At IQVIA, we are continuously expanding the boundaries of what's possible in clinical development through advanced analytics, cutting-edge technology, and deep scientific expertise. Within our Research & Development Solutions (RDS) organization, we are enhancing our services with agentic systems-autonomous AI agents that can reason, plan, act, and learn-to further streamline clinical trial workflows and accelerate the delivery of new therapies. By embedding these capabilities into our service offerings for our customers and the clinical sites that we engage with to run clinical trials, we not only strengthen our leadership in AI-driven clinical research, but also bring life-changing treatments to patients faster and more efficiently. Are you ready to lead and shape the future of Generative AI in life sciences? As a Senior AI Scientist at IQVIA, you will play a pivotal role in architecting, developing, and deploying cutting-edge AI/ML solutions that transform how pharmaceutical companies operate and innovate. You will work at the forefront of machine learning, leading initiatives that leverage large language models (LLMs), agentic AI, and advanced optimization techniques to deliver real-world impact. Role Summary: IQVIA's AI Scientist Group is a strategic innovation unit that delivers tailored, state-of-the-art AI solutions to pharmaceutical and life sciences clients. As a Senior AI Scientist, you will lead the design and execution of AI strategies, drive model development and experimentation, and guide both internal and external stakeholders through the implementation of scalable Generative AI solutions. Key Responsibilities: Lead the fine-tuning, distillation, and deployment of LLMs for high-impact use cases in clinical research and commercial life sciences. Drive data engineering processes to convert structured and unstructured data into high-quality, trainable datasets. Design and implement AI agents using IQVIA's Agentic AI framework to enable autonomous reasoning and task completion. Spearhead the development of proof-of-concept models and guide transition to production-ready systems. Stay at the forefront of advances in LLMs and generative techniques; evaluate and apply relevant methodologies such as SFT, PPO, and reward modeling. Provide technical leadership and mentorship to junior scientists and engineers. Serve as a key technical voice in client engagements-translating complex AI concepts into actionable business insights. Collaborate cross-functionally with engineering, product, and domain experts to ensure AI solutions align with customer needs and compliance frameworks. Contribute to publication strategies and represent IQVIA at leading AI/ML conferences (e.g., NeurIPS, ICML, ICLR). Qualifications: PhD in Computer Science, Machine Learning, Artificial Intelligence, or a related field, with a strong publication record in top-tier AI conferences. Extensive experience with fine-tuning/distillation of large-scale language models, with hands-on expertise in SFT, PPO, and reward modeling. Deep proficiency in Python and AI/ML frameworks such as PyTorch, LangChain, LangGraph, GraphRAG, and AutoGen. Experience with modern vector and graph databases (e.g., ChromaDB, Neo4j) and LLMOps platforms (e.g., Azure, Databricks, Azure OpenAI). Proven track record of delivering scalable AI solutions in enterprise settings, preferably in life sciences. Excellent communication and interpersonal skills, with the ability to lead projects and consult directly with senior stakeholders. Experience managing multiple projects, driving timelines, and delivering high-quality results in fast-paced environments. Bonus: Experience in deploying multi-agent frameworks and retrieval-augmented generation (RAG) pipelines. Familiarity with regulatory and privacy considerations in healthcare AI applications. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at
Aug 03, 2025
Full time
At IQVIA, we are continuously expanding the boundaries of what's possible in clinical development through advanced analytics, cutting-edge technology, and deep scientific expertise. Within our Research & Development Solutions (RDS) organization, we are enhancing our services with agentic systems-autonomous AI agents that can reason, plan, act, and learn-to further streamline clinical trial workflows and accelerate the delivery of new therapies. By embedding these capabilities into our service offerings for our customers and the clinical sites that we engage with to run clinical trials, we not only strengthen our leadership in AI-driven clinical research, but also bring life-changing treatments to patients faster and more efficiently. Are you ready to lead and shape the future of Generative AI in life sciences? As a Senior AI Scientist at IQVIA, you will play a pivotal role in architecting, developing, and deploying cutting-edge AI/ML solutions that transform how pharmaceutical companies operate and innovate. You will work at the forefront of machine learning, leading initiatives that leverage large language models (LLMs), agentic AI, and advanced optimization techniques to deliver real-world impact. Role Summary: IQVIA's AI Scientist Group is a strategic innovation unit that delivers tailored, state-of-the-art AI solutions to pharmaceutical and life sciences clients. As a Senior AI Scientist, you will lead the design and execution of AI strategies, drive model development and experimentation, and guide both internal and external stakeholders through the implementation of scalable Generative AI solutions. Key Responsibilities: Lead the fine-tuning, distillation, and deployment of LLMs for high-impact use cases in clinical research and commercial life sciences. Drive data engineering processes to convert structured and unstructured data into high-quality, trainable datasets. Design and implement AI agents using IQVIA's Agentic AI framework to enable autonomous reasoning and task completion. Spearhead the development of proof-of-concept models and guide transition to production-ready systems. Stay at the forefront of advances in LLMs and generative techniques; evaluate and apply relevant methodologies such as SFT, PPO, and reward modeling. Provide technical leadership and mentorship to junior scientists and engineers. Serve as a key technical voice in client engagements-translating complex AI concepts into actionable business insights. Collaborate cross-functionally with engineering, product, and domain experts to ensure AI solutions align with customer needs and compliance frameworks. Contribute to publication strategies and represent IQVIA at leading AI/ML conferences (e.g., NeurIPS, ICML, ICLR). Qualifications: PhD in Computer Science, Machine Learning, Artificial Intelligence, or a related field, with a strong publication record in top-tier AI conferences. Extensive experience with fine-tuning/distillation of large-scale language models, with hands-on expertise in SFT, PPO, and reward modeling. Deep proficiency in Python and AI/ML frameworks such as PyTorch, LangChain, LangGraph, GraphRAG, and AutoGen. Experience with modern vector and graph databases (e.g., ChromaDB, Neo4j) and LLMOps platforms (e.g., Azure, Databricks, Azure OpenAI). Proven track record of delivering scalable AI solutions in enterprise settings, preferably in life sciences. Excellent communication and interpersonal skills, with the ability to lead projects and consult directly with senior stakeholders. Experience managing multiple projects, driving timelines, and delivering high-quality results in fast-paced environments. Bonus: Experience in deploying multi-agent frameworks and retrieval-augmented generation (RAG) pipelines. Familiarity with regulatory and privacy considerations in healthcare AI applications. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at
IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the medical product lifecycle. The Patient Centered Solutions (PCS) team leads the industry in generating data to ensure that the patient voice is incorporated into the development and commercialization of medication and other drug/non-drug interventions. We focus on understanding and meeting the needs of our customers (mostly life science/pharmaceutical companies) through the application of broad consulting expertise and technical scientific knowledge to design scientifically rigorous research to capture insights about patient priorities, needs, preferences and experiences. This research is broad and includes qualitative (e.g., interviews, focus groups), quantitative (e.g., clinical outcome assessments COAs /patient-reported outcomes PROs , preference research) and passive (e.g., digital health technology tools) approaches to understand patient, caregiver and healthcare professional experiences and expectations of disease and treatment. Individuals joining us are assured of a rewarding and progressive career in life sciences consulting. They have the opportunity to address challenging client issues, across multiple geographies with a hands-on influence in delivering solutions. We operate in a truly multi-cultural, collegial, and collaborative work environment that is rich in development and growth. Role & Responsibilities The Head of the Center of Excellence (CoE) for Regulatory Strategy sits within the COA consulting business of PCS and plays a key role in its global leadership team. This individual is a true expert in both the guidance and the practice of developing strategies to engage US FDA, the EMA and other regulatory agencies on COA endpoints and the use of Patient Experience Data (PED) in a regulatory context. This individual fulfills three key functions: 1) bringing their own expertise to bear in proposals, to project delivery, and to customers in support of business growth and impact; 2) developing the regulatory capabilities of the PCS consulting organization through training, process improvement and mentorship; and 3) maintaining an active external profile and involvement in the regulatory landscape for PED. Key responsibilities are: Customer-facing activities Develop and deliver insightful, value-added regulatory strategies that address complex client issues relating to COA endpoints and PED Support sales efforts by providing regulatory subject matter expertise to customer meetings and proposals Support delivery teams who are executing PCS projects with a regulatory component, and ensure we provide consistently high quality insights and content Support billable projects as SME and/or study lead, per study requirements, at 40% utilization or greater Capability building Support community building with activities including recruitment, coaching, management of resources and network development (both juniors and seniors) to collaborate with for regulatory delivery and/or business development purposes Directly line manage a small global team of regulatory specialists Mentor, coach, and share subject matter expertise with others to help develop individuals and capabilities delivering world-class solutions for clients Provide training, templates, and oversight to upskill team and ensure consistent high quality consulting and written deliverables Participate in annual performance review team processes Engage in recruitment and selection of new staff External profile Develop and oversee the PCS thought leadership agenda for the regulatory capability. Represent IQVIA in external working groups and consortia Lead development of IQVIA's responses to public consultation processes from FDA and other regulatory agencies relating to PED Contribute to the enhanced awareness of PCS in the marketplace, e.g., through speaking engagements, client meetings, and publications Develop and facilitate understanding of emerging regulatory practices, expectations and engagements outside of the US FDA and EMA In addition, take on other leadership responsibilities as needed, including: Member of global PCS consulting leadership team and scientific leadership team Provide regulatory subject matter expertise related to PED to the broader PCS organisation (e.g. to instrument ownership and licensing business, and to the implementation services business) About You Candidates interested this position will have: Advanced degrees and 15+ years of experience in PED research, including COA science, preference research, and regulatory engagement (US FDA essential, EMA and other regulatory agencies desirable) Experience working in a regulatory agency and/or demonstrable track record of developing and executing a COA endpoint strategy with successful outcome of COA label claim Experience preparing for, and participating in Type B and Type C meetings with FDA Experience in developing patient experience materials for regulatory consultations and submissions (e.g. COA dossier, briefing documents for Type B/C/D consultations) An understanding of the global regulatory environment as it pertains to PED Strong scientific consulting skills and track record of contributing to business development in a consulting environment Experience of medical writing for various audiences, including pharmaceutical companies, healthcare professionals, regulatory bodies and patients Publications and recognition in the field through participation in industry consortia or scientific bodies. Experienced public speaker Well-developed written and verbal communication skills including presentations, business and report writing An entrepreneurial nature and interest in developing new client offerings and solutions Demonstrable analytical, interpretative, and problem-solving skills Excellent interpersonal skills and ability to work effectively with others An ability to work in a fast-paced environment with demonstrated ability to effectively manage multiple tasks An ability to establish and maintain effective working relationships in multi-disciplinary and international teams Fluency in English (spoken and written) Willingness and ability to travel from time to time Right to live and work in the recruiting country Physical requirements: Extensive use of telephone communication requiring accurate perception of speech. Extensive use of keyboard requiring repetitive motion of fingers. Regular sitting for extended periods of time. Travel as required. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at
Jul 13, 2025
Full time
IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the medical product lifecycle. The Patient Centered Solutions (PCS) team leads the industry in generating data to ensure that the patient voice is incorporated into the development and commercialization of medication and other drug/non-drug interventions. We focus on understanding and meeting the needs of our customers (mostly life science/pharmaceutical companies) through the application of broad consulting expertise and technical scientific knowledge to design scientifically rigorous research to capture insights about patient priorities, needs, preferences and experiences. This research is broad and includes qualitative (e.g., interviews, focus groups), quantitative (e.g., clinical outcome assessments COAs /patient-reported outcomes PROs , preference research) and passive (e.g., digital health technology tools) approaches to understand patient, caregiver and healthcare professional experiences and expectations of disease and treatment. Individuals joining us are assured of a rewarding and progressive career in life sciences consulting. They have the opportunity to address challenging client issues, across multiple geographies with a hands-on influence in delivering solutions. We operate in a truly multi-cultural, collegial, and collaborative work environment that is rich in development and growth. Role & Responsibilities The Head of the Center of Excellence (CoE) for Regulatory Strategy sits within the COA consulting business of PCS and plays a key role in its global leadership team. This individual is a true expert in both the guidance and the practice of developing strategies to engage US FDA, the EMA and other regulatory agencies on COA endpoints and the use of Patient Experience Data (PED) in a regulatory context. This individual fulfills three key functions: 1) bringing their own expertise to bear in proposals, to project delivery, and to customers in support of business growth and impact; 2) developing the regulatory capabilities of the PCS consulting organization through training, process improvement and mentorship; and 3) maintaining an active external profile and involvement in the regulatory landscape for PED. Key responsibilities are: Customer-facing activities Develop and deliver insightful, value-added regulatory strategies that address complex client issues relating to COA endpoints and PED Support sales efforts by providing regulatory subject matter expertise to customer meetings and proposals Support delivery teams who are executing PCS projects with a regulatory component, and ensure we provide consistently high quality insights and content Support billable projects as SME and/or study lead, per study requirements, at 40% utilization or greater Capability building Support community building with activities including recruitment, coaching, management of resources and network development (both juniors and seniors) to collaborate with for regulatory delivery and/or business development purposes Directly line manage a small global team of regulatory specialists Mentor, coach, and share subject matter expertise with others to help develop individuals and capabilities delivering world-class solutions for clients Provide training, templates, and oversight to upskill team and ensure consistent high quality consulting and written deliverables Participate in annual performance review team processes Engage in recruitment and selection of new staff External profile Develop and oversee the PCS thought leadership agenda for the regulatory capability. Represent IQVIA in external working groups and consortia Lead development of IQVIA's responses to public consultation processes from FDA and other regulatory agencies relating to PED Contribute to the enhanced awareness of PCS in the marketplace, e.g., through speaking engagements, client meetings, and publications Develop and facilitate understanding of emerging regulatory practices, expectations and engagements outside of the US FDA and EMA In addition, take on other leadership responsibilities as needed, including: Member of global PCS consulting leadership team and scientific leadership team Provide regulatory subject matter expertise related to PED to the broader PCS organisation (e.g. to instrument ownership and licensing business, and to the implementation services business) About You Candidates interested this position will have: Advanced degrees and 15+ years of experience in PED research, including COA science, preference research, and regulatory engagement (US FDA essential, EMA and other regulatory agencies desirable) Experience working in a regulatory agency and/or demonstrable track record of developing and executing a COA endpoint strategy with successful outcome of COA label claim Experience preparing for, and participating in Type B and Type C meetings with FDA Experience in developing patient experience materials for regulatory consultations and submissions (e.g. COA dossier, briefing documents for Type B/C/D consultations) An understanding of the global regulatory environment as it pertains to PED Strong scientific consulting skills and track record of contributing to business development in a consulting environment Experience of medical writing for various audiences, including pharmaceutical companies, healthcare professionals, regulatory bodies and patients Publications and recognition in the field through participation in industry consortia or scientific bodies. Experienced public speaker Well-developed written and verbal communication skills including presentations, business and report writing An entrepreneurial nature and interest in developing new client offerings and solutions Demonstrable analytical, interpretative, and problem-solving skills Excellent interpersonal skills and ability to work effectively with others An ability to work in a fast-paced environment with demonstrated ability to effectively manage multiple tasks An ability to establish and maintain effective working relationships in multi-disciplinary and international teams Fluency in English (spoken and written) Willingness and ability to travel from time to time Right to live and work in the recruiting country Physical requirements: Extensive use of telephone communication requiring accurate perception of speech. Extensive use of keyboard requiring repetitive motion of fingers. Regular sitting for extended periods of time. Travel as required. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at
Join us on our exciting journey! IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward. Job Responsibilities - Director, Quality Assurance: Serve as the primary point of contact within Quality and Compliance for triage, evaluation, and routing of all Quality topics pertinent to the supported portfolio. Manage and support routine Quality meetings at all levels of the portfolio, including QA meetings, Joint Operating meetings, Operational Management Meetings, Executive Oversight Committees, and Steering Committees. Provide routine QA metric reporting from the IQVIA Quality Management system, including Quality Issues, Corrective and Preventative Actions, Audits, Inspections, Investigations, and Serious Breaches. Support Quality Issues, Investigations, Serious Breaches (Major & Critical issues), escalations, audits, and inspections impacting the assigned client portfolio. Offer Quality consultation and guidance to IQVIA portfolio teams during routine activities and communicate outcomes and directives from client Quality meetings to IQVIA portfolio operational management. Assist in risk identification and mitigation activities related to portfolio operations and activities, and support portfolio and team Quality initiatives and improvement activities. Lead team improvement initiatives and support team leadership in furthering the service, while recognizing, exemplifying, and adhering to IQVIA's values. Lead, develop, grow, and manage the Quality Management team, ensuring an effective management structure is in place. Ensure that IQVIA QMS procedures are updated to comply with changes in laws, standards, and regulations to accommodate process improvements and business needs. Serve as the RWS expert on Quality-related matters and provide periodic reports on defined key quality indicators to business operations and upper management. In conjunction with the Finance department, prepare the QM department PMA & AIP to ensure effective cost controls. Maintain a current knowledge base through internal and/or external training and participate in professional development through journal articles and by presenting at and attending conferences and professional meetings. Provide input and support to operational teams on issue resolution and process improvement and offer input into Global Quality & Compliance Leadership for strategic direction. Meet with clients and potential clients when necessary and undertake other related duties as assigned. Ensure compliance with all applicable regulatory requirements and standards, develop, and implement regulatory compliance strategies and policies, and monitor changes in regulatory requirements. Conduct internal audits to ensure adherence to regulatory standards, consult with internal regulatory experts, and represent the organization during inspections and audits. Provide training and guidance to staff on regulatory compliance matters, foster a culture of continuous improvement and professional development within the team, and identify and address training needs to enhance team skills and performance. Mentor and coach team members to support their career growth and development, facilitate team-building activities, and conduct regular performance reviews with constructive feedback. Develop and implement risk management strategies to identify, assess, and mitigate potential risks, and monitor and evaluate risk factors that could impact the quality and compliance of the portfolio. Perform risk assessments, create contingency plans, and work with cross-functional teams to incorporate risk management practices into all areas of the portfolio. Develop and implement continuous improvement strategies to enhance quality and efficiency, monitor and analyze quality performance metrics, and lead continuous improvement projects and initiatives. Encourage a culture of innovation and continuous improvement within the team and provide training and support to staff on continuous improvement methodologies and tools. Our Ideal Candidate Will Have: Strong knowledge of Good Clinical Practice (GCP) guidelines. Familiarity with ISO standards, particularly ISO 9001 (Quality Management Systems) and ISO 13485 (Medical Devices). Experience with regulatory compliance and quality management systems (QMS). Proficiency in risk management and continuous improvement methodologies. Excellent leadership and team management skills. Strong analytical and problem-solving abilities. Effective communication and interpersonal skills. Applicants must have the legal right to work in the country they are applying to. Please submit your CV in English! We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
Feb 20, 2025
Full time
Join us on our exciting journey! IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward. Job Responsibilities - Director, Quality Assurance: Serve as the primary point of contact within Quality and Compliance for triage, evaluation, and routing of all Quality topics pertinent to the supported portfolio. Manage and support routine Quality meetings at all levels of the portfolio, including QA meetings, Joint Operating meetings, Operational Management Meetings, Executive Oversight Committees, and Steering Committees. Provide routine QA metric reporting from the IQVIA Quality Management system, including Quality Issues, Corrective and Preventative Actions, Audits, Inspections, Investigations, and Serious Breaches. Support Quality Issues, Investigations, Serious Breaches (Major & Critical issues), escalations, audits, and inspections impacting the assigned client portfolio. Offer Quality consultation and guidance to IQVIA portfolio teams during routine activities and communicate outcomes and directives from client Quality meetings to IQVIA portfolio operational management. Assist in risk identification and mitigation activities related to portfolio operations and activities, and support portfolio and team Quality initiatives and improvement activities. Lead team improvement initiatives and support team leadership in furthering the service, while recognizing, exemplifying, and adhering to IQVIA's values. Lead, develop, grow, and manage the Quality Management team, ensuring an effective management structure is in place. Ensure that IQVIA QMS procedures are updated to comply with changes in laws, standards, and regulations to accommodate process improvements and business needs. Serve as the RWS expert on Quality-related matters and provide periodic reports on defined key quality indicators to business operations and upper management. In conjunction with the Finance department, prepare the QM department PMA & AIP to ensure effective cost controls. Maintain a current knowledge base through internal and/or external training and participate in professional development through journal articles and by presenting at and attending conferences and professional meetings. Provide input and support to operational teams on issue resolution and process improvement and offer input into Global Quality & Compliance Leadership for strategic direction. Meet with clients and potential clients when necessary and undertake other related duties as assigned. Ensure compliance with all applicable regulatory requirements and standards, develop, and implement regulatory compliance strategies and policies, and monitor changes in regulatory requirements. Conduct internal audits to ensure adherence to regulatory standards, consult with internal regulatory experts, and represent the organization during inspections and audits. Provide training and guidance to staff on regulatory compliance matters, foster a culture of continuous improvement and professional development within the team, and identify and address training needs to enhance team skills and performance. Mentor and coach team members to support their career growth and development, facilitate team-building activities, and conduct regular performance reviews with constructive feedback. Develop and implement risk management strategies to identify, assess, and mitigate potential risks, and monitor and evaluate risk factors that could impact the quality and compliance of the portfolio. Perform risk assessments, create contingency plans, and work with cross-functional teams to incorporate risk management practices into all areas of the portfolio. Develop and implement continuous improvement strategies to enhance quality and efficiency, monitor and analyze quality performance metrics, and lead continuous improvement projects and initiatives. Encourage a culture of innovation and continuous improvement within the team and provide training and support to staff on continuous improvement methodologies and tools. Our Ideal Candidate Will Have: Strong knowledge of Good Clinical Practice (GCP) guidelines. Familiarity with ISO standards, particularly ISO 9001 (Quality Management Systems) and ISO 13485 (Medical Devices). Experience with regulatory compliance and quality management systems (QMS). Proficiency in risk management and continuous improvement methodologies. Excellent leadership and team management skills. Strong analytical and problem-solving abilities. Effective communication and interpersonal skills. Applicants must have the legal right to work in the country they are applying to. Please submit your CV in English! We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
Senior Statistical Programmer Global Biostatistics Home-based, office-based, hybrid options available Join us on our exciting journey! The Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability. IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting. We have one of the largest Biostatistics departments within the industry of around 1,100+ staff, to which we engage the full range of industry-leading resources and expertise spanning all study phases and therapeutic areas. Job Overview: As a Senior Statistical Programmer, you will be given access to cutting-edge, in-house technology and opportunities to work on global projects across a variety of therapeutic areas. Thanks to our development opportunities and mentoring at all levels, you will be able to progress your long-term career in the direction you choose. You will provide experienced technical expertise to develop process methodology for the department to meet internal and external clients' needs. You will plan and coordinate the development of integrated programming solutions, serving the full spectrum of statistical programming needs, along with providing technical expertise and leadership to the department and providing internal consulting services, including specifications and user needs analysis for complex project or client requirements. Acting as a lead on studies, you will directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines and support the training of new or junior team members. You will estimate programming scope of work, manage resource assignments, communicate project status, and negotiate/re-negotiate project timelines for deliverables. Requirements: Bachelors or Masters' in Computer Science, Mathematics or equivalent 5+ years Statistical Programming experience within the Life-Science industry Experience in SAS Base, and good knowledge of SAS graph and SAS Macros Excellent knowledge of CDISC standards (SDTM and ADaM) Excellent application development skills Strong understanding of clinical trial data and extremely hands-on in data manipulations, analysis and reporting of analysis results. Experience as technical team lead, directly engaging clients and coordinating tasks within a programming team In-depth knowledge of applicable clinical research regulatory requirements, i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Join IQVIA to see where your skills can take you Global exposure Variety of therapeutic areas Collaborative and supportive team environment Access to cutting-edge and innovative, in-house technology Excellent career development and progression opportunities Work-Life Balance, with a strong focus on a positive well-being Unleash your potential! It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world. When you join our diverse, global team, you'll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.
Feb 17, 2025
Full time
Senior Statistical Programmer Global Biostatistics Home-based, office-based, hybrid options available Join us on our exciting journey! The Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability. IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting. We have one of the largest Biostatistics departments within the industry of around 1,100+ staff, to which we engage the full range of industry-leading resources and expertise spanning all study phases and therapeutic areas. Job Overview: As a Senior Statistical Programmer, you will be given access to cutting-edge, in-house technology and opportunities to work on global projects across a variety of therapeutic areas. Thanks to our development opportunities and mentoring at all levels, you will be able to progress your long-term career in the direction you choose. You will provide experienced technical expertise to develop process methodology for the department to meet internal and external clients' needs. You will plan and coordinate the development of integrated programming solutions, serving the full spectrum of statistical programming needs, along with providing technical expertise and leadership to the department and providing internal consulting services, including specifications and user needs analysis for complex project or client requirements. Acting as a lead on studies, you will directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines and support the training of new or junior team members. You will estimate programming scope of work, manage resource assignments, communicate project status, and negotiate/re-negotiate project timelines for deliverables. Requirements: Bachelors or Masters' in Computer Science, Mathematics or equivalent 5+ years Statistical Programming experience within the Life-Science industry Experience in SAS Base, and good knowledge of SAS graph and SAS Macros Excellent knowledge of CDISC standards (SDTM and ADaM) Excellent application development skills Strong understanding of clinical trial data and extremely hands-on in data manipulations, analysis and reporting of analysis results. Experience as technical team lead, directly engaging clients and coordinating tasks within a programming team In-depth knowledge of applicable clinical research regulatory requirements, i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Join IQVIA to see where your skills can take you Global exposure Variety of therapeutic areas Collaborative and supportive team environment Access to cutting-edge and innovative, in-house technology Excellent career development and progression opportunities Work-Life Balance, with a strong focus on a positive well-being Unleash your potential! It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world. When you join our diverse, global team, you'll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.
Consultant / Senior Consultant Real World Commercial Solutions to Create a Healthier World In RWCS we're passionate about improving the life sciences ecosystem and making decisions that accelerate innovation for a healthier world. Every day our team develops evidence-based strategies that are used in published research, clinical guidelines, and market access decisions, to improve healthcare at every touchpoint. We design and deliver Commercial Analytics, supported by our world-class proprietary data assets, solve complex client challenges through strategic consulting, and use leading edge market research techniques to support clients brand strategy, planning and measurement. We're purpose-driven problem solvers, that do what we love to make a greater impact on human health. The Role In this role, you'll be ensuring on-time and on-budget delivery of completed projects for high client satisfaction. We need insightful, detail-oriented people that can identify and elevate new business opportunities and assist in sales, so we can work with our clients to make a difference in the life science industry. What You'll Be Doing Providing day-to-day client management of projects, including leading update meetings, and participating in delivery workshops. Participation in key aspects of project delivery, such as interview moderation, designing, structuring and delivering client reports and presentations. Leading the definition of research design and planning for proposal purposes. Leadership of extended project teams to execute high quality research across multiple methodologies (RWD, PMR, AIML etc) and analysis on time and within budget. Planning, organising and managing all aspects of project delivery (scope, quality, resources, risk and timelines) to successfully complete specific project goals and objectives. Proactively identifying project related delivery risks and suggesting and implementing mitigating actions. Preparing and facilitating decision making on project related questions, internally as well as with clients. Recommending improvements and alternative solutions to resolve client challenges. Identifying new business opportunities for follow-on work. Supporting business development activities, including proposal writing, pitch development and delivery. Contributing to the EMEA community through networking and cross-team working. Raising the external profile of IQVIA by attending conferences and generating thought leadership pieces. Who You Are A university degree holder with 5-6+ years of experience in life science/healthcare consulting. Previous work experience of at least 6/7 years in consultancy and/or market research. Preferential consideration will be given to candidates with experience in carrying out consulting and market research projects in the pharmaceutical area at an international/cross-country level. Project management experience with client-influencing and relationship-building skills. High skills of interpretation and analysis (quantitative, qualitative and integration of different sources of data assets). Experienced in developing relationships with senior roles at our client organisations. Knowledgeable of developments in the life science industry. Excellent at presenting and communicating. Fluent in English. Benefits We work hard to prioritise the things that matter most to you. Visit our benefits page for information on everything from perks to well-being initiatives and career enhancement.
Feb 13, 2025
Full time
Consultant / Senior Consultant Real World Commercial Solutions to Create a Healthier World In RWCS we're passionate about improving the life sciences ecosystem and making decisions that accelerate innovation for a healthier world. Every day our team develops evidence-based strategies that are used in published research, clinical guidelines, and market access decisions, to improve healthcare at every touchpoint. We design and deliver Commercial Analytics, supported by our world-class proprietary data assets, solve complex client challenges through strategic consulting, and use leading edge market research techniques to support clients brand strategy, planning and measurement. We're purpose-driven problem solvers, that do what we love to make a greater impact on human health. The Role In this role, you'll be ensuring on-time and on-budget delivery of completed projects for high client satisfaction. We need insightful, detail-oriented people that can identify and elevate new business opportunities and assist in sales, so we can work with our clients to make a difference in the life science industry. What You'll Be Doing Providing day-to-day client management of projects, including leading update meetings, and participating in delivery workshops. Participation in key aspects of project delivery, such as interview moderation, designing, structuring and delivering client reports and presentations. Leading the definition of research design and planning for proposal purposes. Leadership of extended project teams to execute high quality research across multiple methodologies (RWD, PMR, AIML etc) and analysis on time and within budget. Planning, organising and managing all aspects of project delivery (scope, quality, resources, risk and timelines) to successfully complete specific project goals and objectives. Proactively identifying project related delivery risks and suggesting and implementing mitigating actions. Preparing and facilitating decision making on project related questions, internally as well as with clients. Recommending improvements and alternative solutions to resolve client challenges. Identifying new business opportunities for follow-on work. Supporting business development activities, including proposal writing, pitch development and delivery. Contributing to the EMEA community through networking and cross-team working. Raising the external profile of IQVIA by attending conferences and generating thought leadership pieces. Who You Are A university degree holder with 5-6+ years of experience in life science/healthcare consulting. Previous work experience of at least 6/7 years in consultancy and/or market research. Preferential consideration will be given to candidates with experience in carrying out consulting and market research projects in the pharmaceutical area at an international/cross-country level. Project management experience with client-influencing and relationship-building skills. High skills of interpretation and analysis (quantitative, qualitative and integration of different sources of data assets). Experienced in developing relationships with senior roles at our client organisations. Knowledgeable of developments in the life science industry. Excellent at presenting and communicating. Fluent in English. Benefits We work hard to prioritise the things that matter most to you. Visit our benefits page for information on everything from perks to well-being initiatives and career enhancement.
Director, Request for Information Job Description IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources, extensive domain expertise and network of partners. IQVIA Connected Intelligence delivers actionable insights and powerful solutions with speed and agility - enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. Request for Information Department The Global Business Operations Request for Information (RFI) Department plays a pivotal role in providing information on IQVIA's capabilities and services that is accurate, reproducible and gives IQVIA a competitive edge. The RFI Department supports the sales process by translating stakeholder questions and developing customer-facing responses from simple questionnaires and eSourcing tool responses through to creating white papers and preferred provider responses to showcase the therapeutic expertise and global capabilities of IQVIA. Purpose Strategic management responsibilities for RFI Department, preparing comprehensive, timely and accurate responses to stakeholders' requests for information to support global sales teams and other internal customers. Responsibilities Manage the RFI Department in accordance with organization's policies and applicable legislation. Responsibilities include planning, assigning, and directing work; appraising performance and guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems. Approve actions on human resources matters, including salary administration. Responsible for performance of direct reports, overseeing large, highly complex RFIs. Responsible for the performance and improvement of corporate information databases and dashboards including the RFI Experience Database, Therapeutic Manage RFI Expertise Database and other relevant tools. Act as the single point of contact for a wide range of customer requests for information across IQVIA, and provide advice and support for high visibility and business critical responses. Development of corporate capabilities and experience documents for strategic proposals, sales initiatives and customer questionnaires. Lead teams of subject matter experts from multiple disciplines and coordinate their inputs to prepare formal replies to customers' global outsourcing and preferred provider request for information (RFIs). Lead improvement initiatives for RFI information processes and procedures. Maintain currency in applicable company management and research databases. Develop processes and manage procedures for company, industry, and competitor research. Perform quality control edits on all documents and work products. Lead the selection and on-boarding process for new RFI staff by conducting candidate review and participating in the interview process. Ensure staff have the appropriate materials, systems access and training to complete job responsibilities. Manage the development and maintenance of department information sources, templates, and related materials. Perform other duties as assigned. Required Knowledge, Skills and Abilities Extensive knowledge of CRO, Pharmaceutical or related industry. Strong motivation and team-building skills. Strong planning and project management skills. Advanced knowledge of Microsoft Excel, PowerPoint and Word. Advanced writing and editing abilities. Excellent communication and organizational skills. Ability to establish and maintain effective working relationships with coworkers, managers and stakeholders. Minimum Required Education and Experience Degree in Life Science, Business Management, Finance, IT or related field. At least 10 year work experience in Proposal and/or Contract Management, Marketing, Finance, IT, Business Management / Development or an equivalent combination of education, training and experience. Physical Requirements Extensive use of telephone and face-to-face communication requiring accurate perception of speech. Extensive use of keyboard requiring repetitive motion of fingers. Grade: 170 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
Feb 09, 2025
Full time
Director, Request for Information Job Description IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources, extensive domain expertise and network of partners. IQVIA Connected Intelligence delivers actionable insights and powerful solutions with speed and agility - enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. Request for Information Department The Global Business Operations Request for Information (RFI) Department plays a pivotal role in providing information on IQVIA's capabilities and services that is accurate, reproducible and gives IQVIA a competitive edge. The RFI Department supports the sales process by translating stakeholder questions and developing customer-facing responses from simple questionnaires and eSourcing tool responses through to creating white papers and preferred provider responses to showcase the therapeutic expertise and global capabilities of IQVIA. Purpose Strategic management responsibilities for RFI Department, preparing comprehensive, timely and accurate responses to stakeholders' requests for information to support global sales teams and other internal customers. Responsibilities Manage the RFI Department in accordance with organization's policies and applicable legislation. Responsibilities include planning, assigning, and directing work; appraising performance and guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems. Approve actions on human resources matters, including salary administration. Responsible for performance of direct reports, overseeing large, highly complex RFIs. Responsible for the performance and improvement of corporate information databases and dashboards including the RFI Experience Database, Therapeutic Manage RFI Expertise Database and other relevant tools. Act as the single point of contact for a wide range of customer requests for information across IQVIA, and provide advice and support for high visibility and business critical responses. Development of corporate capabilities and experience documents for strategic proposals, sales initiatives and customer questionnaires. Lead teams of subject matter experts from multiple disciplines and coordinate their inputs to prepare formal replies to customers' global outsourcing and preferred provider request for information (RFIs). Lead improvement initiatives for RFI information processes and procedures. Maintain currency in applicable company management and research databases. Develop processes and manage procedures for company, industry, and competitor research. Perform quality control edits on all documents and work products. Lead the selection and on-boarding process for new RFI staff by conducting candidate review and participating in the interview process. Ensure staff have the appropriate materials, systems access and training to complete job responsibilities. Manage the development and maintenance of department information sources, templates, and related materials. Perform other duties as assigned. Required Knowledge, Skills and Abilities Extensive knowledge of CRO, Pharmaceutical or related industry. Strong motivation and team-building skills. Strong planning and project management skills. Advanced knowledge of Microsoft Excel, PowerPoint and Word. Advanced writing and editing abilities. Excellent communication and organizational skills. Ability to establish and maintain effective working relationships with coworkers, managers and stakeholders. Minimum Required Education and Experience Degree in Life Science, Business Management, Finance, IT or related field. At least 10 year work experience in Proposal and/or Contract Management, Marketing, Finance, IT, Business Management / Development or an equivalent combination of education, training and experience. Physical Requirements Extensive use of telephone and face-to-face communication requiring accurate perception of speech. Extensive use of keyboard requiring repetitive motion of fingers. Grade: 170 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward. The Patient Centered Solutions team (PCS) The PCS team leads the industry in the science of measuring the patient experience. We pair strategic consulting expertise with technical scientific knowledge to design and execute scientifically rigorous research that incorporates the patient voice into the development and commercialization of new medicines. This research includes qualitative (e.g., patient interviews, focus groups), quantitative (e.g., clinical outcome assessments (COAs)/patient-reported outcomes (PROs), preference research) and passive (e.g., digital health technology tools) approaches to understand patient, caregiver and physician experiences and expectations of disease and treatment. Why join? Become part of a recognized global leader in patient-focused research. Keep growing with an organization that encourages and invests in continuous professional and personal development. Apply your business and leadership skills in an entrepreneurial and multi-disciplinary team. Continue challenging yourself by addressing the toughest client issues, working across multiple geographies and solutions in a dynamic and crucial field for the industry. Make a difference to patients by enabling the successful approval or launch of new treatments with features that are truly patient-centric. Responsibilities As a Principal you will be responsible for maintaining and strengthening relations with current clients as well as for developing business and creating new expansion opportunities for the PCS team. You will assume responsibility for both selling and delivering team projects. Your success will be measured by the ability to lead complex projects, opening up new business relationships to PCS, developing team members and contributing to the development of the PCS function. Develop and deliver insightful, value-added strategies that address complex client issues in the patient science field. Lead sales efforts, including uncovering opportunities, and responding to proposals, to win PCS work. Oversee PCS delivery teams who execute consulting, scientific and analytic projects. Provide direction, advice, and intellectual leadership to clients and delivery teams. Lead PCS services portfolio building and thought leadership initiatives. Identify opportunities for expansion of PCS consulting service offerings. Support the development of the PCS team and global community within IQVIA. Essential experience, skills and education required An advanced degree in a relevant discipline e.g., biological sciences, public health, epidemiology, psychology, sociology, health economics. Strong experience working in roles generating or communicating robust clinical data suitable for submission to regulatory bodies, payers or for publication; preferably with exposure to COA/PRO, patient preference and/or HEOR. Minimum 8 years of experience in healthcare consulting within a Professional Services or CRO business with evidence of career progression. A track record of meeting or exceeding sales targets, managing client/project revenue, leadership and people development. Ability to rapidly understand new scientific content and to engage meaningfully with clients and project teams. Well-developed written and verbal communication skills including presentations, chairing meetings, external conference presentations, workshop facilitation, business and report writing. An entrepreneurial nature and interest in developing new client offerings and solutions and in building the capability to deliver the same. Please submit your CV in English.
Feb 03, 2025
Full time
IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward. The Patient Centered Solutions team (PCS) The PCS team leads the industry in the science of measuring the patient experience. We pair strategic consulting expertise with technical scientific knowledge to design and execute scientifically rigorous research that incorporates the patient voice into the development and commercialization of new medicines. This research includes qualitative (e.g., patient interviews, focus groups), quantitative (e.g., clinical outcome assessments (COAs)/patient-reported outcomes (PROs), preference research) and passive (e.g., digital health technology tools) approaches to understand patient, caregiver and physician experiences and expectations of disease and treatment. Why join? Become part of a recognized global leader in patient-focused research. Keep growing with an organization that encourages and invests in continuous professional and personal development. Apply your business and leadership skills in an entrepreneurial and multi-disciplinary team. Continue challenging yourself by addressing the toughest client issues, working across multiple geographies and solutions in a dynamic and crucial field for the industry. Make a difference to patients by enabling the successful approval or launch of new treatments with features that are truly patient-centric. Responsibilities As a Principal you will be responsible for maintaining and strengthening relations with current clients as well as for developing business and creating new expansion opportunities for the PCS team. You will assume responsibility for both selling and delivering team projects. Your success will be measured by the ability to lead complex projects, opening up new business relationships to PCS, developing team members and contributing to the development of the PCS function. Develop and deliver insightful, value-added strategies that address complex client issues in the patient science field. Lead sales efforts, including uncovering opportunities, and responding to proposals, to win PCS work. Oversee PCS delivery teams who execute consulting, scientific and analytic projects. Provide direction, advice, and intellectual leadership to clients and delivery teams. Lead PCS services portfolio building and thought leadership initiatives. Identify opportunities for expansion of PCS consulting service offerings. Support the development of the PCS team and global community within IQVIA. Essential experience, skills and education required An advanced degree in a relevant discipline e.g., biological sciences, public health, epidemiology, psychology, sociology, health economics. Strong experience working in roles generating or communicating robust clinical data suitable for submission to regulatory bodies, payers or for publication; preferably with exposure to COA/PRO, patient preference and/or HEOR. Minimum 8 years of experience in healthcare consulting within a Professional Services or CRO business with evidence of career progression. A track record of meeting or exceeding sales targets, managing client/project revenue, leadership and people development. Ability to rapidly understand new scientific content and to engage meaningfully with clients and project teams. Well-developed written and verbal communication skills including presentations, chairing meetings, external conference presentations, workshop facilitation, business and report writing. An entrepreneurial nature and interest in developing new client offerings and solutions and in building the capability to deliver the same. Please submit your CV in English.
Director, Pharmacokinetics Home-Based/Hybrid: Europe/UK Decision Sciences - Clinical Pharmacology/Pharmacokinetics Job Profile Summary Perform analysis and reporting of Phase I-IV clinical pharmacology studies, such as dose tolerance, dose proportionality, mass balance, concept testing, bioavailability, thorough QTc, drug-drug interactions, and special population (age effects, renal disease, hepatic disease, gender effects, etc.), as well as population PK/PD studies. Provide consulting on study design, or other aspects of Clinical Pharmacology projects, clinical development plans, and dossiers for product registration. Assist Clinical Pharmacology management in implementing strategic initiatives. Responsibilities As a project PK Scientist develop or oversee the development of protocols, statistical analysis plans, PK/PD analysis, PK/PD tables, listings and figures, and clinical study reports for Phase I-IV clinical pharmacology studies, such as dose tolerance, dose proportionality, mass balance, concept testing, bioavailability, thorough QTc, drug-drug interactions, and special population (age effects, renal disease, hepatic disease, gender effects, etc.), as well as population PK/PD studies. Consult with clients, external IQVIA divisions, and Clinical Pharmacology staff on study design, or other aspects of Clinical Pharmacology projects, and clinical development plans. Prepare PK/PD sections of global dossiers for product registration and communicate with local regulatory agencies. Ensure quality and timely delivery of the project PK/PD deliverables to IQVIA clients. Provide update to the IQVIA Project Manager on status of project PK/PD deliverables. Participate on project-related cross functional teams that include Project Manager, CRA, Data Manager, Biostatistician, Programmer, and/or Medical Writer. Consult and interact with clients, other IQVIA divisions, and third-party vendors. Provide technical training, guidance, and mentorship to lower level and new staff. Participate in proposal and budget development for Clinical Pharmacology PK/PD components of business proposals. Recommend and assist in implementation of quality control (QC) assessment and procedures and scientific review. Assist management in implementing strategic initiatives. Maintain awareness of overall developments in the field of Clinical Pharmacology and PK/PD based on current literature, application of new technology, attendance at professional meetings, etc. Perform other duties as assigned by Clinical Pharmacology Management. MINIMUM REQUIRED EDUCATION AND EXPERIENCE Experience 7 - 10 years of prior relevant experience. Education Ph.D. or educational equivalent in Pharmacokinetics, Pharmaceutics, or related field, or Master's Degree or PharmD in Pharmacy or related field Skills and Abilities Sound knowledge of Pharmacokinetic concepts, including noncompartmental analysis and population PK modeling as required, current therapeutic environment and drug development trends Sound knowledge of appropriate PK/PD standards and processes Strong understanding of the principles of the drug development process, ICH GCP, and applicable International and national regulatory requirements Good coaching and mentoring skills Good problem solving and analytical skills Excellent computer skills, including proficiency with Microsoft Office, WinNonlin, Excellent verbal and written communication skills and highly effective interpersonal, and organizational skills Ability to work within a matrix team environment Ability to prioritize, and independently coordinate and manage PK/PD component of complex projects Ability to interact in a cross-functional and multi-cultural team environment Ability to establish and maintain effective working relationships with coworkers, managers and clients JOIN US! Embrace your curiosity and grow your career in an exciting environment where development is a priority. Think boldly and disrupt conventional thinking. Enjoy what you do! IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at
Dec 18, 2022
Full time
Director, Pharmacokinetics Home-Based/Hybrid: Europe/UK Decision Sciences - Clinical Pharmacology/Pharmacokinetics Job Profile Summary Perform analysis and reporting of Phase I-IV clinical pharmacology studies, such as dose tolerance, dose proportionality, mass balance, concept testing, bioavailability, thorough QTc, drug-drug interactions, and special population (age effects, renal disease, hepatic disease, gender effects, etc.), as well as population PK/PD studies. Provide consulting on study design, or other aspects of Clinical Pharmacology projects, clinical development plans, and dossiers for product registration. Assist Clinical Pharmacology management in implementing strategic initiatives. Responsibilities As a project PK Scientist develop or oversee the development of protocols, statistical analysis plans, PK/PD analysis, PK/PD tables, listings and figures, and clinical study reports for Phase I-IV clinical pharmacology studies, such as dose tolerance, dose proportionality, mass balance, concept testing, bioavailability, thorough QTc, drug-drug interactions, and special population (age effects, renal disease, hepatic disease, gender effects, etc.), as well as population PK/PD studies. Consult with clients, external IQVIA divisions, and Clinical Pharmacology staff on study design, or other aspects of Clinical Pharmacology projects, and clinical development plans. Prepare PK/PD sections of global dossiers for product registration and communicate with local regulatory agencies. Ensure quality and timely delivery of the project PK/PD deliverables to IQVIA clients. Provide update to the IQVIA Project Manager on status of project PK/PD deliverables. Participate on project-related cross functional teams that include Project Manager, CRA, Data Manager, Biostatistician, Programmer, and/or Medical Writer. Consult and interact with clients, other IQVIA divisions, and third-party vendors. Provide technical training, guidance, and mentorship to lower level and new staff. Participate in proposal and budget development for Clinical Pharmacology PK/PD components of business proposals. Recommend and assist in implementation of quality control (QC) assessment and procedures and scientific review. Assist management in implementing strategic initiatives. Maintain awareness of overall developments in the field of Clinical Pharmacology and PK/PD based on current literature, application of new technology, attendance at professional meetings, etc. Perform other duties as assigned by Clinical Pharmacology Management. MINIMUM REQUIRED EDUCATION AND EXPERIENCE Experience 7 - 10 years of prior relevant experience. Education Ph.D. or educational equivalent in Pharmacokinetics, Pharmaceutics, or related field, or Master's Degree or PharmD in Pharmacy or related field Skills and Abilities Sound knowledge of Pharmacokinetic concepts, including noncompartmental analysis and population PK modeling as required, current therapeutic environment and drug development trends Sound knowledge of appropriate PK/PD standards and processes Strong understanding of the principles of the drug development process, ICH GCP, and applicable International and national regulatory requirements Good coaching and mentoring skills Good problem solving and analytical skills Excellent computer skills, including proficiency with Microsoft Office, WinNonlin, Excellent verbal and written communication skills and highly effective interpersonal, and organizational skills Ability to work within a matrix team environment Ability to prioritize, and independently coordinate and manage PK/PD component of complex projects Ability to interact in a cross-functional and multi-cultural team environment Ability to establish and maintain effective working relationships with coworkers, managers and clients JOIN US! Embrace your curiosity and grow your career in an exciting environment where development is a priority. Think boldly and disrupt conventional thinking. Enjoy what you do! IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at
We are looking for a dedicated Director, Site Solutions, to be part of the Clinical Trial Payments department. Essential Functions: • Create and manage strategic relationships and alliances with assigned customer; build networks with necessary stakeholders internally and externally. • As it pertains to DSSR, collaborate in the definition of customer-centric, account management strategies and provide oversight of their implementation within assigned account(s) i.e. solicitation of repeat business; identification of new business opportunities developing to RFPs; assist in contribution of customer centric, strategic focus to proposal development process; assist in transforming customer relationships to partnership level; establish mutually agreed working practices with customer for standardization implementation across projects/programs; contribute to strategic planning, assist in creative solutions and ongoing process improvements to meet anticipated future customer needs; provide customer feedback; status reports. • Work with DSSR operational leaders and customer stakeholders to develop, implement and track key performance indicators (KPIs) and develop timelines and processes for tracking KPIs on an account/portfolio level. • Provide Senior Level oversight and/or act as an Account Owner for a customer alliance, by partnering with other DSSR functional leads to develop and implement process improvements, to ensure consistency, provide oversight of portfolio level quality and financial metrics, etc. • Oversee the scope of work, objectives, timelines, quality of deliverables, and other activities for assigned clients and associated programs as it pertains to DSSR • Act as the key relationship manager and primary contact for DSSR to assigned client contacts to ensure appropriate communication channels are maintained as well as recommend courses of action regarding client management issues. • Collaborate with other IQVIA alliance managers, BD personnel and customer managers to present a single voice and strategy to the customer. • Lead internal DSSR escalation meetings to ensure quick response to any quality concerns or customer escalations, ensuring appropriate representatives from stakeholders and operational management are involved as appropriate. • Accountable for leading the development of account specific strategies that align operations, sales and corporate development within DSSR with that of the customer. • Review and oversee program budget(s) to meet financial and company goals proactively ensure adherence to change control processes. • Oversee and support complex, global contracts which govern functional service providership, project units, managed partnerships, and/or risk shared investments to the customer's satisfaction. • Leads global departmental initiatives for DSSR focused on enhancing customer delivery, creating new offerings, developing new systems or tools to enhance oversight, etc. • Represent assigned client to internal stakeholders; provide consultation to clients on strategy and operational delivery as needed; serve as an internal consultant to other DSSR business partners for integrated functional solutions • Participate in market research and competitive analysis activities that provide information in support of the business needs analysis process and strategic account management. • Provide effective senior representation of DSSR in high visibility forums e.g. joint IQVIA Committees, Joint Operations Teams, etc. representing IQVIA with the highest level of professionalism. Expecting qualification: • Bachelor's Degree Life Science, Business Management or related field • 12 years in the pharmaceutical, CRO, or related industry, experience to include clinical operations, CRA, Commercial and /or alternative operational functional (e.g. business development, data management, project management, laboratory, pre-clinical) Join us on our exciting journey! IQVIA is The Human Data Science Company , focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human ingenuity to drive healthcare forward. We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and Whatever your career goals, we are here to ensure you get there! IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at
Dec 10, 2022
Full time
We are looking for a dedicated Director, Site Solutions, to be part of the Clinical Trial Payments department. Essential Functions: • Create and manage strategic relationships and alliances with assigned customer; build networks with necessary stakeholders internally and externally. • As it pertains to DSSR, collaborate in the definition of customer-centric, account management strategies and provide oversight of their implementation within assigned account(s) i.e. solicitation of repeat business; identification of new business opportunities developing to RFPs; assist in contribution of customer centric, strategic focus to proposal development process; assist in transforming customer relationships to partnership level; establish mutually agreed working practices with customer for standardization implementation across projects/programs; contribute to strategic planning, assist in creative solutions and ongoing process improvements to meet anticipated future customer needs; provide customer feedback; status reports. • Work with DSSR operational leaders and customer stakeholders to develop, implement and track key performance indicators (KPIs) and develop timelines and processes for tracking KPIs on an account/portfolio level. • Provide Senior Level oversight and/or act as an Account Owner for a customer alliance, by partnering with other DSSR functional leads to develop and implement process improvements, to ensure consistency, provide oversight of portfolio level quality and financial metrics, etc. • Oversee the scope of work, objectives, timelines, quality of deliverables, and other activities for assigned clients and associated programs as it pertains to DSSR • Act as the key relationship manager and primary contact for DSSR to assigned client contacts to ensure appropriate communication channels are maintained as well as recommend courses of action regarding client management issues. • Collaborate with other IQVIA alliance managers, BD personnel and customer managers to present a single voice and strategy to the customer. • Lead internal DSSR escalation meetings to ensure quick response to any quality concerns or customer escalations, ensuring appropriate representatives from stakeholders and operational management are involved as appropriate. • Accountable for leading the development of account specific strategies that align operations, sales and corporate development within DSSR with that of the customer. • Review and oversee program budget(s) to meet financial and company goals proactively ensure adherence to change control processes. • Oversee and support complex, global contracts which govern functional service providership, project units, managed partnerships, and/or risk shared investments to the customer's satisfaction. • Leads global departmental initiatives for DSSR focused on enhancing customer delivery, creating new offerings, developing new systems or tools to enhance oversight, etc. • Represent assigned client to internal stakeholders; provide consultation to clients on strategy and operational delivery as needed; serve as an internal consultant to other DSSR business partners for integrated functional solutions • Participate in market research and competitive analysis activities that provide information in support of the business needs analysis process and strategic account management. • Provide effective senior representation of DSSR in high visibility forums e.g. joint IQVIA Committees, Joint Operations Teams, etc. representing IQVIA with the highest level of professionalism. Expecting qualification: • Bachelor's Degree Life Science, Business Management or related field • 12 years in the pharmaceutical, CRO, or related industry, experience to include clinical operations, CRA, Commercial and /or alternative operational functional (e.g. business development, data management, project management, laboratory, pre-clinical) Join us on our exciting journey! IQVIA is The Human Data Science Company , focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human ingenuity to drive healthcare forward. We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and Whatever your career goals, we are here to ensure you get there! IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at
Join us on our exciting journey! IQVIA is The Human Data Science Company , focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human ingenuity to drive healthcare forward. JOB OVERVIEW AND ROLE PURPOSE • This is a prominent client facing role in the Global MedTech Device Consulting Center of Excellence • You work with clients, IQVIA consulting peers and IQVIA account management to provide value added input as a trusted advisor • You generate and close commercial consulting opportunities that lead to additional starbursts (this includes but is not limited to MedTech-specific market access, go-to-market strategy, commercial excellence, market landscaping and other project types) • You meet or exceed assigned revenue targets • In addition, you: Drive sales of consulting services (incl. market research, market access, strategy, commercial excellence engagements) to MedTech clients globally Lead proposal development and oversee project delivery to ensure highest client satisfaction RESPONSIBILITIES Sales leadership: • Achieves or exceeds individual annual revenue targets for commercial consulting projects • Seeks out and identifies new revenue opportunities at existing and potential clients - ensures a continuous flow of business from client engagements • Takes on a lead role in proposal development to ensure actionable, on-target and timely proposals are provided to clients • Manages client interface and ensures project team achieves efficient and effective project delivery • Serves as a solutions-based expert (ideally in a MedTech-related field), internally and externally, by applying consultative problem-solving skills • Identifies issues of importance to the industry/clients and works with CoE Leaders and/or Geographic Leaders to develop tangible commercial offerings • Contributes to the enhanced awareness of IQVIA in the marketplace, e.g. through speaking engagements, client meetings, publications etc. • Proactively continues to strengthen subject matter expertise through on the job experience, participation in conferences and symposiums and other forums for professional knowledge sharing • Proactively mentors, coaches and shares subject matter expertise with others to elevate our capabilities to deliver world-class solutions for clients Engagement management and project oversight: • Primary owner of client engagements with the responsibility for client satisfaction and delivering high levels of quality/added value • Manage client interface and oversee international project teams to achieve efficient, effective, and timely project delivery OUR IDEAL CANDIDATE WILL HAVE • Degree in Life Science, Engineering, Medical or a related field • Typically requires 10+ years of professional experience incl. management / strategy consulting • Deep knowledge of the MedTech or adjacent sectors • In depth and long-standing relationships with client companies, especially at a senior level • Proven success in sales of professional services • Proven ability to build trusted partnership with clients • Hands-on knowledge of consulting methods & market research • Values people's opinions and encourages knowledge sharing and team spirit • Fluency in English; additional language(s) a plus • Ability to quickly build relationships and network (clients, colleagues) • Excellent written and verbal communication skills • Proactive, self-motivated, can manage own workload with minimal direction • Positive, energetic, flexible, 'can do' attitude • A solution focused mindset • Excited about bringing cutting-edge data and technology into commercial consulting • Ability to interpret and present complex concepts • Able to work collaboratively in complex matrix teams & structures • Proven ability to manage multiple clients effectively • Ability to profitably price engagements • Comfortable with significant virtual working • High proficiency in of Microsoft PowerPoint, Excel, Word, Outlook, Teams • Easy access to an airport to travel within Europe We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA . IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at
Nov 29, 2022
Full time
Join us on our exciting journey! IQVIA is The Human Data Science Company , focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human ingenuity to drive healthcare forward. JOB OVERVIEW AND ROLE PURPOSE • This is a prominent client facing role in the Global MedTech Device Consulting Center of Excellence • You work with clients, IQVIA consulting peers and IQVIA account management to provide value added input as a trusted advisor • You generate and close commercial consulting opportunities that lead to additional starbursts (this includes but is not limited to MedTech-specific market access, go-to-market strategy, commercial excellence, market landscaping and other project types) • You meet or exceed assigned revenue targets • In addition, you: Drive sales of consulting services (incl. market research, market access, strategy, commercial excellence engagements) to MedTech clients globally Lead proposal development and oversee project delivery to ensure highest client satisfaction RESPONSIBILITIES Sales leadership: • Achieves or exceeds individual annual revenue targets for commercial consulting projects • Seeks out and identifies new revenue opportunities at existing and potential clients - ensures a continuous flow of business from client engagements • Takes on a lead role in proposal development to ensure actionable, on-target and timely proposals are provided to clients • Manages client interface and ensures project team achieves efficient and effective project delivery • Serves as a solutions-based expert (ideally in a MedTech-related field), internally and externally, by applying consultative problem-solving skills • Identifies issues of importance to the industry/clients and works with CoE Leaders and/or Geographic Leaders to develop tangible commercial offerings • Contributes to the enhanced awareness of IQVIA in the marketplace, e.g. through speaking engagements, client meetings, publications etc. • Proactively continues to strengthen subject matter expertise through on the job experience, participation in conferences and symposiums and other forums for professional knowledge sharing • Proactively mentors, coaches and shares subject matter expertise with others to elevate our capabilities to deliver world-class solutions for clients Engagement management and project oversight: • Primary owner of client engagements with the responsibility for client satisfaction and delivering high levels of quality/added value • Manage client interface and oversee international project teams to achieve efficient, effective, and timely project delivery OUR IDEAL CANDIDATE WILL HAVE • Degree in Life Science, Engineering, Medical or a related field • Typically requires 10+ years of professional experience incl. management / strategy consulting • Deep knowledge of the MedTech or adjacent sectors • In depth and long-standing relationships with client companies, especially at a senior level • Proven success in sales of professional services • Proven ability to build trusted partnership with clients • Hands-on knowledge of consulting methods & market research • Values people's opinions and encourages knowledge sharing and team spirit • Fluency in English; additional language(s) a plus • Ability to quickly build relationships and network (clients, colleagues) • Excellent written and verbal communication skills • Proactive, self-motivated, can manage own workload with minimal direction • Positive, energetic, flexible, 'can do' attitude • A solution focused mindset • Excited about bringing cutting-edge data and technology into commercial consulting • Ability to interpret and present complex concepts • Able to work collaboratively in complex matrix teams & structures • Proven ability to manage multiple clients effectively • Ability to profitably price engagements • Comfortable with significant virtual working • High proficiency in of Microsoft PowerPoint, Excel, Word, Outlook, Teams • Easy access to an airport to travel within Europe We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA . IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at