• Support all aspects of execution of primary data collection research studies, including literature reviews; development of data collection instruments (e.g., surveys, interview guides); study protocols; data collection; data analysis and interpretation; and support dissemination activities. • Contribute to the development of project deliverables under the guidance of senior team members with methodological and subject matter expertise. • Assist with the delivery of project components by collaborating with team members to ensure high-quality outputs and help maintain project timelines for assigned tasks. • Support client engagement activities by drafting update slides for regular client meetings with guidance from senior team members, and documenting meeting notes, action items, and next steps. • Contribute to proposal and presentation development by drafting background sections, task descriptions, timelines, and references with guidance from senior team members.

• Support all aspects of execution of primary data collection research studies, including literature reviews; development of data collection instruments (e.g., surveys, interview guides); study protocols; data collection; data analysis and interpretation; and support dissemination activities. • Contribute to the development of project deliverables under the guidance of senior team members with methodological and subject matter expertise. • Assist with the delivery of project components by collaborating with team members to ensure high-quality outputs and help maintain project timelines for assigned tasks. • Support client engagement activities by drafting update slides for regular client meetings with guidance from senior team members, and documenting meeting notes, action items, and next steps. • Contribute to proposal and presentation development by drafting background sections, task descriptions, timelines, and references with guidance from senior team members.

Title: Epidemiologist, Senior Location: Remote, candidates must be US-based time type Full time job requisition id R1542028 Join IQVIA’s Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you’ll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA’s global expertise. Core Function Description: Design and conduct epidemiological studies to generate real-world evidence within time, budget, and quality standards, including but not limited to natural history of disease, population characterization, assessment of treatment patterns and unmet need, development of external comparators, benchmarking of clinical outcomes, comparative safety and effectiveness research, and post-authorization studies. Skill sets of the Epidemiologist role are similarly required, with the expectation of more experience, able to operate strategically under limited supervision, well versed in current Epidemiology research methods, deep understanding of how RWE fits within drug development, regulatory, medical, safety and other functions. Required Experience - Lead development of study protocols, analysis plans, and study reports to answer research questions of priority to RWE. - Lead, design, and manage epidemiological, biomarker and/or data science projects. - Lead, plan, design, and conduct analyses for internal and external decision making (e.g., responses to regulatory authorities, rapid analyses of safety queries). - Lead the identification of fit-for-purpose data for the timely execution of the RWE strategy. - Constructed cohorts using RWD sources (e.g., claims, EHR) and evaluate key variables, including diagnosis and procedures codes, and plan validation studies as needed. - Contribute to the communication of observational research results and methods, including development of pertinent sections of regulatory documents, reports, publications, white papers. - Support the effective communication of study/analysis results to support internal and external decisions. - Coauthor abstracts and manuscripts for external dissemination of methodologic study results. - Contribute to the development of processes and training aimed at increasing the efficiency, quality, and impact of functional activities. Technical Expertise: - Observational research methods (both Primary and Secondary), deep knowledge of biostatistics and analysis methods, understanding of regulatory processes. - Ability to design studies independently, (i.e., ability to translate research questions to create study design). Subject Matter Expertise: - Provide subject matter expertise and conduct analyses for descriptive and comparative research using RWD (examples include claims, EHR, PRO/COA, registry data) for methodologic research questions. - Deep, hands-on familiarity with EHR data curation behind health system firewalls, including practical knowledge of where key clinical outcomes are captured across data tables. - Expert knowledge and extensive experience with pharmacoepi methods (i.e., signal detection and validation methods). - Leverage RWE expertise to identify evidence gaps and develop options to address the evidence gaps in support of Clinical Development Programs. Minimum Qualifications - PhD in Epidemiology, Biostatistics, Psychometrics, or related field with a minimum of four (4) years of relevant post-doctoral experience, preferably in pharmaceutical industry, biotechnology, or consulting environment. Master’s degree in epidemiology, biostatistics, bioinformatics, or relevant scientific field, plus 7-9 years of experience in lieu of PhD may be acceptable. - Deep understanding of observational research methods and experience to support the design and conduct of observational research, including protocol, statistical analysis plan, and study report development. - Extensive knowledge of secondary data sources and experience with secondary data analysis, including electronic medical record and/or medical claims databases. - A record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation is preferred. - Demonstrated ability to function with an increasing level of autonomy and to develop productive cross- functional collaborations in a matrix environment. - Ability to manage priorities and performance targets. - Experience in leading drug development project for 2+ years for therapeutic area of assignment preferred. What’s in it for you? - Be part of a forward-thinking team that helps shape the next generation of evidence-based healthcare. - Work hand-in-hand with one leading sponsor, gaining deep expertise in their therapies. - Access IQVIA’s global network who supports your growth. This is your chance to make an impact, while building a career that matters. 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 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. 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. The potential base pay range for this role, when annualized, is $110,500.00 - $276,100.00. 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.

Title: Epidemiologist, Vaccines (FSP Sponsor Dedicated) Job Description: Location: Remote, candidates must be based in the US Join IQVIA's Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you'll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA's global expertise. Overview: The RWE/Epi Scientist provides scientific support for RWE/Epidemiology studies by conducting literature reviews, data cleaning, code look-ups, and quality control activities. The role also contributes to scientific deliverables and supports operational coordination across studies to ensure high-quality execution. Organizational Relationships - Reports to RWE/Epi Scientist within the Integrated Evidence Generation (IEG) organization - Collaborates with Medical Evidence Development (MED) colleagues, CMO colleagues (e.g., DS&A, Regulatory, Safety), Clinicians, HV&E/GAV partners, and other cross-functional scientific partners to lead operational activities - Interfaces with other external vendors to drive operational oversight Responsibilities: Scientific Responsibilities: - Conducts literature reviews, scientific summaries, data cleaning, code look up, and QC tasks - Contributes to development of abstracts, manuscripts, posters, and scientific summaries - Support creation of analysis planning documents and table shells, working closely with programmers - Provide rapid responses to epidemiology and safety information requests - Perform any other relevant scientific tasks as needed to support study progress Execution Coordination & Oversight: - Provides operational oversight across multiple studies or therapeutic areas - Maintain study documentation, trackers, and operational tools to ensure consistent process application - Coordinate safety requests, data requests, timelines, and other cross-functional operational needs - Supports development and management of study trackers, safety requests, and other operational resources - Monitor progress of vendor deliverables and help identify risks or delays Requirements: Education/experience: - PhD plus 2 years of professional epidemiology experience, or Master's degree (MPH minimum) plus 5 years of professional epidemiology experience - Pharma epidemiology experience preferred - Experience in applied epidemiology or scientific operations - Experience working in a matrixed, cross-functional team environment - Experience supporting development of scientific deliverables Skills: - Strong quantitative and analytical skills required - Database and observational study experience required - Experience with AI is preferred What's in it for you? - Be part of a forward-thinking team that helps shape the next generation of evidence-based healthcare. - Work hand-in-hand with one leading sponsor, gaining deep expertise in their therapies. - Access IQVIA's global network who supports your growth This is your chance to make an impact, while building a career that matters. 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. 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 $110,500.00 - $276,100.00. 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.