Title: Professor, Clinical Faculty Appoint (CFA) - Musculoskeletal Imaging Location: Houston United States Job Description: The University of Texas MD Anderson Cancer Center is a world-renowned center for oncological care and research. The Department of Musculoskeletal Imaging, Division of Diagnostic Imaging at MD Anderson Cancer Center invites applications for a full-time, open rank clinical faculty appointment. The department prides itself on its balanced work-life and collegial culture. The Musculoskeletal Imaging Department consists of 11 musculoskeletal radiologists who provide diagnostic imaging services to diagnose, stage, and follow-up patients with known or suspected malignancy using conventional radiographs, computed tomography (CT), magnetic resonance imaging (MRI) and positron emission tomography (PET). Members of the department are responsible for the following: - Delivering excellent, comprehensive, and compassionate care for patients; - Providing multimodality approaches to musculoskeletal imaging including CT, MRI, whole body MRI, PET, and conventional radiography; - Educating medical students, residents, and fellows; - Developing academic and scholarly programs and projects; and - Fostering interdisciplinary and collaborative approaches to clinical care, research, and education. This position consists of a target base salary, various incentive/bonus compensation, and retirement benefits placing our remuneration package well in the 75th percentile nationally. Comprehensive health, wellness, time off, and various savings benefits are also included. The University of Texas MD Anderson Cancer Center offers excellent benefits, including medical, dental, paid time off, retirement, tuition benefits, educational opportunities, and individual and team recognition. This position may be responsible for maintaining the security and integrity of critical infrastructure, as defined in Section 113.001(2) of the Texas Business and Commerce Code and therefore may require routine reviews and screening. The ability to satisfy and maintain all requirements necessary to ensure the continued security and integrity of such infrastructure is a condition of hire and continued employment. It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunity without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, disability, protected veteran status, genetic information, or any other basis protected by institutional policy or by federal, state, or local laws unless such distinction is required by law. Additional Information - Requisition ID: 180134 - Employee Status: Regular - Minimum Salary: US Dollar (USD) 0 - Midpoint Salary: US Dollar (USD) 0 - Maximum Salary : US Dollar (USD) 0 - FLSA: exempt and not eligible for overtime pay - Work Location: Hybrid Onsite/Remote

The Statistical and Data Management Center of the Hepatitis B and HIV Cure Consortium (BICC) is seeking a Sr. Biostatistician who will be responsible for data management and statistical analysis for a multinational cohort representing the global diversity of people living with HIV and chronic Hepatitis B. The Sr. Biostatistician is responsible for data management and analysis of multicenter clinical trials. The Sr. Biostatistician will supervise research data analysts and work with principal investigators to analyze and manage data from studies. Specific Duties & Responsibilities - Work with a multidisciplinary group on clinical trials and other longitudinal studies. - Collaborate with investigators on research projects with primary responsibility for analysis and presentation of project data. - Provide integration and analysis of biodata from multiple sources. - Provide expertise in statistical design, data management, and data analysis. - Contribute to the development and application of statistical methods to advance scientific goals of various projects. - Serve as lead Biostatistician with investigators to develop objectives, design sampling, randomization, and statistical analysis plans to achieve study objectives. - Design and perform appropriate methodologic procedures for statistical analysis, overall descriptive statistics, exploratory data analyses, including graphs, schematic summaries, and necessary transformations and confirmatory data analyses, including statistical tests and/or modeling. - Design, implement, and manage computerized systems for analysis of complex research projects to prepare scientific presentations related to study results. - Perform sample size and power calculations, generate randomization schema, and prepare statistical sections for research protocols and manuscripts. - Participate in regularly scheduled meetings with investigators and team that require statistical input. - Design tables and statistical procedures for specific research studies. - Write statistical design, methods, and analysis for manuscripts and research proposals. - Analyze data and prepare tables for interim and final reports. - Develop and apply new statistical methodologies. - Ensure data integrity and compliance with security policies governed by HIPAA and the Johns Hopkins IRB. - Oversight of one or more professional team members and project milestones. - Prepare progress reports and present to leadership. - Other duties as assigned. Minimum Qualifications - Master's Degree in Biostatistics, Epidemiology, or related quantitative field. - Three years of related experience. - Additional education may substitute for required experience, and additional related experience may substitute for required education beyond a high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula. Technical Skills & Expected Level of Proficiency - Analytic Methodological Development - Intermediate - Clinical Trial Design & Data Management - Intermediate - Data Integration - Intermediate - Interpersonal Skills General - Intermediate - Project Management - Intermediate - Regulatory Compliance - Intermediate - Scientific Communication - Intermediate - Statistical Methods - Intermediate - Statistical Programming - Intermediate The core technical skills listed are most essential; additional technical skills may be required based on specific division or department needs. Classified Title: Sr. Biostatistician Role/Level/Range: ACRP/04/ME Starting Salary Range: $64,600 - $113,300 Annually (Commensurate w/exp.) Employee group: Full Time Schedule: Monday to Friday: 8:30am – 5:00pm FLSA Status: Exempt Location: Remote Department name: Epidemiology Personnel area: School of Public Health

Summary: The Clinical Genomics Scientist I analyzes clinical genetics data, curates variants and genes, and summarizes findings for clinical reports. Our scientists assist laboratory directors and R&D with validation of cutting-edge technologies and software platforms. The Clinical Genomics Scientist I position is a remote work opportunity, with daily huddles, clear objectives, and flexible scheduling. Come join our team from the comfort of your home office! Duties and Responsibilities: - Curation (50%): curation of variants, genes, and gene-disease correlation following ACMG guidelines - Analysis (30%): analyzing clinical genomics data, selecting variants for curation/confirmation, variant nomenclature following HGVS guidelines - Other (20%): may involve clinical report drafting, test validation, process refinement, presenting findings, monitoring test turnaround time and task delegation Qualifications/Experience - Degree: PhD or MD in clinical medicine, genetics, molecular biology, or equivalent. Or strong candidates with a Master’s degree and relevant experience. Desired: MB(ASCP) certification. - Familiarity with American College of Medical Genetics (ACMG) variant curation guidelines. - Knowledge of genomic variation and its correlation with human disease. - Expertise in concepts of clinical medicine, genetics, genomics, or molecular biology. - Experience in data quality assessment and communicating genetic details effectively. - Excellence in reading/writing medical language. - Proficiency in Microsoft Office (Excel, Word, PowerPoint, Outlook). - Desired: experience in bioinformatics analysis, variant effect prediction algorithms, and scripting languages Competencies: Quality Assurance, Analytical, Problem Solving, Technical Skills, Interpersonal Skills, Oral and Written Communication, Teamwork, Organizational Support, Safety and Security, Dependability, Innovation, Adaptability. Physical Demands and Work Environment: - At your Home Office: - Frequently required to sit, using screen, keyboard, and mouse. - Punctuality attending virtual meetings - Occasional weekend rotation may be needed (for example, once a month)

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche. The Clinical Development Lead, Oncology/Pathology is responsible for planning and implementation of Clinical Development activities for novel medical value diagnostic solutions in the areas of oncology and tissue-based pathology at Roche Diagnostic Solutions (RDS), with a primary focus on Companion diagnostic/Personalized Healthcare solutions. The Opportunity: - Designs scientifically sound clinical studies and study programs in cross-functional teams - Makes substantial contributions to the Clinical Development strategy for the relevant therapeutic/disease area(s) - Leads clinical study design and execution, including critical review of study results, protocol and report generation to support new product development - Works with colleagues from Clinical Operations, Regulatory Affairs, Biometrics, Development, Quality, Business, and other functions to ensure appropriate implementation of clinical development strategies - Leads medical/scientific input and preparation of regulatory submissions as well as responses to reviewers from regulatory agencies - May participate in external interactions with health authorities (HAs) - Maintains clinical, regulatory, and scientific expertise as it relates to IVD product development and regulatory documentation - Builds and maintains close relationships with external thought leaders, supports preparation of advisory boards within the assigned indication area - Builds and maintains strong, collaborative relationships with cross-functional leaders, key internal and external stakeholders and other alliance partners, in meeting business goals and ensuring operational excellence - Drives competitive differentiation, innovation and early pipeline activities and develops intellectual property strategy - Develops and manages external development partnerships (industry and academia) - Leads comprehensive literature reviews, supervises collation of relevant clinical and scientific information from different sources, and creates new scientific content (without guidance/direction) - Solves or leads others to solve complex outcomes; uses sophisticated analytical thought to - exercise judgment and identify innovative solutions - Acts as a coach for colleagues with less experience and helps them develop skills/expertise - Permanently optimizes processes to increase quality and efficiency standards - Drive patient and customer-centricity (mindset, behaviors and actions) by always putting the needs of patients and the customers first - Partner across diverse regions, cultures, and time zones to create an environment of belonging, inclusion and diversity - Working across Medical Affairs and Clinical Operations communities to identify mutual value and opportunities for collaboration - Demonstrate flexibility and adaptability to perform in a fast-paced, matrixed environment where fluid, cross-team collaboration is crucial - Model Roche’s values of integrity, courage, and passion (culture, mindset and behaviors) Who You Are - You have a medical degree or advanced degree (PhD, PharmD or equivalent) in Life Sciences, Oncology, Immunology, Molecular Biology and or Anatomic Pathology - You have 7+ years academic, diagnostics or pharma industry experience, - You have familiarity with global regulatory bodies (FDA, EMA, PMDA) - You have good knowledge in applicable standards and regulations (ICH-GCP, IVDD/IVDR, MDR, FDA, NMPA regulations etc.) and understanding of the healthcare industry or equivalent academic experience - You have in-depth knowledge of the multidisciplinary functions involved in a company’s drug development process, e.g., clinical operations, biostatistics, regulatory, commercial, etc. and can proactively integrate multiple perspectives into the clinical development process and strategy for best end-results - You have the ability to work with pharmaceutical partners to align the development of a diagnostic test with the development of a specific cancer drug - You have the ability to travel required up to 10% (can vary per project phase and position) - You have the ability to work independently The primary location for this position is Tucson, Arizona, USA (preferred). We will consider US remote candidates. Relocation benefits aren't offered for this position The expected salary range for this position is based on the primary location Tucson, AZ is 120,500-223,700. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.