Role Description UnitedHealthcare’s Medical Policy team seeks a skilled and experienced epidemiologist to support the development and maintenance of medical policies. This individual will be responsible for researching the medical literature and summarizing relevant scientific articles for the medical policies in collaboration with a clinical policy writer and medical director and maintaining them over time using the latest published evidence. The ideal candidate will have experience in literature search, in critical review of the clinical literature, in summarizing evidence into medical policies or similar documents, in close multidisciplinary collaborations, and in process innovation and improvement. You’ll enjoy the flexibility to work remotely from anywhere within the U.S. as you take on some tough challenges. Primary Responsibilities: - Search the literature for scientific evidence - Critically appraise and summarize published evidence - Develop and maintain medical policies - Serve as a key resource on complex and/or critical evidence reviews (e.g. methods, interpretation) - Contribute to cross functional discussions related to research topics - Present findings in both small and large group settings - Collaborate with a larger team of medical policy writers, physicians, policy publication, and implementation experts to drive policy quality - Support continuous refinement and evolution of the medical policy development and maintenance process to drive industry-leading quality, top-of-talent work, and optimal use of modern content development and publication tools Qualifications - 2+ years of experience critically evaluating and synthesizing academic or scientific literature with demonstrated ability to identify methodological flaws, biases, or gaps in research - 2+ years of experience in writing medical policies or similar scientific documents, such as systematic reviews - Excellent knowledge of biostatistics, clinical epidemiological methods, and outcomes research - Proficiency in Microsoft Applications and working in shared document environment - Demonstrated ability to work with minimal supervision - Proven excellent medical writing skills/ability to write clearly for a diverse audience - Proven excellent written and verbal communication skills including the ability to present information to large audiences - Proven solid interpersonal skills and the ability to work collaboratively with a large and diverse team - Proven proactive attitude with a willingness to learn, innovate, and adapt in a fast-paced setting Requirements - 2+ years of hands-on experience applying the GRADE methodology to assess the quality of evidence and strength of recommendations in biomedical literature reviews - Experience using citation management software (e.g., EndNote, Zotero), Microsoft Excel and Word, and cloud-based collaboration tools such as SharePoint or Dropbox in a professional or academic environment - Research experience in clinical medicine - Experience in payer, managed care, health insurance, or clinical settings - Healthcare Policy writing experience Benefits - Comprehensive benefits package - Incentive and recognition programs - Equity stock purchase - 401k contribution (all benefits are subject to eligibility requirements) Application Deadline This will be posted for a minimum of 2 business days or until a sufficient candidate pool has been collected. Job posting may come down early due to volume of applicants.

Title: Senior Epidemiologist, Inflammation, IBD (FSP Sponsor Dedicated) Location: Durham, United States of America Full time Home-based R1544308 Job Description: Location: Remote, candidates must be US-based 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. 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.

Senior Epidemiologist, Inflammation, External Comparator Expertise (FSP Sponsor Dedicated) Location: - Wayne, NJ - Durham, NC - Boston, MA - Minneapolis, MN - New York, NY - San Francisco, CA Full-time Remote Job Description: 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: IQVIA is seeking an accomplished epidemiology leader to drive the design and execution of innovative real-world evidence (RWE) strategies for a leading sponsor organization. This senior role combines scientific rigor with strategic influence, enabling you to shape high-impact observational research that informs clinical development, regulatory decisions, and market access. Responsibilities: Study Lead: Lead execution of studies to generate actionable RWE within agreed timelines, budgets, and quality standards. Focus areas include but not limited to: - External comparators - Natural history of disease - Treatment patterns and switching - Comparative safety/effectiveness Epidemiology Leadership: Design and drive development of study protocols, statistical analysis plans, and study reports addressing priority methodological questions. Data Strategy: Conduct feasibility and assessment of fit-for-purpose real-world data (RWD) sources (claims, EHR, registries) to enable timely execution of RWE initiatives. RWD expertise: Construct cohorts, validate key variables, and guide implementation of descriptive and comparative analyses using RWD for complex research questions. Stakeholder Engagement: Build strong partnerships with internal teams, external vendors, and sponsor stakeholders to ensure alignment and delivery of strategic objectives. 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. This is a remote role. Candidates must be based in the US. 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, 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.

Role Description Amazon Integrated Security is seeking a Principal Applied Scientist to lead research at the intersection of cognitive psychology, measurement science, and AI security. This role will pioneer new approaches to understanding and leveraging behavioral characteristics of autonomous AI systems in security contexts, turning threat actor use of AI into a structural advantage for defenders. - Establish and lead a novel research program exploring cognitive patterns and biases in agentic AI systems used for offensive security purposes. - Design and conduct experiments to understand black-box AI system behavior. - Develop measurement frameworks for previously unmeasurable security concepts. - Translate research findings into actionable defensive strategies and tooling. - Create feedback loops between offensive and defensive security teams. - Collaborate with threat intelligence experts and red team operations. - Publish findings that advance both academic understanding and practical security outcomes. - Apply measurement science expertise to quantify complex security concepts including risk, business impact, and trust. A day in the life: - Work closely with a Principal Technologist with AI and security expertise, senior security engineers with threat intelligence backgrounds, offensive AI security teams, and detection/response operations. - Mentor junior scientists and engineers while maintaining strong connections with academic research communities. Qualifications - PhD in Cognitive Psychology, Measurement Science, Human Factors, or a related field. - 5+ years of post-doctoral research experience. - Track record of scientific contributions demonstrated through publications, patents, or shipped products. - Experience designing and conducting experiments to understand complex system behavior. - Experience translating research findings into practical product or operational improvements. Requirements - Deep expertise in experimental design and analysis for understanding black-box cognitive systems. - Proven ability to turn novel research into practical product decisions and operational improvements. - Excellent communication skills to translate complex research findings for technical and non-technical audiences. - Demonstrated success leading research programs that bridge multiple disciplines. - Strong publication record in top-tier venues. - Experience working in ambiguous problem spaces with high uncertainty. - Familiarity with AI/ML systems, security operations, or threat intelligence. Company Description Amazon is an equal opportunities employer. We believe passionately that employing a diverse workforce is central to our success. We make recruiting decisions based on your experience and skills. We value your passion to discover, invent, simplify and build. Protecting your privacy and the security of your data is a longstanding top priority for Amazon. Please consult our Privacy Notice to know more about how we collect, use and transfer the personal data of our candidates. Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status. Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit our accommodations page for more information.