Role Description We are seeking a talented professional to carry out projects in imaging AI, informatics, health information technology and data science. The Research Data Curator will be responsible for collecting, processing and publishing medical imaging and related information for use in research. - Manage collection, curation and maintenance of imaging data and related resources for AI research efforts. - Oversee RSNA data ingestion tools and processes to organize, manage and prepare data submitted by contributing sites for publication. - Provide consultation to data contributing sites regarding data submission requirements, processes and tools. - Investigate and advise RSNA staff on platforms and tools for research data publication. - Report regularly to Director of Informatics, project teams, oversight committees and collaborating organizations on project status, progress and issues. - Research and evaluate new technologies to support project work. Qualifications - BS or equivalent with preference for medical informatics or related technical field. - Two years or more of direct AI, medical imaging or informatics project experience preferred. - Experience working with medical imaging and other clinical data. - Problem solving ability and project management skills. - Detail oriented with excellent organizational skills. - Ability to work effectively in collaboration with staff and volunteers. - Self-directed with personal initiative and good judgment. - Strong written and oral communication skills. Requirements - To apply, you should include a CV and a cover letter describing your scientific background and interest in editorial and evaluative roles in scholarly publishing. - While some roles may require proximity to our Oak Brook, IL office, roles based outside of our Oak Brook, IL office can sit in any of the following states: AZ, CA, FL, GA, IL, IN, KS, MD, NC, NY, OH, OR, TX, VA, VT, WA, WI and Washington, D.C. - Please only apply if you are able to live and work full-time in one of the states listed above. - State locations and specifics are subject to change as our hiring requirements shift. - All salaried ranges are standardized nationwide and will not vary by region. Company Description The Radiological Society of North America is an equal opportunity employer and prohibits discrimination and harassment of any kind. RSNA is committed to hiring and employing qualified people without regard to race, color, religion, sex, marital status, national origin, age, disability, veteran status, citizenship status, genetic information, sexual orientation, unfavorable military discharge, ancestry, order of protection status, pregnancy, or any other legally protected characteristic. All employment decisions at RSNA are based on business needs, job requirements, and individual qualifications.

• Manage each of the data management projects to which assigned; provide leadership to the corresponding data management teams. • Represent WCT in all dealings with Sponsors with respect to the Data Management aspects of the projects to which assigned. • Liaise with the Director, Data Management at regular intervals to discuss progress and any issues outstanding. • Take responsibility for staff training for all projects to which assigned; both direct involvement in training and supervision of staff assigned to training. • Ensure that all data management operations are conducted to WCT SOPs; contribute to the ongoing revision/improvement of these SOPs. • Create and review project specific documentation for assigned trials, i.e. the Data Management Plan and the Data Management File. • To ensure that adequate QC checks (including spot checks) and Database Quality Assessments on the clinical databases of assigned projects.

Career Category Research Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Bioanalytical Portfolio Scientist What you will do Let’s do this. Let’s change the world. In this vital role you will serve as the technical subject matter expert for outsourced methods and is responsible to ensure adequate method validation and optimal method performance at CROs. The Bioanalytical Portfolio Scientist is responsible for oversight of the outsourced bioanalytical phases of studies governed by applicable GLP/GCP principles. Individuals in this role will provide scientific and technical oversight of bioanalytical activities (including pharmacokinetic [PK] and toxicokinetic [TK] analyses) performed by external contract research organizations (CROs), ensuring adherence to validated methods, data integrity standards, and alignment with study protocols and regulatory requirements. The ideal candidate will have a strong background of method development, validation, and troubleshooting in quantitative ligand-binding assays (LBA) and/or LC-MS bioanalysis, combined with excellent communication skills. This role is well suited for scientists who seek to learn more about externalized work and who thrive working with others in a collaborative manner. - Provides scientific and technical oversight for the transfer, validation, and execution for pharmacokinetic (PK) assays, ensuring adherence to sponsor requirements and current regulatory guidance on bioanalytical assays (e.g. FDA, ICH, EMEA, NMPA) - Leads the transfer and validation of PK assays at external CROs using ligand-binding, ELISA, ECL, LC-MS/MS and hybrid methodologies - Collaborates closely with internal bioanalytical subject matter experts to understand critical attributes of the PK method to ensure successful assay transfer and validation - Monitors assay performance over time and provides input for troubleshooting and continuous improvement efforts - Accountable for method lifecycle management, including review of method validation plans, protocols, reports, and qualification/bridging of reagents and reference material - Reviews analytical data, method protocol, validation/sample analysis plans, reports, and other study documentation for scientific accuracy and consistency with GLP/GCP documentation standards and current regulatory guidance - Works with cross functional partners from CROs to navigate issue resolution and escalation utilizing the governance structure - Provides subject matter expertise during supplier evaluation and monitoring activities - Follows and contributes to guidance documents and SOPs What we expect of you We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a scientist with these qualifications. Basic Qualifications: - Doctorate degree OR - Master’s degree and 2 years of regulated commercial scientific laboratory experience OR - Bachelor’s degree and 4 years of regulated commercial scientific laboratory experience OR - Associate’s degree and 8 years of regulated commercial scientific laboratory experience OR - High school diploma / GED and 10 years of regulated commercial scientific laboratory experience Preferred Qualifications: - Excellent communication skills - Strong project management experience - Fluency in English, both in written and oral communication - Demonstrated expertise in PK assay development, validation, and troubleshooting for LBA, LC-MS or hybrid assays - Knowledgeable on current relevant regulatory guidance/regulations (e.g. FDA, ICH, EMEA, NMPA) - Experienced in working with CROs - Project and people management - Process management and planning skills - Excellent written and verbal communication skills - Collaborates, negotiates and persuades others, both internally and externally - Openly promotes cooperation across the organization - Project and issue management skills - Drives for results; delivers processes and outcomes of the highest quality - Consistently communicates in a manner that is appropriate to the situation What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is $xxx,xxx.00 to $xxx,xxx.00. Actual salary will vary based on several factors including, but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: - A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts - A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan - Stock-based long-term incentives - Award-winning time-off plans - Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies. Apply now and make a lasting impact with the Amgen team. careers.amgen.com In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. Sponsorship Sponsorship for this role is not guaranteed. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. .Salary Range 109,020.15USD -147,497.85 USD

Where You’ll Work Virginia Mason Franciscan Health has a rich history of providing exceptional healthcare, dating back to 1891. Building upon a legacy of compassionate care and innovation, our organization has evolved over the years through strategic partnerships and integrations to expand our reach and services across the Puget Sound area.Today, as Virginia Mason Franciscan Health, we remain deeply committed to healing the whole person – body, mind, and spirit – in the communities we serve. This commitment is strengthened by the diverse expertise and shared values brought together through our growth.Our dedicated providers offer a full spectrum of health care services, from routine wellness to complex disease management, all grounded in rigorous research and education. Our comprehensive network of 10 hospitals and nearly 300 care sites strategically located across the greater Puget Sound region reflects our ongoing commitment to accessibility and comprehensive care.We are proud of our pioneering medical advances and numerous awards and accreditations that reflect our dedication to excellence. When you join Virginia Mason Franciscan Health, you become part of a team that delivers top-quality, professional healthcare in modern, well-equipped facilities, and contributes to a legacy of service built on collaboration and shared purpose. Job Summary and Responsibilities This job is responsible for staffing/leading collaborative efforts to design, develop, test, implement and maintain data modeling and analytics solutions for use in clinical, quality and population health improvement. Work includes representing data in contexts to include reports, dashboards, quantitative analytic models and interactive analysis tools. An incumbent will conceptualize and develop analytic solutions to help address Virginia Mason Franciscan Health's (VMFH) complex challenges using a variety of data science, analytic techniques, and tools. Work includes anticipating and supporting the information needs of VMFH clinical and business partners, enabling data-driven decision-making, and contributing to a culture of collaborative analytics throughout the organization. Working with front-line clinicians, administrative leaders and information systems personnel, an incumbent will expand advanced clinical analytics capabilities and relevant components of the data and analytics infrastructure while maintaining high standards of data governance in alignment with industry and regulatory standards. Work requires knowledge of hierarchical and relational database design and application development including but not limited to SQL server, SSIS, VBA, ODBC, AWS. Requires experience in working with Epic EMR data sets in Clarity and Caboodle. Also requires familiarity with EMR reporting and business intelligence tools and expertise with respect to data architecture, technical documentation and end-user training/support. Key Responsibilities Include: Direct querying aqainst the Epic EMR data sets in Clarity and Caboodle (This requires Epic certification) Facilitates data-influenced decision making across VMFH; creates actionable insights from data to assist all levels of management and clinical leadership in making key business and clinical quality decisions. Strives to become a recognized internal subject matter expert and consultant on clinical, quality, data governance and population health data and data sources. Develops, validates, applies and maintains scalable data models including visualizations, statistical models and predictive/prescriptive (machine learning) models. Continuously reviews and updates deliverables to align with current regulatory, contracted and evidence-based quality metrics; researches and applies industry best practices in clinical population health analytics and data management. Works directly with clinicians and business intelligence staff to assure the integrity of clinical data used for analytics and reporting, including supporting initiatives to define and validate new clinical data mart tables. Builds competencies, under the direction and mentorship of higher-level colleagues, in advanced predictive analytics methods and data consolidation. Consults with stakeholders to discuss/understand business needs/requirements and to identify viable technological solutions/opportunities; prepares detailed specifications/record layouts and/or current/revised work flow diagrams from which interfaces/applications/databases will be written. Designs, develops (including complex coding) and documents interfaces/applications/databases that address user needs and meet professional development standards; develops scenarios and scripts to test new/updated tools to ensure desired functionality and that results produced are in line with objectives; troubleshoots/debugs problematic performance/issues; transfers programs to production environment when testing has been completed successfully; prepares and conducts end-user training as necessary. Maintains/updates interfaces/applications/databases once implemented; makes changes in tables/logic and tools; adds and deletes codes and other information; works with IT staff and other resources when systems are being upgraded to identify impact on existing interfaces. Serves as point-person for all issues and/or malfunctions involving the technical aspects of the assigned programs/tools; receives general alerts in the event of a problem, runs internal diagnostics to identify problems, troubleshoots and identifies causes/issues and executes timely resolution that may involve reconfiguration or re-programming of internal code. Provides internal consulting for departments in overall data management concepts/tools and select special applications to facilitate automation of end-user processes and workflows. Performs necessary procedures to ensure the safety of information systems assets and to protect systems from intentional or inadvertent access or destruction; implements security procedures to accommodate system and user requirements. Job Requirements - Bachelor's degree of Science in a Quantitative Discipline (BS in mathematics, statistics, health services research, informatics, epidemiology or research-oriented MPH) and three years of related work experience in quantitative data analysis, including one year in healthcare context. - Or any equivalent combination of education and experience which provides the required knowledge, skills and abilities to perform the essential functions of the position. - EPIC Certification (EPIC) required.