IQVIA LLC

IQVIA LLC is seeking a Clinical Data Management Lead to oversee data management for global clinical trials. This fully remote role offers the opportunity to mentor junior staff and oversee compliance while managing large global studies. Ideal candidates will have at least 10 years of experience in clinical data management, including a leadership role. The position offers competitive salary and performance-based incentives, fostering a culture of growth and collaboration.

Job Overview IQVIA is growing and hiring multiple Clinical Data Management (CDM) Leads across our Functional Service Provider and traditional delivery models. The role is a remote/WFH position with all necessary equipment provided. Responsibilities Lead data management for complex, global clinical trials from study setup to database lock. Serve as the main client contact for all data management deliverables. Oversee SAE, PK, and external data reconciliation and database deployment. Manage timelines, budgets, and resource allocation to meet customer expectations. Mentor junior data management staff and promote best practices. Drive process improvements and ensure regulatory and SOP compliance. Qualifications Bachelor's degree in life sciences, health, clinical, biological, or mathematical field. No less than 10 years of direct clinical data management experience, with 5+ years in a Lead Clinical Data Management role. Previous roles may include Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager. Proven success managing large global studies (1000+ patients). Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. Strong understanding of GCP, ICH, and clinical research processes. Excellent communication and leadership skills. What IQVIA Offers Fully remote role - company equipment provided. Competitive salary and performance-based incentives. Career growth and learning opportunities through mentoring and internal mobility. Inclusive, global culture focused on innovation and collaboration.

IQVIA is seeking a Senior Statistical Programmer (FSP) to operate from a home-based setup across multiple locations in Europe. You will design, develop and QA SAS programs for submission-ready datasets and analyze complex clinical data in CDISC ADaM format. Key responsibilities include leading analysis activities, delivering Tables, Figures and Listings, and coordinating with statistics teams and CROs to ensure regulatory submission readiness.

IQVIA LLC is seeking an experienced Virtual Key Account Manager to support a smoking cessation portfolio across UK healthcare accounts. The role focuses on virtual engagement with GPs, community pharmacists, public health and integrated care systems to drive awareness, adoption and growth. Excellent opportunity for an autonomous professional with ABPI credentials and NHS insight to join a national remote team.

AI Consultant - Principal page is loaded AI Consultant - Principallocations: London, United Kingdom: Paris, Francetime type: Full timeposted on: Posted Todayjob requisition id: R Join a Ground Breaking AI Initiative at IQVIA IQVIA is building a world class team to develop large scale AI solutions using cutting edge machine learning architectures. Our mission is to integrate data across clinical, real world, and biomedical sources to unlock new insights into patient trajectories-and transform how we understand and anticipate health outcomes. About the Role We are seeking a Director or Principal level Consultant to lead the selling and delivery of cutting edge AI projects in the Life Sciences R&D space, with a key focus on Clinical Development Optimization.This high impact, client facing role requires someone who can craft strategic AI roadmaps while also guiding technical solution delivery alongside data scientists and engineers. You will play a pivotal role in shaping a new practice, growing a team, and influencing the future of AI in Pharma R&D. Key Responsibilities Client Engagement & Business Development Lead the full sales cycle: opportunity identification, proposals, client presentations, and deal closure. Act as a trusted advisor to senior stakeholders across Pharma and Life Sciences. Identify and cultivate new opportunities across Clinical R&D. Sell first in class AI solutions, including offerings still in development that require co creation with clients. Develop compelling narratives around IQVIA's newest AI solutions and systems. Project Leadership & Delivery Design and oversee delivery of AI/ML projects involving clinical development simulation, RWD, trial data, omics, and other structured/unstructured sources. Manage cross functional teams to ensure high quality, on time delivery and client satisfaction. Support development of next generation foundation model initiatives. Design, develop, deploy, and evangelize scalable, high performance AI solutions using state of the art platforms. Lead multidisciplinary teams combining industry, technical, and functional expertise. Guide development of AI strategy roadmaps, PoCs, ML pipelines, and deployment strategies. Collaborate with external technology partners for successful delivery. Practice Building Shape and scale a new AI Life Sciences practice, including defining offerings and mentoring new team members. Contribute to thought leadership (white papers, conferences, workshops). Foster an agile, innovative, impact driven team culture. Ideal Candidate Profile Must Haves 5-10+ years in Consulting with focus on AI, Data Science, or Digital Transformation. Experience in both business development and delivery of complex AI/ML projects. Strong understanding of AI/ML techniques (supervised, unsupervised, generative AI, LLMs, agentic AI). Domain expertise in Life Sciences-ideally Pharma R&D, Clinical Trials, or Clinical Operations. Demonstrated ability to manage senior client relationships as a strategic advisor. Leadership experience managing consultants, data scientists, and technical teams. Proven ability to conceive, sell, and deliver novel solutions. Strong drive, ownership, and execution mindset. Nice to Haves Experience at a top tier consulting firm. Understanding of regulatory and governance frameworks (HIPAA, 21 CFR Part 11). Exposure to RWE, biomarker discovery, or trial optimization. Experience with agentic AI or LLM orchestration in Life Sciences. Familiarity with platforms such as AWS, Azure ML, Databricks, foundation model platforms (e.g., ChatGPT, Claude), or modern code/AI tooling. What We're Looking For Polymath mindset: Ability to combine strategy, technical depth, and stakeholder influence. Entrepreneurial drive: Motivation to build a new capability, team, and practice. Creative problem solver: Ability to execute under ambiguity with a "jugaad" spirit. Mission orientation: A genuine desire to transform how medicines are discovered and developed. What We Offer Opportunity to lead and shape a high growth business unit at the forefront of AI in Life Sciences. Autonomy, flexibility, and strong support for innovation. A mission driven team passionate about transforming healthcare through AI.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 atIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

A leading provider in Life Sciences seeks an experienced AI Consultant - Principal to lead AI project delivery and business development. The ideal candidate will have 5-10 years of consulting experience with a strong focus on AI and Data Science. Responsibilities include overseeing AI/ML projects and shaping a new practice within Life Sciences. This role requires excellent client management skills and a disruptive mindset to drive innovation in Pharma R&D.

Business Development Manager - Medical Affairs Solutions (IQVIA Pharma Review)Applylocations: London, United Kingdom: Madrid, Spain: Barcelona, Spain: Reading, Berkshire, United Kingdomtime type: Full timeposted on: Posted 8 Days Agojob requisition id: R Join us on our exciting journey! IQVIATM is The Human Data Science CompanyTM, 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. Business Development Manager - Medical Affairs Solutions (IQVIA Pharma Review) IQVIA Pharma Review specializes in delivering high quality scientific content solutions that support pharma and biotech teams across the product lifecycle. With deep expertise in scientific review and approval, Pharma Review enables organizations to accelerate the review and approval of clear, accurate, and compliant scientific materials.Leveraging IQVIA's global data assets, technology platforms, and advanced analytics, we provide an integrated approach to scientific content creation, ensuring consistency, efficiency, and scientific rigor. Our teams combine therapeutic area expertise with streamlined processes to deliver timely, high impact outputs that support strategic decision making and enhance scientific engagement.We empower life sciences organizations to operate with greater agility and maintain the highest scientific quality standards. Responsibilities As a Business Development Manager, you will drive the growth of Pharma Review's scientific content solutions business. Working closely with pharmaceutical and biotech clients, you will help identify opportunities where medical review, and content development services can address critical business needs. You will act as a trusted partner to clients, translating their scientific communication challenges into tailored Pharmareview solutions. Scientific Content Solutions & Business Development Drive business growth for Pharma Review's scientific content and medical review and approval offerings Engage with pharmaceutical and biotech clients to understand their scientific communication, publication, and content development needs Position Pharma review's capabilities to prospective and existing clients Work with scientific and operational teams to develop tailored solutions aligned to client objectives Identify opportunities to expand existing client relationships and support new business acquisition Client Engagement & Solution Development Develop value propositions that demonstrate the impact of high-quality scientific content on client objectives Support proposal development, client presentations, and commercial discussions Collaborate with subject matter experts to create compelling solution narratives and case studies Gather market intelligence and customer feedback to support the evolution of Pharmareview's service offerings Go-to-Market & Thought Leadership Support the development of sales collateral, client-facing content, and business development materials Promote awareness of Pharma Review capabilities across IQVIA commercial teams Contribute to thought leadership activities focused on scientific communications, medical writing, publications, and content innovation Represent Pharma Review at industry conferences and client meetings, as appropriate Requirements 5+ years of experience in business development, account management, medical communications, scientific services, or related commercial roles within life sciences Strong understanding of scientific communications, medical writing, publications, medical review processes, and content development Experience engaging with pharmaceutical and biotech stakeholders Commercial mindset with a proven ability to identify and develop business opportunities Ability to translate client needs into tailored scientific content solutions Excellent communication, presentation, and stakeholder management skills Experience working in medical communications agencies, scientific content organizations, CROs, or related service providers is highly desirable Deep knowledge of review and approval process, and relevant codes (EFPIA, ABPI) Familiarity with AI-enabled content creation, content operations, or digital scientific communications is advantageous Why Join? Those who join us become part of a recognized global leader still willing to challenge the status quo to improve patient care. You will have access to the most cutting-edge technology, the largest data sets, the best analytics tools and, in our opinion, some of the finest minds in the Healthcare industry.You can drive your career at IQVIA and choose the path that best defines your development and success. With exposure across diverse geographies, capabilities, and vast therapeutic and information and technology areas, you can seek opportunities to change and grow without boundaries.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 ultimately improve human health outcomes.It's an exciting time to join and reimagine what's possible in healthcare. Moving healthcare forward. Together. IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential. 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 is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA LLC is seeking an experienced Virtual Key Account Manager to work on priority accounts in Reading, UK. This role involves maximizing opportunities and working collaboratively with stakeholders. The ideal candidate will have a successful negotiation background, pharmaceutical sales experience, and a relevant degree. A competitive salary, bonus scheme, and comprehensive benefits are offered, including private healthcare and flexible working options.

IQVIA LLC is seeking a Senior Clinical Editor to conduct quality control reviews of Medical Writing deliverables at our London location. The role requires strong leadership in managing QC tasks and training staff, with a focus on accuracy and compliance. The ideal candidate will have a Bachelor's or higher in a life sciences discipline, at least 8 years of experience in clinical trial documentation, and a keen eye for detail in English-language documents.

Senior Clinical EditorApplylocations: London, United Kingdom: Vienna, Austria: Brussels, Brussels-Capital Region, Belgium: Barcelona, Spain: Amsterdam, Netherlandstime type: Full timeposted on: Posted 8 Days Agojob requisition id: R Job Overview Performs quality control review of Medical Writing deliverables from internal and external authors to ensure accuracy, consistency, and compliance with format and style requirements. Provides leadership, training, and guidance to staff, and assists in resource management. Essential Functions Is a subject matter expert within the group and a source of advice and information to IQVIA staff on quality control processes; Conduct quality control (QC) review of a wide range of Medical Writing deliverables for both internal and external customers, including complex and substantial documents, with limited guidance and consistent high quality and efficiency; Document findings clearly, in accordance with defined procedures and checklists; Liaise promptly with document authors in case of questions or missing sources; Provide service metrics and scores, as required; Develop quality tools such as checklists, quality guidelines, standards and scoring methodology to meet project specific needs; May have responsibility for resourcing of QC tasks within the team; Take a leading role in providing training, guidance, and mentoring within the QC group; May take a formal supervisory role in managing QC staff and/or contract resources; Take a leading role in proposing, developing, evaluating, and implementing process changes and tools and monitoring their adoption and benefits; Take a leading role in QC team meetings and ensuring that lessons learned are shared and consistent approaches are applied; Contribute to budget proposals for QC tasks and maintain a clear understanding of the time and resources needed for tasks within remit; May take a leadership role for a stand-alone QC project, lead the team, and be the primary contact with the customer; May participate in project team meetings and liaise directly with the customer on QC issues, as appropriate and with senior support as needed; Take responsibility for on-time delivery of QC review comments; Manage daily assignments, planning and directing work, and take responsibility for managing workload for assigned projects and tasks, in collaboration with senior staff; Keep abreast of current data, trends, medical writing (MW)/regulatory knowledge, developments and advances in area of drug development/MW. Qualifications Bachelor's Degree Life sciences related discipline or related field Req Master's Degree Life sciences related discipline or related field Pref Ph.D. Life sciences related discipline or related field Pref Typically, at least 8 years experience working with clinical trial documentation in a research environment, including significant experience of performing quality control (QC) review of clinical trial-related documents, defining and refining processes, and training and developing others. Experience Requires in-depth understanding of the structure, format, and purpose of a wide range of MW deliverables and the importance of consistency, clarity, and accuracy versus sources. Req Careful attention to detail, accuracy, and consistency; Impeccable English language skills and ability to detect and correct grammatical, spelling, and language errors; Ability to understand scientific/medical documents and identify deficiencies, errors and inconsistencies; Familiarity with the structural and content requirements of clinical study reports, protocols, and similar documents; Proactivity and advanced organizational and time management skills and ability to prioritize workload effectively with commitment to deadlines; Ability to communicate clearly, concisely, and effectively in English, both in writing and verbally, and confidence in using a range of communication methods to achieve results; Good understanding of clinical drug development and the functions, steps, and processes involved; Advanced understanding of the nature and purpose of Medical Writing deliverables; Ability to provide clear and effective guidance and training in the form of written instructions, presentations, and one-to-one discussion; Ability to provide thorough, appropriate, and sensitive feedback to less experienced colleagues; Confident use of Microsoft Office and Adobe Acrobat; Ability to quickly establish and maintain effective working relationships with co-workers, managers, and customers at a range of seniority levels.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 is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.