
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.
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 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.
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.
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.
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 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 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.
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.
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.
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.
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.
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 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 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. Responsibilities include evaluating assessment quality, conducting live feedback sessions, and supporting rater performance through mock interviews.
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 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.
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.
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.
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.
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.
Perform site monitoring visits including selection, initiation, and close-out while ensuring adherence to GCP and ICH guidelines. Manage study progress by tracking recruitment, regulatory approvals, and maintaining essential trial documentation.
Lead 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.
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.
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.
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.
The Associate Site Activation Manager designs and implements strategies for site activation from award to enrollment. They lead country operations teams to ensure client commitments are delivered on time, within scope, and according to budget.
Lead the strategic and operational delivery of global site activation activities to accelerate patient enrollment. This includes managing site identification, regulatory submissions, and contracting in compliance with ICH-GCP standards.
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.
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.
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 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. Monitor patient progress and adherence while maintaining accurate clinical documentation for 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. 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 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.
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 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.
