IQVIA LLC

IQVIA LLC is looking for a Senior Data Scientist to join our Data Science, Analytics, and Technology Solutions team in Brighton, UK. This role will be crucial in designing and maintaining healthcare data solutions using the OHDSI and DARWIN frameworks. Candidates should have proven experience with the OMOP Common Data Model, SQL, R, and Python. The position offers opportunities to work within a leading pharmaceutical environment, contributing directly to real-world evidence projects.

Senior Data Scientist (Data Science, Analytics, and Technology Solutions (DATS Brighton, UK IQVIA is hiring to expand our dedicated Real World Evidence (RWE) FSP team, working fully embedded within the environment of a leading pharmaceutical client. This Data Scientist role sits within our Data Science, Analytics, and Technology Solutions (DATS) team and will play a key role in designing, implementing, and maintaining healthcare data solutions using the OHDSI and DARWIN frameworks. Essential Functions Collaborate with researchers and data scientists to understand project requirements and translate them into OHDSI/DARWIN compatible solutions. Work with databases, ensuring data integrity and optimization for OHDSI related queries and analyses. Perform data analyses in OHDSI related tools like ATLAS and Prometheus or using R packages. Customize and extend OHDSI tools and applications to meet specific project needs. Collaborate with cross functional teams to troubleshoot and resolve technical issues related to OHDSI implementations. Stay informed about OHDSI community updates, best practices, and emerging trends in observational health data research. Support the growth and maintenance of the OHDSI community on the client side. Requirements Proven experience with the Observational Medical Outcomes Partnership (OMOP) Common Data Model (CDM) and OHDSI related tools, such as ATLAS, ATHENA, and ACHILLES. Proven experience in programming languages commonly used in the OHDSI community, such as SQL, R, and Python. Proven experience in data management, governance, engineering, and strategy. Good understanding of observational study design and epidemiological concepts with an emphasis on RWE data. Familiarity with Machine Learning and Statistical concepts. Understanding of US health payer dynamics would be advantageous. Solid understanding of clinical terminology such as SNOMED, ICD9/10, CPT, HCPCS, and READ. Solid understanding of healthcare data, particularly electronic health records (EHR) and insurance claims, and experience working with healthcare data standards. Strong problem solving skills and the ability to work collaboratively in a team environment. Excellent communication skills, with the ability to convey technical concepts to both technical and non technical stakeholders. Experience developing and maintaining documentation for RWE studies and insight generation. Experience with data quality assessment and data validation techniques for fit for purpose. Benefits You will have access to the most cutting edge technology, the largest data sets, and the best analytics tools, as well as the opportunity to work with 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 therapeutic areas, you can seek opportunities to grow without boundaries. You will play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. It is an exciting time to join and reimagine what is possible in healthcare. 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 and enhance our success. We build an inclusive and respectful culture that nurtures belonging and empowers employees to reach their full potential. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. Learn more at

IQVIA LLC is seeking a Senior Data Scientist in Brighton, UK. This role involves developing and maintaining healthcare data solutions using the OHDSI and DARWIN frameworks. You'll collaborate with cross-functional teams and support RWE projects within the pharmaceutical sector. Qualified candidates should have proven experience with OMOP CDM, proficiency in SQL, R, and Python, and a solid understanding of healthcare data. Join IQVIA to be part of a diverse and inclusive work environment.

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.

IQVIA LLC in Reading is seeking a Clinical Data Management Lead to oversee end-to-end data management delivery for global clinical trials. This fully remote role offers a competitive salary and performance-based incentives. You will lead cross-functional teams, ensuring quality, accuracy, and compliance. Ideal candidates should possess at least 10 years of experience in clinical data management and proficiency with EDC systems like Medidata Rave and Oracle InForm. Join us to help bring new therapies to life!

IQVIA LLC is seeking a Sales Solutions Specialist in Greater London. The role involves developing new business within the pharmaceutical sector through consultative sales, achieving revenue targets, and collaborating with internal teams to enhance client satisfaction. Ideal candidates will possess a Bachelor's degree and a minimum of 3 years' sales or account management experience in the pharmaceutical industry. Competitive compensation and career development opportunities are offered.

Sales Solutions Specialist - Pharma / Life ScienceApplylocations: London, United Kingdomtime type: Full timeposted on: Posted Todayjob 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. Job Overview Develops new business for a specific product specialty, providing the product expertise and sales leadership to identify & qualify revenue opportunities, proactively manage the selling process, and close the sale in both existing and new accounts. Essential Functions • Achieves growth & revenue targets for assigned product through a consultative sales approach that solves client business issues. • Proactively strengthens in-depth knowledge of product and its application within a client's enterprise. • Participates with Account Directors to establish account planning strategy as it relates to assigned product area. • Collaborates with Customer Team to target and validate opportunities for assigned customers / territory. • Interfaces with customer at all levels. • Creates and presents client proposals that result in winning sales. • As necessary, identifies and manages resources to develop proposals that position IQVIA capabilities & solutions to customers. • Monitors delivery, implementation, and customer satisfaction. • Seeks "starburst" opportunities within existing customers to grow revenue opportunities across the IQVIA suite of offerings. • As part of the sales process, gathers market and client intelligence and provides strategic feedback to Marketing, Consulting, Service, and Sales to strengthen offerings and capture additional business. • May have leadership responsibility with less experienced solutions sales personnel. Our Ideal Candidate Will Have • Bachelor's Degree Req • 3 years relevant sales, account management or client-facing support experience Req • Possesses knowledge of key marketplace issues for the pharmaceutical industry and related businesses. • Deep knowledge of one or more IQVIA specialty products along with subject matter expertise relating to client business processes that are improved by the IQVIA solution. Must be a superior and successful sales person, have excellent presentation and writing skills, act with a sense of urgency, and be able to work both independently and within a team environment. • Must have successful experience identifying and closing new business opportunities and developing positive relationships at all levels of client management and within IQVIA sales, consulting and marketing teams. • Must be revenue driven, knowledgeable, consultative, a problem solver, customer focused, creative, resourceful, fast & flexible, team player, organized, and an effective negotiator.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 IQVIATM. 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.

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.

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.

Senior Business Systems Analyst/Product Owner page is loaded Senior Business Systems Analyst/Product Ownerlocations: Livingston, West Lothian, United Kingdom: Reading, Berkshire, United Kingdom: London, United Kingdomtime type: Full timeposted on: Posted Todayjob requisition id: R Senior Business Systems Analyst/Product Owner IQVIA Laboratories IQVIA Laboratories is a global leader in drug discovery and development, offering comprehensive central and specialty biomarker services. Our expertise includes genomics, immunoassays, flow cytometry, anatomic pathology, precision medicine, vaccine assays, ADME, and bioanalytical services. We also specialise in antibody and biomarker discovery and decentralized clinical trial solutions. Committed to scientific rigor and operational excellence, we support all phases of drug development, ensuring high data integrity and accelerating transformative therapies. Join us on our exciting journey! Job Overview: Under general direction, formulate and define systems scope and objectives based on both user needs and a good understanding of applicable business systems and requirements. Analyse business and user needs to facilitate documenting requirements. Own and continuously refine the product backlog Oversee business systems projects from inception through implementation and support - including development, validation testing and user acceptance testing. Query and interpret complex lab data using SQL to inform decisions. Foster cross-functional collaboration to align technology with business goals in clinical trial settings. Guide and advise less-experienced Business Systems Analysts. Competent to work at the highest technical level of most phases of systems analysis while considering the business implications of the application of technology to the current and future business environment. Requirements: Bachelor's Degree in Computer Science or Life Sciences. 10-15 years of experience in IT as a Business Analyst, including 6 years in a Central Lab or Clinical Trials environment preferred. Deep understanding of business applications and client requirements in a regulated setting. Demonstrated experience producing high-quality requirements artifacts (BRDs, functional specs, user stories, acceptance criteria, process flows, data mappings) and partnering across Business/IT. Working knowledge of regulated expectations for computerized systems used in clinical research. Strong SQL skills for querying data in complex systems. Experience with PowerBI. Exceptional communication, documentation, and coordination skills across technical and non-technical teams. Benefits of joining IQVIA Work-Life Balance, with a strong focus on a positive well-being. Continuous career development and growth opportunities. Variety of therapeutic areas Collaborative and supportive team environment Access to cutting-edge and innovative, in-house technology This role is not eligible for UK visa sponsorship. 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 global leader in healthcare innovations is seeking a Senior Business Systems Analyst/Product Owner to enhance product backlogs, oversee projects, and analyze complex lab data using SQL. The role requires a Bachelor's degree in Computer Science or Life Sciences, with 10-15 years in IT and strong communication skills. Benefits include work-life balance, career development, and access to cutting-edge technology. This position is not eligible for UK visa sponsorship.