Role Description Lead Data scientists at Thoughtworks are responsible for leading and executing data science projects. They employ their profound expertise in statistics, modeling, machine learning algorithms, and data mining methodologies. They integrate this expertise with a comprehensive understanding of related domains to render business value and illuminate data-driven insights, facilitating clear and effective decision-making processes. Their responsibilities encompass: - Devising strategies, executing plans, and operationalizing solutions. - Articulating tangible business outcomes achieved. - Collaborating with cross-functional teams and conveying discoveries to both technical and non-technical stakeholders. - Staying up-to-date with industry advancements, ensuring data quality and security. - Providing guidance to junior team members. As a data scientist at Thoughtworks, you'll work on a range of projects and leverage deep technical knowledge to solve complex business problems. Qualifications - Experience in leading the analysis and modeling of different datasets and overseeing the inception to deploying and productionizing the models. - Experience with statistical modeling, hypothesis testing, machine learning, deep learning, optimization, and other data science techniques to implement end-to-end data science projects. - Understanding of specialized areas of AI with a specialty in at least one (e.g., NLP, computer vision, Generative AI). - Experience with R, Python, or equivalent statistical/data analysis tools, capable of writing production-ready code that is easy to evolve and test. - Ability to gather and preprocess large volumes of structured and unstructured data from various sources, ensuring data quality and integrity. - Experience analyzing datasets using statistical and visualization techniques to identify patterns, trends, and relationships. - Development and implementation of machine learning models, algorithms, and predictive analytics to solve specific business problems or improve existing processes. - Evaluation of model performance using appropriate metrics and validation of models to ensure robustness and reliability. - Ability to interpret and effectively communicate findings and insights to non-technical stakeholders through reports, presentations, and visualizations. - Ensuring compliance with data privacy regulations and ethical standards when handling sensitive information. Requirements - Understanding the importance of stakeholder management and ability to liaise between clients and other key stakeholders throughout projects. - Resilience in ambiguous situations and adaptability in approaching challenges from multiple perspectives. - Willingness to take on risks or conflicts and skillfully manage them. - Eagerness to coach, mentor, and motivate others, aspiring to influence teammates positively. - Proven leadership with a track record of encouraging teammates in their professional development and relationships. - Natural ability to cultivate strong partnerships and understand the importance of relationship building. Benefits - Support for career development through interactive tools and numerous development programs. - Empowerment in career journeys with a focus on helping each other grow.

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