Overview Join to apply for the Associate Biostatistics Director - FSP (Permanent Home-based) role at IQVIA . Responsibilities Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions. Influence and contribute to clinical development plans, collaborate with cross-functional team for governance reviews. Lead statistical strategy for planning and study execution (member of Study Executive Team, Clinical Development Team) and quantitative evaluation to clinical trials, regulatory submissions, and related documents. Provide statistical thought partnership for innovative study design and clinical development plans, including Go-No Go criteria and probability of technical success calculations. Provide for project-wide planning of analyses; quality and timely delivery of interim and final results, including integrated analyses for submissions. Represent Biostatistics in interactions with regulatory authorities (eg, FDA, EMA, PMDA). Be responsible for interpreting analysis results and ensuring reporting accuracy in study reports and regulatory documents. Prepare abstracts, posters, oral presentations and written reports to effectively communicate results of clinical programs and studies to internal and external stakeholders and colleagues with varying levels of clinical research knowledge. Education PhD or MS in Biostatistics, Statistics or related field Experience Minimum of 8 years of experience in clinical trial statistics, preferably within a pharmaceutical or CRO setting. Technical Expertise: Advanced proficiency in SAS / R for data analysis and statistical programming. Experience with Bayesian methods, predictive modeling, and simulation techniques. Proven track record in strategic study design, including adaptive designs, sample size calculations, and interim analysis planning. Familiarity with regulatory guidance on statistical methodologies (e.g., FDA, EMA, PMDA). Solid experience in applications of advanced statistical methodologies Leading roles in regulatory submissions Experience in interactions with major regulatory authorities preferred Demonstrated statistical expertise and leadership in facilitating and optimizing the (pre/early/full-) clinical development strategy Study Design and Strategy: Ability to lead statistical discussions during protocol development and study planning. Skilled in defining statistical analysis plans (SAP) and developing strategic approaches for complex study designs. Experience in strategy discussions involving adaptive design, go/no-go criteria, and futility analyses. Collaboration and Communication: Strong communication skills to effectively present statistical concepts to cross-functional teams. Proven experience in collaborating with clinical and regulatory teams to align statistical strategy with overall program objectives. Company 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 #J-18808-Ljbffr
Apply for the DM/STDM Programmer role at IQVIA . Location: Remote (UK, Spain, South Africa, Hungary, Ireland, Italy, Portugal, Czech Republic, Bulgaria, Belgium). Role Overview: This unique role within IQVIA lends itself to a technically minded Project Manager with strong communication skills and SDTM knowledge. Having experience with SAS programming will also be a huge benefit. The role can be based remotely from anywhere in Europe or in South Africa. This role is part of a sponsor dedicated project where you will be working with the client directly to manage Database Delivery from external vendors. The primary functions of this role will be to build study eCRFs in Formedix Ryze (Certara), define structures of datasets that are part of data transfer specifications and ensure quality and completeness of SDTM format data. Primary Functions Build study eCRFs in Formedix Ryze (Certara) Define dataset structures for data transfer specifications Ensure quality and completeness of SDTM format data Main Responsibilities Collaborate with Sponsor colleagues and CRO Partners to finalize the design, creation, and implementation of EDC solutions. Work with Study Data Leads to plan for data receipt and oversee it throughout clinical trials. Process data loads from various sources into clinical and operational data repositories, including reviewing and communicating issues. Program reports and contribute to the standardization of processes and reports for data review and analysis for external partners/vendors and internal teams. Complete formal and ad-hoc analyses and oversight of SDTM data. Review critical documents/deliverables (SDTM Annotation, SDTM datasets) to ensure consistent use of Data Standards and support the creation of DE datasets. Attend meetings with various teams (Mission, Submission, Project, Program, JCST, DEM, Biometrics, Clinical & Regulatory Solutions Team (CRST), Early Phase) Perform quality checks and create standard edit checks for new CRF modules. Support audits and inspections as required and handle other responsibilities and projects assigned by the Company. Experience Required Substantial experience in relational database design. Substantial experience with SAS programming preferred. Experience with Data Management processes, including Review of SDTM annotated CRFs, Writing and reviewing technical specifications, Reviewing log files for errors and warnings, Resolving/troubleshooting errors, Data mapping and SDTM Controlled Terminology. Prior experience in a clinical or pharmaceutical-related field. Prior experience in a Data Management-related field. Experience with relational databases, preferably Clinical Data Management and EDC Systems. Advanced familiarity with reporting tools. Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices. Excellent command of English, both verbal and written. 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 . #J-18808-Ljbffr
Overview IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical programming needs in our DS3 environment (home based). Responsibilities Import data from various sources Program quality control checks for source data and reporting data issues Interpret project level requirements and develop programming specifications Write programming code following established Good Programming Practices Program SDTM and ADaM datasets Program to create statistical analysis tables, listing and figures Validate datasets and all statistical outputs per prescribed gate checks Communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and timelines Use and promote the use of established standards, SOPs, and standard methodologies Export data and clinical study report materials Provide training and mentoring to team members and department staff You can help us bring clinical trial statistical analysis into the next generation. Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects across therapeutic areas. Be challenged in a fast-paced team environment that is collaborative in performing biostatistical analyses and advanced statistical programming. Development opportunities and mentoring at all levels enable you to progress your long-term career in the direction you choose. The Person We know that meaningful results require not only the right approach, but also the right people. Candidates should possess a Master’s or Bachelor’s degree in Biostatistics, Statistics, Mathematics, or Computer Science, and have a strong educational or practical evidence in programming. Key required skills include: Home Based/Remote 5+ experience in Statistical Programmer role from CRO/Pharma with ADaM/SDTM/ TLFs Excellent accuracy, attention to detail, problem solving, organizational as well as interpersonal communication. Experience in programming in SAS within the CRO/Pharma/Biotech/Healthcare industries Knowledge of statistics and exhibit routine and occasionally complex analytical skills A focus on quality, accuracy, and completeness of work activities Excellent communication skills A good understanding of Good Clinical Practice and ICH guidelines Ability to independently lead (or have lead potential) and estimate programming scope of work, handle resource assignments, communicate work status, and work within project timelines for deliverables Take initiative and can be counted on to get the job done, with integrity Have the self-awareness to recognize when negotiating skills and assistance are needed Ability to establish and maintain effective working relationships with co-workers, managers, and clients Embrace your curiosity and grow your career in an exciting environment where development is a priority. Think boldly and disrupt conventional thinking. Enjoy what you do. Discover a career with greater purpose and help create a healthier world. #LI-remote Whatever your career goals, we are here to ensure you get there! This role is not eligible for UK visa sponsorship IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled #J-18808-Ljbffr
Senior Global Trial Manager – Single Sponsor (Novartis) Are you experienced in managing late phase clinical trials at a global level? We are looking for a Senior Global Trial Manager to join our Single Sponsor Department , dedicated exclusively to Novartis . Join our global team and take ownership of delivering late-phase clinical trials that meet timelines, budgets, and quality standards. As a core Clinical Trial Team (CTT) member, you\'ll lead critical aspects of global studies and collaborate across functions to drive success. As part of your role, you’ll have the opportunity to specialise in one of the following areas: Scientific Review Committee (SRC) Non-Interventional Studies (NIS) Managed Access Programs (MAP) Investigator-Initiated Trials (IITs) Research Collaborations (RCs) Program Level Documents (PLD) Key Responsibilities Clinical Documentation & Study Tools Draft sections of protocols, CRFs, training materials, and data review plans Contribute to the development of safety updates, IBs, and regulatory submissions Project Leadership Oversee data review and TMF audit readiness Forecast/manage investigational product supply Support study closeout, issue resolution, and lifecycle budget tracking Contribute to Managed Access Program coordination and compliance Vendor & Stakeholder Management Coordinate CRO/vendor selection and performance Facilitate advisory boards (DMCs/Steering Committees) and serve as the site liaison Lead cross-functional collaboration with data management, drug supply, and more What You'll Bring Advanced degree in life sciences or healthcare 2–5 years\' global experience managing phase IV, PASS, PAES, or NIS trials Strong track record in protocol development, study startup, and regulatory writing (e.g. PSURs, DSURs, NDA/BLA reports) Excellent communication, organizational, and collaboration skills Deep understanding of GCP and clinical trial design Passion for advancing real-world evidence and patient outcomes This role is not eligible for UK VISA sponsorship. EEO Minorities/Females/Protected Veterans/Disabled #J-18808-Ljbffr
Overview We are seeking an experienced Director, Compensation & Benefits (EMEA) to join our Centre of Excellence on a fixed-term contract . This role provides critical leadership and continuity for our regional C&B agenda, ensuring competitive, compliant, and cost-effective programs across EMEA. You will lead major compensation and benefits initiatives , partner with senior HR and business leaders, and deliver strategic projects that shape our Total Rewards offering. This is a hands-on role requiring strong technical expertise, stakeholder influence, and the ability to navigate complex, multi-country environments. Key Responsibilities Lead Benefits Strategy & Delivery Own and evolve the EMEA benefits strategy, balancing cost competitiveness, cost management, and evolving market needs. Drive Benefits Process Optimization Lead in continuous improvement initiatives to enhance operational efficiency and effectiveness within the HR Centre of Excellences. Client Focus and Stakeholder Engagement Serve as a strategic partner and subject matter expert to senior HR Partners, Finance, and business leaders on complex benefits and compensation-related issues by delivering clear, data-driven recommendations. Data Driven Insights Drive the use of data and analytics to uncover insights that guide strategic direction, evaluate program impact, and support informed decision-making. Compensation Program Leadership Support in the delivery of the annual salary planning and bonus processes in EMEA; ensure alignment with global frameworks and local statutory requirements. Team Leadership Coach and develop a high performing team, fostering a culture of excellence and collaboration, ensuring capability to deliver on strategic priorities. Governance & Compliance Ensure compliance with local legislation, regulations and internal policies while maintaining up-to-date knowledge of evolving EU directives. M&A Due Diligence Provide expert analysis, insight and recommendations during due diligence to align compensation and benefits programs. What You’ll Bring Experience: 9+ years in Compensation & Benefits, with proven leadership in matrixed, multi-country environments. Expertise: Deep knowledge of global compensation and benefits practices, including harmonization, budgeting cycles and policy redesign. Strategic & Analytical Skills: Ability to interpret market data, model costs, and influence decisions at senior levels. Project Leadership: Track record of delivering complex initiatives across regions with a high degree of involvement in delivery and leading a project team. Collaboration: Strong consultative skills and ability to influence and partner effectively across HR, Finance, and business stakeholders. Technical Fluency: skilled in using Excel, Power BI, and emerging technologies such as Generative AI for data analysis, reporting and strategic decision-making. Education: Bachelor’s degree required; advanced certifications (e.g., CCP) preferred. Why Join Us? This is an opportunity to shape the future of Total Rewards in EMEA , working on high-impact projects such as benefits harmonization, cost optimization, and strategic compensation planning. You’ll join a collaborative team that values innovation, operational excellence, and employee well-being. 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 a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled #J-18808-Ljbffr
Biotech Client Partner – Regulatory, Drug Development, Clinical, Consulting and Real-World Strategy, EMEA Role Overview As a Biotech Client Partner you will support on selected clients from the point of view their asset development and build relationships with C-level stakeholders. The focus will be on the crafting of solutions including (but not limited to) Regulatory and Drug Development strategy, Clinical development, consulting, analytic services, Real World Evidence and elements of Technology. This role will operate across the client organization, particularly with senior global stakeholders to define and execute our priorities to move the client business forward, providing the conduit between the client and the rest of IQVIA. This role forms one of the key client roles and should closely partner with the Account Directors from multiple departments including but not limited to Research and Development Solution (RDS), Real World Evidence (RWE), Commercial services, Patient Centric Services, Technology and laboratories to drive the account forward in accordance with both short-term priorities and long-term vision. This role also requires a close interaction with the project execution team and oversight of the different department involved to consolidate the development of a close relation with the client, facilitating a smooth project delivery and repeat business. Responsibilities Drive overall business growth globally with a focus on increasing sales, revenue, and profitability into the assigned global account and assigned target assets. Support the development of the Clinical, Regulatory and Drug Development Solutions, Real World & Medical Affairs account asset strategy with input from the broader account aligned team and orchestrate the operational execution including selection and planning around assets. Align the account asset strategy with RDS, Regulatory, Drug Development & RWE to ensure a joined up ‘Molecule to Market’ engagement. Build long term relationships with Executive leaders within the client to ensure long term revenue growth for RDS, Regulatory, Drug Development and RWE Leverage your existing external network to gain referrals and facilitate establishment of a trust with your clients Influence the client’s strategy and position IQVIA through thought leadership and innovation aligned to client strategic asset priorities. Leverage senior IQVIA resources and subject matter experts as needed in building preferred supplier relationships. Proactively engage client C-level leaders by anticipating client needs and leveraging the IQVIA cross departmental expertise to develop both short- and long-term cross functional solutions. Our Ideal Candidate Proven expertise across the Biotech, Pharma, and Life Sciences drug development lifecycle—including medical, pre-clinical, clinical operations, and regulatory domains. Strong understanding of Biotech business strategy and operational processes, gained within a professional services environment (CRO). Solid Consulting background with a track record of delivering client-focused solutions. Well-connected within the Biotech ecosystem, with an extensive external network. A natural relationship builder and influencer, able to engage stakeholders across all levels. Skilled in consultative selling, with the ability to uncover client needs and orchestrate cross-functional teams to deliver compelling, tailored solutions. Comfortable engaging with senior executives and navigating complex client environments. Experienced in solution development—able to craft persuasive narratives, generate bold ideas, and back them with evidence. Strong collaboration, influence, and persuasion capabilities. Adept at operating within complex matrix organizations, aligning diverse stakeholders. Demonstrated success in selling and negotiating large-scale, cross-functional solutions. Brings excellent communication, organizational skills, analytical thinking, and problem-solving ability. Why Join? 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 fitting personality . 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 is 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 a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled #J-18808-Ljbffr
Hospital Account Manager Location: Republic of Ireland - North Field-Based Role | Full-Time | Competitive Salary + Benefits Are you a strategic and driven professional with a passion for healthcare innovation? We are seeking an experienced Hospital Account Manager to lead engagement and growth across hospital accounts in Ireland, focusing on a cutting-edge portfolio. This role is ideal for someone who thrives in a dynamic environment, excels at building relationships with healthcare professionals, and is motivated by delivering impactful solutions in cardiology, nephrology, and ophthalmology. Key Responsibilities Develop and manage relationships with hospital stakeholders, cardiovascular consultants, and clinical teams to drive growth and engagement. Identify new business opportunities and ensure high levels of customer satisfaction. Deliver against national sales targets and performance metrics. Analyse sales data to create actionable weekly, monthly, and quarterly plans. Maintain accurate records in CRM systems, prioritising key opportunities. Collaborate with internal teams to execute targeted marketing campaigns and educational initiatives tailored to the Irish market. Lead commercial negotiations, including pricing and contract agreements. Provide market insights to support strategic planning and national tender submissions. Work cross-functionally with sales, finance, clinical geneticists, and lab operations to ensure seamless customer delivery. Ensure compliance with all relevant policies, ethical standards, and regulatory frameworks. Qualifications & Experience Degree in Life Sciences or a related discipline. Proven experience in cardiology is essential. Minimum 5 years’ experience in pharmaceutical or healthcare sales, with a strong track record of business development. Knowledge or experience in genomics is an advantage. Strong communication, organisational, and interpersonal skills. Ability to influence stakeholders and collaborate across teams. Willingness to travel across Ireland. Proactive, self-motivated, and results-oriented. Resilient and adaptable in a fast-paced environment. Strategic thinker with a customer-first mindset. Ethical and collaborative team player. Ready to make a difference in healthcare? Apply now to join a dynamic team transforming patient care through innovation and strategic partnerships. Please note: Sponsorship is not available for this opportunity. Candidates attend interviews at their own cost. Expenses incurred to attend an interview are not covered by IQVIA. EEO Minorities/Females/Protected Veterans/Disabled #J-18808-Ljbffr
Social network you want to login/join with: ? Field-based across Carlow, Kildare, Laois, Wicklow, Offaly, Westmeath, Kilkenny & Wexford Are you a seasoned pharmacy sales professional with a passion for healthcare and a business-owner mindset? We’re looking for a resilient, driven, and strategic Pharmacy Sales Representative to champion leading consumer healthcare brands across the Midlands. You’ll be the face of innovation, building strong relationships with pharmacy stakeholders, driving sales, and delivering impactful campaigns that make a real difference to customers and communities. What You’ll Do: Own your territory and drive brand uptake through smart, data-driven account planning. Build lasting partnerships with pharmacies, delivering value through education, promotions, and commercial excellence. Collaborate cross-functionally to unlock growth opportunities and overcome market challenges. Be a role model for ethical business practices and agile decision-making. What You’ll Bring: 5+ years of pharmacy-level experience in consumer healthcare. A degree in Business, Marketing, Science or related field. Exceptional communication, negotiation, and planning skills. A valid driver’s licence and the flexibility to travel. Why Join Us? Be part of a team that’s shaping the future of pharmacy sales. We’re committed to innovation, integrity, and impact—and we’re looking for someone who’s ready to make their mark. Ready to take the next step? Apply now and bring your energy, expertise, and entrepreneurial spirit to this exciting opportunity. Please note: Sponsorship is not available for this opportunity. Candidates attend interviews at their own cost. Unfortunately, expenses incurred to attend an interview are not covered by IQVIA. #LI-DNI #LI-CES #LI-LK1 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 #J-18808-Ljbffr
Social network you want to login/join with: Field-Based Role | Full-Time | Competitive Salary + Benefits Are you a strategic and driven professional with a passion for healthcare innovation? We are seeking an experienced Hospital Account Manager to lead engagement and growth across hospital accounts in Ireland, focusing on a cutting-edge portfolio. This role is ideal for someone who thrives in a dynamic environment, excels at building relationships with healthcare professionals, and is motivated by delivering impactful solutions in cardiology, nephrology, and ophthalmology. Key Responsibilities Develop and manage relationships with hospital stakeholders, cardiovascular consultants, and clinical teams to drive growth and engagement. Identify new business opportunities and ensure high levels of customer satisfaction. Deliver against national sales targets and performance metrics. Analyse sales data to create actionable weekly, monthly, and quarterly plans. Maintain accurate records in CRM systems, prioritising key opportunities. Collaborate with internal teams to execute targeted marketing campaigns and educational initiatives tailored to the Irish market. Lead commercial negotiations, including pricing and contract agreements. Provide market insights to support strategic planning and national tender submissions. Work cross-functionally with sales, finance, clinical geneticists, and lab operations to ensure seamless customer delivery. Ensure compliance with all relevant policies, ethical standards, and regulatory frameworks. Qualifications & Experience Degree in Life Sciences or a related discipline. Proven experience in cardiology is essential. Minimum 5 years’ experience in pharmaceutical or healthcare sales, with a strong track record of business development. Knowledge or experience in genomics is an advantage. Strong communication, organisational, and interpersonal skills. Ability to influence stakeholders and collaborate across teams. Willingness to travel across Ireland. Attributes for Success Proactive, self-motivated, and results-oriented. Resilient and adaptable in a fast-paced environment. Strategic thinker with a customer-first mindset. Ethical and collaborative team player. Ready to make a difference in healthcare? Apply now to join a dynamic team transforming patient care through innovation and strategic partnerships . Please note: Sponsorship is not available for this opportunity. Candidates attend interviews at their own cost. Unfortunately, expenses incurred to attend an interview are not covered by IQVIA. #LI-DNI #LI-CES #LI-LK1 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 #J-18808-Ljbffr
Job Title: Pediatric Nurse Location: Dublin We’re currently seeking Pediatric Nurses to join our Healthcare Professionals Network. IQVIA are looking for candidates who excel in customer care and have excellent personable skills. Experience in the following would be desirable: Commutable distance to do visits in Dublin Pediatric experience including pediatric phlebotomy In date NMC pin Willingness to travel Must have full driving license and use of a car Ideally an enhanced DBS and on the update service Join our team and make a difference in patients’ lives. Apply today! #LI-DNP #LI-CES #LI-HCPN #LI-CT1 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 #J-18808-Ljbffr
