Role Description Texas Oncology is looking for a Data Coordinator to join our team! This position will support the Dallas Sammons location and is a Remote position. Typical hours are Mon-Fri from 8am-5pm. This position can be either a level 1, 2 or Sr based on experience. The Data Coordinator is responsible for the collection, coordination, processing, and quality control of clinical trial data, maintaining research protocol and other research files as applicable. Works with clinical staff to meet data entry timelines and communicate any concerns about the data. Works in compliance with US Oncology Research (USOR) Standard Operating Procedure (SOP), principles of Good Clinical Practice (GCP), and all applicable federal, state, and local regulations. Supports and adheres to the US Oncology Compliance Program to include the Code of Ethics and Business Standards. Responsibilities - Extrapolate data from source records into case report forms for all patient visits and ensure timely data submission in accordance with USOR SOPs. - Responsible for resolving queries, communicating concerns or questions about data to clinical staff and/or research management. - Utilizes USOR clinical trial management system to access research forms and keep current all applicable patient reporting and tracking functions including but not limited to subject CRF Binders/Folders. - Maintains research records in a confidential manner according to practice policies, sponsor confidentiality agreements, HIPAA guidelines, and any other applicable regulations. - Actively participates in sponsor monitoring and auditing visits, ensuring that all data and queries are entered and resolved in accordance with USOR and sponsor requirements. - Assist with ordering and maintaining research supplies. - Assist with scheduling patient follow-up appointments and/or procedures required to maintain protocol compliance. - Assist with collecting and processing of specimens, imaging documents, and other items required for research purposes. Qualifications - Level 1: High School Diploma required; Associates Degree strongly desired; Bachelor's Degree preferred. - 0-3 Years work experience; Some medical office experience required; preferably oncology. - Level 2 (in addition to level 1 requirements): Minimum 3 years medical office experience (preferably oncology); Minimum 3 years as Data Coordinator required; SoCRA or ACRP cert. preferred. - Level Sr (in addition to level 1 and 2 requirements): Medical terminology required; Minimum 7 years as a Data Coordinator required. - Business Experience: Experience in Microsoft Office; Experience with computer data entry and database management; Experience in clinical research desired; High computer literacy required. - Specialized Knowledge/Skills: Excellent written and oral communication skills; Excellent multi-tasking skills; High attention to detail and accuracy; Ability to independently organize, prioritize, and make decisions; Knowledgeable of medical terminology. Working Conditions - Environment: Traditional office environment. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations, and other conditions common to an oncology/hematology clinic environment. - Physical Requirements: Large percent of time performing computer-based work is required. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range. Benefits - Competitive benefits package including Medical, Dental, Vision, Life Insurance. - Short-term and Long-term disability coverage. - A generous PTO program. - A 401k plan that comes with a company match. - A Wellness program that rewards you for practicing a healthy lifestyle. - Tuition Reimbursement. - An Employee Assistance program. - Discounts on some of your favorite retailers.

Role Description We are seeking a Sr. Data Analyst who will be responsible for developing, implementing, and managing a plan to translate data into insights. The Sr. Data Analyst will provide expertise in data analysis and illustrations to articulate and monitor programs, projects, and general business success. The Sr. Data Analyst will serve as a data consultant to the assigned area and to provide complex analysis and reporting on various outcomes. The BESAFE (Building Education and Skills to Address Substandard and Falsified Medicines) Initiative at the Johns Hopkins Bloomberg School of Public Health seeks a Sr. Data Analyst to support a growing portfolio of primary research, policy translation, and global partnership activities focused on substandard, falsified, and counterfeit (SFC) medical products. Reporting to the Senior Program Officer, this position plays a central role in managing, analyzing, and communicating evidence generated across BESAFE's research workstreams. - Align assessment strategy with strategic objectives and goals. - Translate data into insights to be used to support positive and enhanced outcomes. - Collaborate with leadership to plan and implement assessment activities, including consultation on data collection, data analysis, reporting of assessment outcomes, and using results to improve programs and services. - Prepare an annual assessment report to summarize findings across the school/division. - Lead the design of clean, impactful, user-friendly data visualizations supporting strategic goals. - Communicate findings compellingly and visually through dashboards, reports, briefing decks, stories, scorecards, executive briefings, etc. for different audiences using software like Power BI and Tableau. - Provide insights on data patterns and trends, make strategic recommendations from analysis. - Design and build data visualizations from concept to data analysis to the final step of visualization, informed by principles of good data storytelling. - Collect and analyze various complex data and information; in collaboration with others, perform statistical analysis and summarize findings in applicable reports or other communication mediums. - Use data visualization techniques to distill and clarify complex processes or data sets. - Conduct quality assurance and review of all data visualizations to ensure accuracy, usability, and adherence to existing branding and style guidelines. - Create and maintain a library or repository of analysis documents, slides, and links to dashboards. - Work with leadership to develop an efficient system for planning and administering surveys to minimize survey fatigue and maximize the collection of actionable data. - Other duties as assigned. In Addition to the Duties Listed Above: - Oversee the full data lifecycle for BESAFE studies: from instrument development and database architecture through data cleaning, analysis, and visualization. - Contribute directly to BESAFE's mission of converting research evidence into actionable clinical and regulatory guidance. - Support cross-country research coordination across BESAFE's active geographies — including the United States, Nigeria, Senegal, South Africa, Kenya, and Rwanda. - Multi-Country Survey Data Architecture: Build and maintain database infrastructure for the six-country HCP KAP survey. - Traditional and Non-Traditional Publication Support: Contribute to the full publication pipeline across peer-reviewed journals, policy white papers, conference reports, and media-facing science communication products. - Policy-Facing Evidence Translation: Repackage findings from systematic reviews and primary studies into data assets for regulatory bodies, clinical associations, and donors. - Qualitative Data Management: Manage MAXQDA codebooks, audit trails, and intercoder reliability calculations across BESAFE qualitative studies. - CME Data Pipeline: Analyze learner outcome and pre/post assessment data from BESAFE's ACCME-accredited JHU CloudCME course. Qualifications - Bachelor's Degree. - Five years of related experience. - Additional education may substitute for required experience, to the extent permitted by the JHU equivalency formula. Requirements - Experience in R (ggplot2, R Markdown/Quarto). - Advanced knowledge of analysis software such as Power BI, Tableau, Excel. - Understanding of relational and dimensional data models and structures. - Experience working with querying tools such as SQL, Python, R Data. Benefits - Starting Salary Range: $62,900 - $110,100 Annually (Commensurate w/exp.) - Employee group: Full Time - Schedule: Monday to Friday: 9:00am – 5:00pm - FLSA Status: Exempt - Location: Remote - Department name: Popltn Fmly and Reproductive Hlth Srvs - Personnel area: School of Public Health

Role Description AECOM is seeking Data Center Quality Assurance Inspectors nationally. This position can be remote. - Inspect building systems, including mechanical and electrical, for compliance with contract requirements and industry standards. - Review contractor shop drawings and submittals to confirm alignment with project specifications. - Monitor the installation, testing, and commissioning of electrical and mechanical systems, confirming proper functionality and performance. - Identify and report non-conformances, coordinating with contractors and engineers to implement corrective actions. - Maintain detailed inspection reports, logs, and records for quality control and compliance tracking. - Oversee corrective actions for unacceptable construction work and support final inspections, punch lists, and project closeouts. - witness and document critical tests, such as pressure tests, leak tests, and system start-ups. - Verify the quality of materials, workmanship, and equipment installations to confirm adherence to project specifications. - Work closely with contractors, engineers, and other inspectors to resolve issues. - Maintain professionalism in attire and communication during all time on site and in meetings. - Represent the Client in alignment with contract requirements and project deliverables. - Coordinate client Outage / Shutdown Procedure. - Coordinate GC Workplan and advise if the construction contractor fails to promptly remove, correct, or replace unacceptable construction work, and assess any delays caused by such failure. Qualifications - Minimum Requirements: BA/BS + four years of relevant experience or demonstrated equivalency of experience and/or education. - Preferred Requirements: 7 years of experience with construction and/or quality management. - CQM or other professional certifications. - Bachelor’s degree in construction management, engineering, or architecture. Requirements - Sponsorship for US employment authorization is not available now or in the future for this position. - Relocation is not available for this position. - Potential up to 90% travel anywhere in US. - All newly hired employees are required to attend an in-person Day 1 onboarding at an AECOM office location as a condition of employment. Benefits - Medical, dental, vision, life, AD&D, disability benefits. - Paid time off, leaves of absence, voluntary benefits. - Perks, flexible work options, well-being resources. - Employee assistance program, business travel insurance. - Service recognition awards, retirement savings plan. - Employee stock purchase plan.

• Reviews architectural prints and technical drawings to identify required data points (dimensions, room areas, quantities, notes, and callouts). • Enters extracted data into Excel workbooks and standardized templates with accuracy and consistency. • Ensures data is captured using the correct units of measure and required formatting standards. • Performs routine validation and self-audits to confirm entries match source documents. • Identifies discrepancies, missing information, or conflicting details and escalates for resolution. • Maintains organized documentation and version control for spreadsheets and supporting files. • Communicates status updates and completion tracking to the reporting manager as requested. • Maintains confidentiality and follows company data handling and documentation requirements.