IQVIA

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. 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 offeringsEngage with pharmaceutical and biotech clients to understand their scientific communication, publication, and content development needsPosition Pharma review's capabilities to prospective and existing clientsWork with scientific and operational teams to develop tailored solutions aligned to client objectivesIdentify opportunities to expand existing client relationships and support new business acquisitionClient Engagement & Solution Development Develop value propositions that demonstrate the impact of high-quality scientific content on client objectivesSupport proposal development, client presentations, and commercial discussionsCollaborate with subject matter experts to create compelling solution narratives and case studiesGather market intelligence and customer feedback to support the evolution of Pharmareview's service offeringsGo-to-Market & Thought Leadership Support the development of sales collateral, client-facing content, and business development materialsPromote awareness of Pharma Review capabilities across IQVIA commercial teamsContribute to thought leadership activities focused on scientific communications, medical writing, publications, and content innovationRepresent Pharma Review at industry conferences and client meetings, as appropriateRequirements  5+ years of experience in business development, account management, medical communications, scientific services, or related commercial roles within life sciencesStrong understanding of scientific communications, medical writing, publications, medical review processes, and content developmentExperience engaging with pharmaceutical and biotech stakeholdersCommercial mindset with a proven ability to identify and develop business opportunitiesAbility to translate client needs into tailored scientific content solutionsExcellent communication, presentation, and stakeholder management skillsExperience working in medical communications agencies, scientific content organizations, CROs, or related service providers is highly desirableDeep knowledge of review and approval  process, and relevant codes (EFPIA, ABPI)Familiarity with AI-enabled content creation, content operations, or digital scientific communications is advantageousWhy 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 https://jobs.iqvia.com IQVIA 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.

Job OverviewProvide medical expertise on pharmacovigilance services to divisions as requested. The Associate Medical Safety Director participates in all aspects of Medical Safety’s involvement on assigned trials and stand alone safety projects with appropriate oversight from management or more senior medical safety directors. Essential Functions• Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality and company summary• Compose, edit and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements• Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported• Provide aggregate reviews of safety information, including clinical data, to maintain oversight of a product’s safety profile• Provide coding review of AEs, Past medical history, Concomitant medications or other medical data listings to verify and medically vet clinical data• Represent safety and clinical data review findings during client meetings• Provide medical review and edits to IND Annual Reports, EU Periodic Benefit Risk Evaluation Reports, EU Periodic Safety Update Reports, EU Development Safety Update Reports, US Periodic Reports• Provide medical review and edits of Development Risk Management Plans, EU Risk Management Plans or US Risk Evaluation and Mitigation Strategies• Provide medical oversight for label development, review and change• Provide medical support and attendance at Data Safety Monitoring Board Meetings• Attends and contributes medical safety evaluation on Safety Monitoring Committees• Provide medical safety contributions to the Integrated Safety Summary or Common Technical Document• Provide medical review and edits to Drug Safety Reports or other benefit-risk assessments• Review and sign off on both the Project Safety Plan and the Medical Monitoring Plan per medical safety scope agreed in contract• Perform Medical Safety review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs) for appropriate safety content and data capture.• Act as Global Safety Physician or Assistant or Back-up on projects as assigned• Attend project meetings, medical safety team meetings, and client meetings as requested• Ensure coverage for all medical safety deliverables within regulatory or contracted timelines• Provide medical escalation support for medical information projects• Provide medical escalation support for EU Qualified Persons for Pharmacovigilance projects• 24 hour medical support as required on assigned projects• Maintain awareness of medical-safety-regulatory industry developments Qualifications• Other A medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education Req• Three (3) years of clinical practice experience (e.g  graduate medical training) with two (2) additional years in the  pharmaceutical or associated industry  in any role. Or equivalent combination of education, training and experience Req• Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research including knowledge of regulations and guidelines pertaining to safety and good clinical practice• Knowledge of clinical trials and pharmaceutical research process• Ability to establish and meet priorities, deadlines, and objectives.• Skills in providing consultation and advice on multiple assignments required, as well as initiative and flexibility• Ability to establish and maintain effective working relationships with coworkers, managers and clients•  A valid medical license, or equivalent, from the country or region in which he/she resides and works  Pref 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 https://jobs.iqvia.com IQVIA 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.

Job OverviewProvide comprehensive Medical Review expertise to provide efficient, quality data management products that meet customer needs. Provide project management support in the areas of structured patient data review per clinician's perspective. Essential Functions• Identify patient anomalies to ensure medical congruency/plausibility of a subject data per protocol.• With minimal guidance, provide project management expertise working with clinical study teams, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections, and provide technical expertise• Maintain strong customer relationships• With guidance, track service performance and provide leadership to identify root causes of issues and implement remedial actions• Ensure timely follow-up and resolution of compliance issues• Serve as Subject Matter Expert (SME)• Continuously look for opportunities to improve efficiency of tasks and quality of deliverables• Provide therapeutic area/indication training for the project clinical team.• Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested. Qualifications• Medic (MBBS) with 2+ years of Experience or MD with any experience/Fresher• Experience in clinical data sciences at a CRO, pharmaceutical company or other medical environment with demonstrated leadership experience Req• Good understanding of clinical/medical data.• Knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology• Must have Medical but also an operational focus towards metrics and status information to take the appropriate actions to resolve.• Excellent communication, interpersonal, customer service, and teamwork skills• Excellent organizational and problem-solving skills• Excellent project management skills and coaching skills• Ability to work with minimal supervision, using available resources,• Ability to work on multiple projects and manage competing priorities• Strong customer focus skills• Ability to establish and maintain effective working relationships with coworkers, managers and clients 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 https://jobs.iqvia.com IQVIA 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.

Job Overview We are seeking an experienced Data / Backend Software Engineer to support data engineering and analytics platforms. The role will focus on building and maintaining scalable data pipelines, enabling efficient data processing, and supporting downstream analytics use cases. The candidate will work in an Agile delivery environment and collaborate closely with engineering and business stakeholders. This position is based in Bangalore/Kochi and follows a hybrid work model. Key Skills Mandatory Skills Strong hands-on experience with PythonExperience working with Apache Spark for large-scale data processingSolid understanding of ETL Development and data pipeline designStrong proficiency in SQL for data analysis and transformationExperience working in an Agile Methodology environmentExposure to CI/CD pipelines for automated build and deploymentQualifications 3+ years of relevant experience in data engineering or backend development rolesBachelor’s degree in Engineering, Computer Science, or a related field (preferred)Strong analytical and problem-solving skillsAbility to work independently and collaborate effectively within cross-functional teamsComfortable working in a hybrid setup from BangaloreIQVIA 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 https://jobs.iqvia.com IQVIA 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 Regulatory Intelligence provides instant access to regulatory insights and real-time updates from national authorities across the globe, helping you to avoid the resource-intensive process of gathering, organizing, and sharing important regulatory information. IQVIA Regulatory Intelligence services cover more than 110 countries, regions, and international organizations. IQVIA RI supports pharmaceutical and medical device companies by providing access to up-to-date and comprehensive original and translated regulatory documents, expert country summaries, tabulated comparative regulatory information covering operational details and timely alerts with state-of-the-art functionality. OVERVIEW OF ROLE – SAFETY PROFILE Based in our India office (Bangalore / Gurgaon), we seek a skilled Individual contributor proficient in applying subject matter expertise. The successful candidate will be responsible for the creation and upkeep of high-quality regulatory intelligence content focusing on Drug Safety & Pharmacovigilance. Knowledge on Device Safety will be an added advantage. Responsibilities also include managing day-to-day operations for IQVIA Regulatory Intelligence, covering planning, client delivery, and maintaining quality standards. RESPONSIBILITIES Prepares, reviews, and updates regulatory documentation in Drug Safety & Pharmacovigilance based on documents published by regulatory authorities as appropriate with particular focus on APAC region, USA, and Canada.Monitoring and analysis of regulatory updates (including laws, guidelines, technical requirements, and trends) issued by relevant regulatory bodies in the territory.Works within cross-functional teams and collaborates with a network of internal/external regulatory experts to ensure the production and maintenance of high-quality (timeliness, completeness, and accuracy) regulatory intelligence related to clinical trials, as per defined quality processes.Performs quality control activities of external expert contributions within the area of clinical trials.Provides knowledge related to safety to support inquiries from customers, sales, marketing, and business development.Acts as a subject matter expert of Regulatory knowledge in Drug Safety as applicable.Understands the scope of work, deliverables, and manages workload as appropriate.May give guidance to colleagues and may assist in their training and development.May conduct and present regulatory training sessions for small groups or individuals within the RI team.REQUIRED KNOWLEDGE, SKILLS, AND ABILITIES Proven experience and tenures working in managing Drug Safety submissions within Life Sciences (within regulatory authority, consultancy, or industry) in the USA, Canada and APAC region.Preferred hands-on experience in drug safety submissions like ICSR and periodic submissions, RMP, Signal, Literature review in the USA, Canada and APAC region.Master’s degree in pharmacy/life sciences.In-depth knowledge of Drug Safety & Pharmacovigilance regulations including:Individual case safety report timeline & submissions to regulatory agencies and ethics committeesPeriodic adverse event report timeline & submissions to regulatory agencies and ethics committeesKnowledge about Risk Management Plans, Signal Detection & Literature ReviewAbility to assess impact of new regulatory requirements.Ability to understand and interpret regulatory developments (guidelines, regulations, and laws) to understand, anticipate, interpret, and communicate regulatory trends and requirements.At least 3-4 years relevant experience.Ability to communicate clearly and effectively (verbally and written) and experience in writing summaries/reports for different audiences.Strong attention to detail, proactive and highly organized.Knowledge of quality management within Life Sciences.Ability to establish and maintain effective working relationships with co-workers, managers, and clients.Strong software and computer skills, including Microsoft Office, publishing applications and tools, as applicable.Leverage approved AI tools (e.g., Copilot or equivalent platforms) to support regulatory intelligence activities such as document summarization, trend identification, AI Prompting and draft content generation will be an added advantage.Demonstrates self-motivation and enthusiasm.Ability to work on several projects, with direction from senior staff as appropriate.Ability to follow standard operating procedures consistently; provides independent thought to assist in process improvements.Ability to adapt quickly to a rapidly changing environment. 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 https://jobs.iqvia.com IQVIA 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 advanced analytics, technology solutions and clinical research services to the life sciences industry, dedicated to creating intelligent connections that deliver unique innovations and actionable insights. We help to speed drug development, ensure product quality and safety, improve commercial effectiveness, get the right treatments to patients, improve access and delivery of healthcare, and ultimately drive better health outcomes. With approximately 90,000 employees, IQVIA conducts operations in more than 100 countries. We are currently looking for a Global Head of Offering Development – Lifecycle Management to join IQVIA. Commercial Brand Outsourcing or Lifecycle management represents a significant share of sales across launch and established brand portfolios of pharmaceutical companies that can be deprioritized, with potential revenue and profit growth remaining untapped. In this role, you will define and evolve market-leading offerings in partnership with key stakeholders, ensuring strong competitive differentiation and alignment with client needs. You will collaborate closely across business units to translate technical capabilities into compelling client solutions, support business development activities, and provide best-practice guidance throughout the sales cycle. Acting as a central connector across IQVIA’s expertise, you will help shape best-in-class solutions and contribute to successfully closing strategic business opportunities. Essential Functions Partner with key IQVIA stakeholders and external partners to develop competitive, differentiated lifecycle management offerings, addressing prioritized market opportunities and portfolio gaps. Conduct marketplace and competitive analysis to identify trends and quantify high-value growth opportunities, particularly across established and mature brands. Collaborate across IQVIA service lines to design and promote integrated, multi-capability solutions, strengthening strategic and commercial linkages across the organization. Maintain an advanced understanding of IQVIA’s service offerings and provide subject matter expertise and best practice guidance throughout the sales cycle. Support business development activities by contributing to RFPs, RFIs, and proposal defense meetings, helping translate capabilities into compelling client value propositions. Develop target market insights, strategic analyses, and client-ready materials to support engagement and commercial success. Contribute to the development of marketing materials and campaigns that effectively position and differentiate offerings in the marketplace. Provide strategic input into business unit planning, including identification of growth opportunities and market priorities. Build and maintain strong relationships with internal stakeholders across a global, matrixed organization, enabling effective solution development and delivery. Lead and manage team members in line with organizational policies, including work allocation, performance management, coaching, and professional development, while addressing employee relations as needed. Key Responsibilities Lead the Commercial Brands Outsourcing (CO) Strategy and Offering Initiative across IQVIA Global Commercial Solutions, ensuring alignment with our go to market colleagues, regional strategies and business priorities to shape the overall direction and deliver against plan Coordinate with regional teams to identify, assess, and activate opportunities for established brands, leveraging local insights and capabilities Act as a commercial expert, defining and sharing best practices for commercial terms while managing enterprise risk Serve as a solution and subject matter expert for clients, supporting business development teams throughout RFIs, RFPs, and client engagements Develop and continuously evolve the global CO offering, ensuring alignment with client needs and IQVIA’s broader commercial strategy Identify and enable channel and capability partnerships to enhance solution delivery and scalability Manage key internal and external stakeholders, fostering alignment, engagement, and accountability across functions and geographies Qualifications & Experience Bachelor’s degree required; MBA or advanced business/scientific qualification preferred, or equivalent combination of education and experience. 12–15+ years of relevant experience within the pharmaceutical, biopharmaceutical, consulting, or agency environment, including at least 4 years of senior leadership experience. Strong knowledge of the biopharmaceutical industry, including commercial models, portfolio strategy, and lifecycle management. Demonstrated experience in offering development, commercial strategy, or portfolio/brand strategy, ideally including established or mature brands. Proven track record of working in global, matrixed, multi-regional organizations, delivering complex cross-functional initiatives. Exceptional leadership, communication, presentation, and stakeholder influencing skills. Strong ability to influence senior stakeholders both internally and externally Strategic mindset with the ability to translate market trends into actionable business opportunities. Proven ability to operate in a fast-paced, dynamic environment, managing multiple priorities and changing timelines. Strong analytical, problem-solving, and decision-making capabilities, with the ability to develop clear recommendations. Excellent organizational, planning, and project management skills High level of resilience and stress tolerance, with a collaborative and team-oriented approach. Experience in people management, including coaching, development, and handling complex employee scenarios. Strong attention to detail while maintaining a big-picture strategic perspective. Proficiency in MS Office and standard business tools. 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 https://jobs.iqvia.com IQVIA 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 the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Within our Sponsor dedicated model, our team contributes to the pipelines of the specific sponsor and therefore our CRAs are ‘indication and molecule experts’. We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study. Leadership recognises the skills, talent and experience of our clinical teams and strives to build upon this as the function evolves and grows. Our managers understand the sponsors priorities and the individual aspects of each model. Focus is given to career development from day one, including new hire orientation and onboarding, day to day problem solving and training and development. Additionally, IQVIA’s sponsor dedicated business works with the Sponsors SOP’s, creating more continuity for both parties. Our models offer excellent opportunities for experienced CRA’s to expand their knowledge and skills. IQVIA Netherlands are currently seeking motivated Clinical Research Associate II practitioner to join our unique and dynamic Sponsor dedicated model. This is a role based in the Netherlands Your Role: Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesWork with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.Collaborate and liaise with study team members for project execution support as appropriate.If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.Your Profile: Bachelor's Degree Degree in scientific discipline or health careMinimum of 12 months of independent, on-site monitoring experience as a CRA within a CRO or pharmaceutical environment.Full professional fluency in both Dutch (minimum C1 level) and English, including strong medical writing skills for reports.Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).Organizational and problem-solving skills.Exceptional interpersonal and cross-cultural communication skills to build strong, trusted partnerships with Dutch site investigators and medical staff.A collaborative mindset to work effectively with cross-functional global teams, project managers, and local study coordinators.What we offer: Choice of a company car (eligible for private use) or a flexible mobility allowance, fully covering fuel, insurance, and maintenance.Premium technology bundle to support your daily operations, including a laptop and an iPhone.Strong focus on career advancement, featuring dedicated training programs, learning resources, and pathways to build clinical or leadership expertise. Home office setup support, alongside an annual wellness reimbursement to fund your sports and wellbeing activities.Comprehensive time-off policy, including competitive annual vacation days and flexible year-end leave options.Premium benefits package featuring a robust pension plan, multiple corporate insurance coverages, and social activities.Optional partial reimbursement for supplementary health insurance policies to support your healthcare needs.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 https://jobs.iqvia.com IQVIA 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 the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Within our Sponsor dedicated model, our team contributes to the pipelines of the specific sponsor and therefore our CRAs are ‘indication and molecule experts’. We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study. Leadership recognises the skills, talent and experience of our clinical teams and strives to build upon this as the function evolves and grows. Our managers understand the sponsors priorities and the individual aspects of each model. Focus is given to career development from day one, including new hire orientation and onboarding, day to day problem solving and training and development. Additionally, IQVIA’s sponsor dedicated business works with the Sponsors SOP’s, creating more continuity for both parties. Our models offer excellent opportunities for experienced CRA’s to expand their knowledge and skills. IQVIA Netherlands are currently seeking motivated Senior Clinical Research Associate practitioner to join our unique and dynamic Sponsor dedicated model. This is a role based in the Netherlands Your Role: Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. Collaborate and liaise with study team members for project execution support as appropriate. If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Your Profile: Bachelor's Degree Degree in scientific discipline or health care Minimum of 3 years of independent, on-site monitoring experience as a CRA within a CRO or pharmaceutical environment. Full professional fluency in both Dutch (minimum C1 level) and English, including strong medical writing skills for reports. Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Organizational and problem-solving skills. Exceptional interpersonal and cross-cultural communication skills to build strong, trusted partnerships with Dutch site investigators and medical staff. A collaborative mindset to work effectively with cross-functional global teams, project managers, and local study coordinators. What we offer: Choice of a company car (eligible for private use) or a flexible mobility allowance, fully covering fuel, insurance, and maintenance. Premium technology bundle to support your daily operations, including a laptop and an iPhone. Strong focus on career advancement, featuring dedicated training programs, learning resources, and pathways to build clinical or leadership expertise. Home office setup support, alongside an annual wellness reimbursement to fund your sports and wellbeing activities. Comprehensive time-off policy, including competitive annual vacation days and flexible year-end leave options. Premium benefits package featuring a robust pension plan, multiple corporate insurance coverages, and social activities. Optional partial reimbursement for supplementary health insurance policies to support your healthcare needs. 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 https://jobs.iqvia.com IQVIA 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 the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Within our Sponsor dedicated model, our team contributes to the pipelines of the specific sponsor and therefore our CRAs are ‘indication and molecule experts’. We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study. Leadership recognises the skills, talent and experience of our clinical teams and strives to build upon this as the function evolves and grows. Our managers understand the sponsors priorities and the individual aspects of each model. Focus is given to career development from day one, including new hire orientation and onboarding, day to day problem solving and training and development. Additionally, IQVIA’s sponsor dedicated business works with the Sponsors SOP’s, creating more continuity for both parties. Our models offer excellent opportunities for experienced CRA’s to expand their knowledge and skills. IQVIA Netherlands are currently seeking motivated Clinical Research Associate I practitioner to join our unique and dynamic Sponsor dedicated model. This is a role based in the Netherlands Your Role: Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. Collaborate and liaise with study team members for project execution support as appropriate. If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Your Profile: Bachelor's Degree Degree in scientific discipline or health care Minimum of 3 months of independent, on-site monitoring experience within a CRO or pharmaceutical environment. Full professional fluency in both Dutch (minimum C1 level) and English, including strong medical writing skills for reports. Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Organizational and problem-solving skills. Exceptional interpersonal and cross-cultural communication skills to build strong, trusted partnerships with Dutch site investigators and medical staff. A collaborative mindset to work effectively with cross-functional global teams, project managers, and local study coordinators. What we offer: Choice of a company car (eligible for private use) or a flexible mobility allowance, fully covering fuel, insurance, and maintenance. Premium technology bundle to support your daily operations, including a laptop and an iPhone. Strong focus on career advancement, featuring dedicated training programs, learning resources, and pathways to build clinical or leadership expertise. Home office setup support, alongside an annual wellness reimbursement to fund your sports and wellbeing activities. Comprehensive time-off policy, including competitive annual vacation days and flexible year-end leave options. Premium benefits package featuring a robust pension plan, multiple corporate insurance coverages, and social activities. Optional partial reimbursement for supplementary health insurance policies to support your healthcare needs. 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 https://jobs.iqvia.com IQVIA 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.

Job OverviewUnder guidance, bridges and codes data into IQVIA systems. Essential Functions• Codes data, as required, transforming incoming paper data from suppliers to electronic data files.• Interprets written responses and enter into electronic coding systems allocating data to standard reference systems.• Performs quality assurance on coded data to ensure it accurately reflects the paper data submission.• Bridges data, comparing incoming transaction data with IQVIA’ reference data files to make a match or bridge between the two using manual or automated processes. Qualifications• High School Diploma or equivalent  Req• Three (3) years work experience in which PC literacy skills including Word, Excel have been gained. Req• Ability to carry out some analysis and information gathering to resolve problems on routine matters.• Developing knowledge of the company's products and pharmaceutical industry. 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 https://jobs.iqvia.com IQVIA 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™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheitsversorgung zu erzielen. Werden Sie Teil unserer Community von rund 86.000 Mitarbeiterinnen und Mitarbeitern in über 100 Ländern, die sich dafür einsetzen, das Potenzial von Human Data Science Wirklichkeit werden zu lassen! Ganz gleich, in welche Rolle Sie bei IQVIA einsteigen, es erwartet Sie ein offenes, innovationsfreudiges Umfeld, in dem Sie sich viel bewegen können. Finden Sie heraus, wie Sie Ihre Talente und Ihre Leidenschaften bei IQVIA einbringen können. Im Bereich Commercial Engagement Services (CES) arbeiten wir eng mit unseren Life Sciences-Kunden zusammen und unterstützen sie mit flexiblen Vertriebs- und Personallösungen für nachhaltigen Erfolg am Markt. Dies umfasst insbesondere die Rekrutierung, das Training und die Steuerung des Vertriebsteams in Dienstleistungsprojekten bzw. in Arbeitnehmerüberlassung. Dabei differenzieren wir uns über integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Komm in unser IQVIA-Team! Für ein spannendes Projekt im Bereich Adipositas suchen wir Pharmaberater (m/w/d) zum nächstmöglichen Zeitpunkt Im Gebiet: Dinslaken, Wesel, Geldern, Goch, Kleve, Kevelaer   Das sind Deine Aufgaben: Durchführung von Verkaufsgesprächen mit Fachgruppen in Praxen, Kliniken und Apotheken (Diabetologen, Internisten, Hausärzten, Kardiologen, Nephrologen, Apotheker), unter Nutzung digitaler Kommunikationskanäle Umsetzung der Verkaufs- und Marketingstrategien Entwicklung und Umsetzung von Gebietsaktionsplänen und Kontaktstreckenplanung Organisation und Durchführung von Fortbildungsveranstaltungen, auch digital Mitgestaltung bei Veranstaltungen und Workshops Das bringst Du mit: Du hast ein naturwissenschaftliches Hochschulstudium absolviert oder eine Ausbildung zum geprüften Pharmareferenten (m/w/d) gemäß §75 AMG abgeschlossen Du bringst Berufserfahrung in einer vergleichbaren Position mit Verkaufskompetenz: Ausgeprägte verkäuferische Fähigkeiten und Ambitionen, nachweisbare Erfolge im Außendienst. Digitale Affinität: Sicherer Umgang mit digitalen Kommunikationskanälen sowie Bereitschaft, neue digitale Funktionen und Arbeitsweisen schnell zu adaptieren Soft Skills: Hohe soziale Kompetenz, Teamfähigkeit, Netzwerkkompetenz sowie eigenverantwortliches und integres Handeln. Pioniergeist: Bereitschaft, ein junges Indikationsgebiet aktiv mit aufzubauen und Top-Kunden für innovative Therapien zu entwickeln. Patientenorientierung: Mit Leidenschaft für die Verbesserung der Versorgung von Menschen mit Adipositas im Einsatz – auch außerhalb der eigenen Komfortzone Sprachkenntnisse: Gute mündliche und schriftliche Englischkenntnisse. Mobilität: Führerschein Klasse B und Reisebereitschaft im Gebiet. Das erwartet Dich bei uns: Ein attraktives Gehaltspaket plus Kundenprämien, vielfältige Corporate Benefits, betriebliche Altersvorsorge sowie 24/7 Unfallversicherung (auch für den privaten Bereich) und exklusive private Krankenzusatzversicherungen Ein top ausgestatteter Firmenwagen verschiedener Premiumanbieter mit uneingeschränkter Privatnutzung (ohne Zuzahlung) und mit Wahlmöglichkeit des Modells Eine moderne IT-Ausstattung für Deinen modernen digitalen Arbeitsplatz Unser unbefristetes IQVIA Arbeitsverhältnis bietet Sicherheit und eine langfristige Perspektive Wir bieten u.a. tarifliche Sonderurlaubstage, Umzugszuschuss bei betrieblich bedingtem Wechsel deines Wohnorts Eine hohe Übernahmequote durch unsere Kunden ermöglicht Dir den Karrierestart bei zukunftsweisenden und führenden Unternehmen der Pharmabranche und Medizintechnik-Branche Vielfältige und individuelle Weiterentwicklungsmöglichkeiten auch innerhalb von IQVIA (z.B. Führung, Key Account Management, Projektmanagement und vieles mehr) Wir begleiten Dich während Deiner Bewerbungsphase durch individuelle Betreuung/Vorbereitung bis zur Einstellung und auch darüber hinaus während des Beschäftigungsverhältnisses Unser Kunden-Netzwerk reicht vom Start-up Unternehmen bis zum Global Player. Gemeinsam mit Dir finden wir den richtigen Job für Dich! Starte Deine Karriere mit IQVIA! Dein besonders schneller Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: [email protected] #LI-CES #LI-DNP #LI-SS2 #Pharmaberater #Biologie #Chemie #Pharmareferent #BTA #CTA #PTA #Pharmazie #Pharma-Außendienst #Diabetes #Facharzt #Klinik #Adipositas #Gynäkologie #Kardiologie #Nephrologie 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 https://jobs.iqvia.com IQVIA 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.

Job Overview This Associate Director will sit within the Data Management organization and at the center of how IQVIA Digital scales data-driven products securely, compliantly, and efficiently. The Governance and Data Management Operations Enablement lead is responsible for operationalizing data governance and compliance requirements, along with setting clear operating models, repeatable processes, and practical enablement across Data Management and the enterprise. As a highly visible, cross-functional leader, this role partners closely with Data Management, Product, and Information Governance to ensure data use, documentation, and compliance practices are consistently executed without slowing innovation. The role also serves as the primary representative for IQVIA Digital in enterprise data governance forums, helping shape standards that support both regulatory rigor and product velocity. Key Responsibilities Governance Leadership & Representation Serve as the primary IQVIA Digital representative on enterprise data governance committees and boardsLead data governance and compliance initiatives in close partnership with IQVIA Information Governance  Ensure consistent application of data governance, compliance, and documentation standards across IQVIA Digital data management and productsOperating Model & Enablement Develop, implement, and document cross-organization operating models, including Standard Operating Procedures (SOPs), Business Requirement Documents (BRDs), workflow diagrams (e.g., Lucidchart), and governance frameworksCreate, standardize, and operationalize Data Use Agreements (DUAs), Data Dictionaries, Data Catalogs, and related governance artifactsDrive operational efficiency through standardization, clear documentation, and scalable enablement practicesExecutive Communication & Knowledge Management Own and evolve the Data Management SharePoint site as the authoritative source for design, processes, and documentationDevelop high-quality, executive-ready materials for senior leadership, governance committees, and external stakeholdersTranslate complex technical and regulatory concepts into clear, actionable guidance for cross-functional teamsQualifications 10+ years of experience spanning data management, data governance, compliance, data-driven operations, website design, program management, or related disciplinesExperience operating in regulated environments such as health, pharmaceutical, life sciences, and/or ad-techStrong working knowledge of data governance frameworks, regulatory requirements, and enterprise compliance practicesProven ability to partner effectively with Data Management, Product, GTM, Leadership, and Information Governance teamsExceptional ability to operate in highly matrixed, cross-functional environments and influence without direct authorityDemonstrated strength in executive communication, processes, documentation, and stakeholder managementExceptional organization and execution skills, including effective prioritization, critical thinking, stakeholder management (up and down), and strong accountability ownershipBachelor’s degree required; advanced degree preferredIQVIA 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 https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA 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. The potential base pay range for this role, when annualized, is $84,400.00 - $235,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.• Collaborate and liaise with study team members for project execution support as appropriate.• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications• Bachelor's Degree Degree in scientific discipline or health care preferred. Req• Requires at least 1 year of on-site monitoring experience. Req• Equivalent combination of education, training and experience may be accepted in lieu of degree. Req• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).• Good therapeutic and protocol knowledge as provided in company training.• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).• Written and verbal communication skills including good command of English language.• Organizational and problem-solving skills.• Effective time and financial management skills.• Ability to establish and maintain effective working relationships with coworkers, managers, and clients. 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 https://jobs.iqvia.com IQVIA 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.

• Job Description Summary Job Overview Provides high quality, on-time input to client projects in the life sciences field. Assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex solutions. May serve as project leader for small teams or work streams.Essential Functions Project manager and point of contact for driving the largest PSP program in collaboration with regulatory and pharma clientsAssists with the review and analysis of client requirements or problems and assists in the development of program design and client solutionsPerforms quantitative or qualitative analyses to assist in the identification of client issues and the development of client specific solutions Assists in the development of detailed documentation and specifications by guiding the teamPerforms quantitative or qualitative analyses to assist in the identification of client issues and the development of client specific solutionsPerforms quality assurance and control measures for a national program across the regionAssists in the design/structure and completion of presentations that are appropriate to the characteristics or needs of the audienceDevelop and oversee the training and onboarding activities related to Patient Services across the regionDevelop thought leadership and case studies related to Patient ServicesProactively develops a basic knowledge of consulting methodologies and the life sciences market through the delivery of Patient Support engagements and participation in formal and informal learning opportunitiesEngagement-based responsibilities are assigned and managed by Engagement Managers or PrincipalsQualifications Bachelor’s or Master’s degree in pharmacy, medical or life sciences (Saudi National)Minimum of 8–10 years of related experience in patient support, market access, and the pharma industry (hospital experience is an added advantage)Works effectively with others across the organization to accomplish team goalsKnowledge of fundamental business processes, their interaction, and the impact of external/internal influences on decision makingKnowledge of consulting methods, tools, and techniques related to the functional areaKnowledge of current industry developments and major competitorsUnderstanding of the marketplaceAwareness of professional/trade associations, key people, and companiesEffective time management skillsIQVIA 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 https://jobs.iqvia.com IQVIA 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 The Human Data Science Company™, focused on leveraging 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 advancements in information, technology, analytics, and human ingenuity to drive healthcare forward. We are currently seeking professionals interested in being part of a major project with an important business partner. We are looking for a Medical Science Liaison (MSL) with experience in Internal Medicine, who will be responsible for strengthening scientific relationships with Key Opinion Leaders (KOLs) and healthcare professionals, as well as providing strategic medical support within their therapeutic area. This position operates primarily remotely, with participation in in-person activities as business needs require. 🩺 ResponsibilitiesEstablish and maintain scientific relationships with KOLs and healthcare professionalsCommunicate medical and scientific information clearly, ethically, and based on evidenceIdentify relevant clinical insights for the businessProvide medical support to internal teams (commercial, market access, marketing, etc.)Participate in congresses, medical events, and scientific activitiesEnsure compliance with regulatory and compliance standards🎓 RequirementsMedical degree (MD)Previous experience as an MSL (required)Experience in Internal Medicine (preferred)Strong knowledge of the pharmaceutical industryHybrid work model: although most activities are virtual, in-office attendance is required depending on the business unit (Viaducto, Río Becerra); availability to travel and attend events as neededExcellent communication, analytical, and relationship-building skills#LI-CES 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 https://jobs.iqvia.com IQVIA 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 Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. IQVIA Biotech is seeking an experienced Clinical Project Manager based in Mexico to lead and deliver innovative clinical trials in Cardiovascular, Renal and/or Metabolic As a Project Lead, you’ll drive operational excellence, manage cross-functional teams, and ensure high-quality delivery that accelerates life-changing therapies to market. Key Responsibilities: Lead global/regional clinical trials from start-up through close-out.Develop and execute study management plans aligned with contract and strategy.Manage timelines, budgets, and risk mitigation across projects.Serve as the primary contact for sponsors and vendors.Ensure compliance with ICH-GCP and regulatory standards.Mentor and support project team members.Qualifications: Bachelor’s degree in Life Sciences or related field.Minimum 5 years of clinical research experience, including 1+ year in project management.Strong therapeutic expertise in Cardiovascular preferred.Proven leadership, communication, and problem-solving skills.Solid understanding of project financials and contract management.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 https://jobs.iqvia.com IQVIA 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.

Job OverviewEntry of clinical data into Clinical Data Management Systems and administration of documents to produce efficient, quality data management products that meet customer needs. Education : Pharma or Life science graduates only Location : Kochi, Hybrid Will be considering Recent graduates/Freshers only. Essential Functions• Perform the role of Data Entry Associate, File room Associate, Scanning Associate, Indexing Associate, or other role as defined by manager. Process, log, and track clinical study documents in accordance with CRF Tracking and Data Entry Guidelines. Process and enter data accurately and in a timely manner in accordance with CRF Tracking and Data Entry Guidelines. Understand and comply with core operating procedures and working instructions. Assist in the maintenance of Data Management Study files. Meet objectives as assigned. Develop and maintain good communications and working relationships within CDM team. Qualifications• Equivalent combination of education, training and experience in lieu of degree.• Good organizational and communication skills. Excellent computer skills. Ability to exercise excellent attention to detail. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Good organizational and communication skills. Excellent computer skills. Ability to exercise excellent attention to detail. Ability to establish and maintain effective working relationships with coworkers, managers and clients. 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 https://jobs.iqvia.com IQVIA 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 Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. IQVIA Biotech is seeking an experienced Clinical Project Manager based in Argentina to lead and deliver innovative clinical trials in Cardiovascular, Renal and/or Cardiovascular. As a Project Lead, you’ll drive operational excellence, manage cross-functional teams, and ensure high-quality delivery that accelerates life-changing therapies to market. Key Responsibilities: Lead global/regional clinical trials from start-up through close-out. Develop and execute study management plans aligned with contract and strategy. Manage timelines, budgets, and risk mitigation across projects. Serve as the primary contact for sponsors and vendors. Ensure compliance with ICH-GCP and regulatory standards. Mentor and support project team members. Qualifications: Bachelor’s degree in Life Sciences or related field. Minimum 5 years of clinical research experience, including 1+ year in project management. Strong therapeutic expertise in Cardiovascular preferred. Proven leadership, communication, and problem-solving skills. Solid understanding of project financials and contract management. 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 https://jobs.iqvia.com IQVIA 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.

职位概要  积极为现有客户和新客户的决策者等提供专业化的咨询和开展商务拓展活动以获取和保留业务。建立并 维护与客户间的长期合作关系。负责从洽谈客户开始直至合同结束期间全部的商务工作，包括协助对 RFI/RFP的反馈及商务提案等。   职责  • 积极在现有和特定的潜在新客户间充分挖掘新的商业机会。  • 在业界充分积累人脉并善于辨别商机。 • 与销售管理团队合作以辨别目标客户的商机并进行季度或半年度的列表分析。  • 计划并实施对每个目标客户的整套销售流程，确保对客户的销售策略和方法的正确性。监督销售方案 的实施和达成结果。  • 负责从发掘潜在客户或维系原有客户开始至合同结束期间全部的商务工作。  • 为各业务部门的竞标会议、合同洽谈和拟定、提案等过程提供全程商务支持。  • 向直线经理汇报与商务拓展活动相关的所有数据、过程及结果，并依照直线经理的要求提交商务拓展 的业务报告。  • 主导整个商务进程；准备并负责相关市场或竞标过程中商务相关的PPT演示。  • 协作并拟定合同方案，处理合同后续所有商务相关问题，以确保合同的正常执行。  • 负责建立和制定公司的商务拓展的流程及政策，通过不断调整和优化SOP，确保商务拓展相关工作 的高效运行。  • 针对客户的需求提供高标准、有创新性的建议；跟进客户对提议的反馈；维护客户和合同的数据及进 展的更新。监督合同执行情况并确保其正常执行。  • 及时应对客户咨询和要求。  • 通过参加各种行业展会并在行业研讨会上发言以支持公司市场销售活动  • 在直线经理的指导下，持续关注行业动态，确保各信息渠道的通畅性。  • 确定和提供商务战略信息，以支持业务发展的年度计划。  • 在所需的报告系统（如CRM）中维护记录，并及时准确的更新。  • 支持并改进价格运算以确保和促进合同提案预算的规范性。  • 根据工作需要，可能需要经常出差。  • 完成直线经理分配的其他工作。     所需知识、技能和能力  ·充分理解药物研发和研究的原则。   ·充分了解企业和行业的发展趋势，并具备诠释相关的业务发展趋势的能力。  ·优秀的分析和研究能力，能够评估和解释客户的业务数据。 · 优秀的计算机技能，包括熟练应用办公系统软件如微软Word、Excel和PowerPoint等。   · 优秀的口头和书面英语沟通能力。 · 良好的组织和解决问题的能力。    · 对细节关注度高。 · 有效的时间管理技巧，能够同时处理多个工作的能力。    · 良好的团队协作能力。   学历和经验要求  ·商务或生命科学相关专业优先，大学本科及以上学历。  ·拥有4年及以上临床研究、销售、业务拓展或销售支持工作经验，有CRO公司从业经历优先。 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 https://jobs.iqvia.com IQVIA 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.

职位概要  独立处理注册事务相关的各种工作，担任独立项目的负责人。为低年资注册事务员工提供培训和 指导。   职责  • 为项目分析评估及注册策略的制订提供法规方面的专业支持。  • 对于新项目，需要制订注册方面的预算以及提案，并通过直线经理的审核。  • 为业务拓展部门提供支持，根据直线经理安排，可能参加技术服务竞标会，以及通过电话或当 面与客户进行注册策略方面的交流。  • 对项目相关的工作范围、交付成果、预算、时间表和工作量以及工作范围之外的其他工作进行 详细评估和管理。确保营收被认可，并根据需要向合适的高级职员寻求指导。  • 独立担任注册项目负责人。按照公司相关SOP制订项目计划和预算，管理项目流程和财务状况。 负责申报资料的审核及整理撰写、样品注册检验，负责内部及外部沟通，接受直线经理的审核。  • 与客户及药监部门建立并维护良好的工作关系。  • 根据安排，可能需要负责注册SOPs的撰写或审核。  • 学习并执行公司相关SOPs，并对SOPs提出合理的修改建议和意见，完善相关流程。  • 可能需为低资历同事提供注册法规及注册技术要求方面的培训和指导，并在他们的培训与发展 中提供帮助。 • 根据直线经理安排，可能需要准备注册法规方面的培训资料并为其它职能部门的员工提供培训。  • 参加公司、注册官方机构等提供的注册相关培训；学习注册法规相关文件，提高专业能力以满 足工作要求。 • 根据工作需求，完成注册法规方面的咨询。  • 根据工作需要，可能需要不定时出差。  • 完成直线经理安排的其它工作。      所需知识、技能和能力  • 深入了解中国注册相关政策法规。    • 良好的人际交往能力（口头及书面）和谈判技巧。    • 发现问题和独立解决问题的能力。  • 较好的英语听说读写能力。  • 良好地计算机技能，熟练使用微软Word、Excel及PowerPoint，熟练使用笔记本电脑。  • 有效的时间管理能力，能在最低程度的督导下有效管理多重任务时的优先次序。 • 在保证质量和时间的情况下，能同时工作于多个项目。  • 能够与同事、领导及客户建立并维护有效的工作关系。  • 仅需高级职员最低程度的审核即可处理注册事务的各项工作。    学历和经验要求  • 生命科学相关专业或同等专业本科及以上学历。     • 2年及以上注册事务方面的工作经验。   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 https://jobs.iqvia.com IQVIA 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.

职位概要  按照要求提供生物统计学和统计编程方面的专业知识。参与所分配项目中与生物统计相关的服 务，包括提供一般的生物统计方面的建议，完成方案中统计方法部分，审阅数据库和病例报告表 等。准备统计分析计划，为统计学表、图、列表撰写说明。与客户就研究方案或客户提出的统计 分析问题进行讨论。编写或审核统计分析程序，并审核统计分析结果。就研究时间表、数据质量 和结果的解释与研究团队成员进行沟通。解释分析结果、撰写和审核统计分析报告，或撰写研究 报告中的统计部分等。    职责  • 负责组织和管理所分配项目的统计分析工作。  • 严格按照SOP，在规定的时间内完成项目工作。  • 为临床试验方案设计提供统计学支持。  • 根据项目需要撰写样本量计算报告。  • 撰写或审核SAP，如SAP中统计分析方法的具体规定和统计学图表的设计等。  • 撰写随机化说明文档，并编写随机化程序，生成随机化资料,或者承担审核者。  • 参与DM会议，对CRF、数据库设计进行统计学审核。  • 审核统计分析程序和统计分析数据集，并审核统计分析结果。  • 负责撰写统计分析报告或研究报告中的统计部分。  • 参与开发统计分析函数库及其他应用程序。  • 为经验较少的员工提供统计方面的指导和培训。  • 根据工作需要，可能需要不定时出差。  • 完成直线经理分配的其他工作。      所需知识、技能和能力  • 丰富的临床研究相关知识。  • 熟悉生物统计相关的指南。  • 有扎实的生物统计理论知识及应用经验。  • 熟悉临床试验使用的常用的及较为复杂的统计分析方法。  • 深入了解SAS计算机软件包及良好的编程技能/技术写作技能  • 有效的同时承担多项任务和项目的能力。  • 良好的口头和书面沟通能力（包括能熟练应用英语）。  • 能够项目团队人员进行良好的项目沟通，保持高效的工作效率。  • 能始终遵循SOP要求。  • 重视并履行服务质量方面的承诺，能够在规定的时间节点内完成生物统计分析工作。   学历和经验要求  • 统计学及其相关专业博士及以上学历，有1年及以上的生物统计相关工作经验；或统计学及其 相关专业硕士及以上学历，有3年及以上的生物统计相关工作经验；或统计学及其相关专业本 科及以上学历，有5年及以上生物统计相关工作经验。 上述有关此职位描述的信息是根据此职位的总体性质和岗位级别制定的。不包括或不能理解为是 有关此职位的所有任务、职责和要求的全部说明。 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 https://jobs.iqvia.com IQVIA 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.

职位概要  • 负责公司培训系统的建立、维护、管理、更新和执行。 • 负责建立、组织和执行质量控制计划。对临床部门执行的项目实施质量控制检查，确保临床 研究项目根据试验方案、标准操作规程（SOP）、药物临床试验质量管理规范（GCP）、适用 的法律法规及合同的约定进行。  • 负责协调公司的程序文件（标准操作规程（SOP）、公司政策、工作指南等）的管理。    职责  • 根据公司政策和SOP的要求，建立和维护公司培训系统及流程。培训系统主要为临床监查员团 队和临床研究协调员团队对提供培训。制定公司的培训流程并保证其得到相应执行。    • 定期和相关岗位的直线经理沟通讨论，确定和更新各岗位的培训计划。    • 根据培训计划建立相关的培训资料，并及时跟进行业进展以及法律法规的发展，结合公司业 务发展需求和岗位设置等，定期回顾和更新相关培训材料。确保培训质量。    • 向公司所有员工提供ICH-GCP，中国GCP和相关法律法规的培训。    • 向公司员工提供临床研究的基础及日常培训。    • 向临床监查员团队和临床研究协调员团队提供相应的工作技能培训。    • 和人力资源以及各业务部门负责人及时沟通，协调安排公司的整体培训策略和计划，确保新 员工在加入公司后能够地得到及时培训，从而保证工作质量。确保公司培训资源最高效化。    • 协调安排公司其他类型的培训，例如医学知识培训等。    • 协助其直线经理维护公司的培训系统，确保相关需求和问题得到及时解决。    • 和各临床部门的负责人一起建立各临床业务部门的内部质量控制计划（包括临床监查、项目 管理和研究中心管理部门），经与其直线经理沟通协调后，最终得到首席运营官的批准。    • 和各临床部门的负责人一起，按照质量控制计划的要求，完成所需的质量控制工作。并将相 应的结果和建议与其直线经理沟通协调后，及时反馈给员工和直线经理。  • 参与制定或审阅项目特定质量控制计划及风险管理计划。  • 将在质量控制工作中发现的问题和相应的建议组织成相应的培训课程。    • 推动或主持制定持续改进工作程序和服务质量的措施。  • 如需要，监督员工档案的维护，确保员工档案的管理符合公司标准操作规程的要求。  • 提供GCP领域质量相关问题的咨询。  • 负责维护和更新本部门的SOPs及相关制度等。    • 监督协调SOP的管理（生成，更新，审阅，批准，归档的流程），确保其符合公司标准操作规 程要求。    • 负责协调公司的程序文件（公司政策,工作指南等）的管理，确保所有程序文件及时更新，得 到适当的维护。  • 负责与其他职能部门共同合作。 • 根据工作需要，可能需要经常出差。  • 完成直线经理分配的其他工作。      所需知识、技能和能力  • 丰富的临床研究相关知识以及法律法规知识, 熟悉临床监查及项目管理的过程。    • 熟练的计算机技能，包括应用微软Word、Excel和PowerPoint。  • 优秀的表达能力和书面沟通能力（包括能熟练应用英语）。  • 良好的培训能力和技巧, 优秀的计划、组织和解决问题的能力。    • 有效的时间管理技巧和处理工作冲突的能力。  • 善于团队合作，有与同事、经理和客户建立和维护高效工作关系的能力。    • 能始终遵循SOP要求。  • 能独立工作，独立思考，改进流程。      学历和经验要求 • 临床医学、药理学、护理学、卫生护理或其他医学本科及以上学历。    • 四年及以上临床监查工作经验或相同经历，并且有项目管理（主管）相关经验；或五年及以 上临床监查工作经验或相同经历。 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 https://jobs.iqvia.com IQVIA 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.

Senior Clinical Research Associate 1 IQVIA is the Human Data Science Company oriented to drive human health outcomes forward. When you join IQVIA Spain as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers. With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas. Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionCollaborating with experts at study sites and with client representativesQualifications: University degree in scientific discipline or health careAt least 2 years of on-site monitoring experienceGood knowledge of clinical research regulatory requirementsVery good computer skills including MS OfficeExcellent command of Spanish and English languageOrganizational, time management and problem-solving skillsAbility to establish and maintain effective working relationships with coworkers, managers, and clientsFlexibility to travelDriver’s license class BWhat you can expect: Resources that promote your career growthLeaders that support flexible work schedulesPrograms to help you build your therapeutic knowledgeBetter Work-Life balance, optimal DOSExcellent working environment in a stabile, international, reputable companyMobile phone and attractive benefits packageIQVIA 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 https://jobs.iqvia.com. IQVIA 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. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.

Een afwisselende job in het veld, veel autonomie en ruimte om je enthousiasme te tonen? Ontdek jouw volgende uitdaging als medisch vertegenwoordiger. Regio Waasland: Antwerpen L.O., Edegem, Wilrijk, Dendermonde, St Niklaas, Beveren, Puurs, Lokeren. Wat houdt de job in? Je bezoekt huisartsen en specialisten en informeert hen over het productportfolio in cardiologie, reumatologie en pediatrieAnalyseer, plan en behaal je doelstellingenIdentificeer de belangrijkste artsen in je doelgroepVerwerk en analyseer de feedback van de artsenNeem deel aan seminaries, teamvergaderingen en cycle meetingsWat breng jij mee? Een (para)medisch Bachelor of Master diplomaJe preekt perfect Nederlands, woont in de regio en je beschikt over een rijbewijs BJe bent positief, enthousiast leergierig, flexibel en klantgerichtJe communiceert vlot en je staat open voor veranderingWat hebben we jou te bieden? Contract onbepaalde duur met optie tot integratie bij de klantCompetitief salaris afgestemd op jouw ervaringAantrekkelijk pakket aan extralegale voorwaarden (inclusief bedrijfswagen + laadkaart, groeps- en hospitalisatieverzekering, ..)Uitdagende functie met veel autonomieBegeleiding en opleidingKlaar om impact te maken? Solliciteer nu! Of stuur je cv naar [email protected] #LI-MB1 #LI-CES #LI-DNP 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 https://jobs.iqvia.com IQVIA 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.

Role DescriptionWe are seeking an experienced Senior Data Engineer to join our AI team. In this role, you will lead the development and optimization of data infrastructure supporting our Agentic AI initiatives. You will collaborate with ML engineers, AI scientists, and product managers to architect, implement, and maintain robust data pipelines powering autonomous AI agents. As a senior member of the R&DS AI Innovation Program, you will help shape data strategy and ensure our data solutions scale to meet the demanding requirements of next‑generation AI systems. Key ResponsibilitiesMandatoryDesign, develop, and maintain scalable data pipelines and ETL processes supporting AI research and development.Design and maintain scalable data models (e.g., star schemas, feature‑ready datasets, semantic layers) for analytics, ML training, and agent workflows.Collaborate with AI scientists and engineers to gather data requirements and ensure availability and quality.Implement data governance and security measures to protect sensitive information.Establish observability, lineage tracking, and monitoring frameworks to detect anomalies, freshness issues, and operational failures.Implement data partitioning, indexing, and storage optimization techniques for large‑scale AI datasets.Monitor and troubleshoot data pipeline issues to ensure continuity and reliability.Stay current with emerging data engineering and AI technologies.Drive data platform reliability, scalability, and cost optimization across cloud‑based infrastructure.PreferredDesign and implement scalable, resilient data architectures for AI agent training, fine‑tuning, and inference workflows.Build streaming and event‑driven pipelines enabling real‑time agent feedback, telemetry, and adaptive learning.Develop and maintain high‑performance pipelines using modern orchestration frameworks to support real‑time agent interactions.Create specialized storage and retrieval systems for vector embeddings, knowledge graphs, and symbolic reasoning components.Implement automated data validation, schema testing, and quality checks ensuring reliable AI training datasets.Implement comprehensive monitoring and governance frameworks ensuring high‑quality training data and compliance with privacy regulations.Continuously optimize system performance with a focus on reducing latency for agent decision‑making.QualificationsEducation Bachelor’s or Master’s degree in Computer Science, Data Engineering, or a related field; advanced degree preferred.Experience 5+ years of professional experience in data engineering, including at least 2 years focused on ML/AI data infrastructure.Programming & TechnologiesAdvanced proficiency in Python and Scala; experience with Rust, Go, Java, or Julia is valued.Expert‑level knowledge of SQL and NoSQL databases.Hands‑on experience with vector databases (e.g., Pinecone, Weaviate, Milvus).Proficiency with modern data orchestration platforms (e.g., Airflow 2.x).Cloud & InfrastructureExtensive experience with at least one major cloud platform (AWS, Azure, or GCP).Expertise in containerization and orchestration (Docker, Kubernetes).Experience with Infrastructure as Code tooling (e.g., Terraform).Data ProcessingExperience with distributed computing frameworks (Spark, Dask, Ray).Proficiency with streaming technologies (Kafka, Flink).Knowledge of modern data lakehouse architectures.Preferred QualificationsCertifications in cloud platforms, big data technologies, engineering, or ML operations.Experience collaborating with ML engineers on CI/CD pipelines for data processing and model deployment.Working knowledge of ML frameworks (PyTorch, TensorFlow).Experience with feature stores and experiment‑tracking platforms.Understanding of LLM fine‑tuning data requirements and processing.Experience developing data systems for autonomous AI agents or agentic AI applications.Background in prompt engineering or retrieval‑augmented generation systems.Experience with semantic caching and efficient storage/retrieval of AI‑generated artifacts.Familiarity with LLM evaluation metrics and benchmarking frameworks.Expertise in hybrid architectures combining traditional databases with vector stores.Experience with RAG systems and related data pipelines.Knowledge of RLHF data workflows.Experience mentoring junior engineers, establishing best practices, and contributing to architectural decisions.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 https://jobs.iqvia.com IQVIA 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. The potential base pay range for this role, when annualized, is 155 600,00 zł - 289 200,00 zł. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.