Hello and thank you for your interest! We're looking for folks nationwide who are great at data entry and typing. We offer a flexible work from home remote position that allows you to stay home with the family! The pay range is flexible from $16/ph to $30/ph DOE and level of experience. You'll meet these requirements to work from home remotely • Stable Internet connection • Work can be done using the following: Phone device, laptap or computer • Must be able to type accurately with a minimum speed of 30 words per minute • Able to focus on tasks without being distracted • Must be resident of the US • Not afraid of emailing clients as needed We're looking for folks who we can depend on who can work from home remotely without distraction and are go-getters. Pay range from 16 to 30 hourly depending on the role, level of experience and proven ability to work from home at the same level as from an office. Data entry clerks come from all different backgrounds including, data entry, telemarketing, customer service, sales, clerical, secretary, administrative assistant, warehouse, inventory, receptionist, call center, part-time, retail fields & more • Must be 16 years of age or older • Must be proficient with basic PC skills • Must have an internet connection • Basic english written language • Basic english spoken language Thank you for your interest!

CDC ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development As a CDC I at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You will take responsibility for clinical research deliverables, applying your skills to ensure quality and efficiency. Key responsibilities include: * Performs data review of clinical trial data, including query management * Performs reconciliation review of external data against EDC data * May assist in creating study documents or assist in running study reports and metrics * Performs additional review activities for interim and final database locks as needed. * Files study documentation in electronic Trial Master File (eTMF) and department project files. * Performs periodic quality review of eTMF documents. * Assists with taking meeting minutes and documenting/tracking study data management activities. * Performs data archival activities. * Performs inspection readiness activities and supports CDM team during internal and regulatory inspections * May support the set-up and testing of study data collection tools. Additional Activities * Assists with quality review of above activities performed by the CRO, as needed. * Ensure compliance with own Learning Curricula, corporate and/or GXP requirements. * Performs other duties as assigned. Your Profile: You will bring relevant clinical research experience, along with the following qualifications and skills. * Ideally 1 or more years relevant work experience, or equivalent combination of training and experience. * Familiar with electronic data collection systems (EDC) * Preferred knowledge of data management best practices & technologies as applied to clinical trials. * Preferred knowledge of FDA and ICH regulations and industry standards applicable to data capture and data management process. * Strong attention to detail, and organizational skills * Good time management skills * Quick learner and comfortable learning new technologies and systems * Good knowledge of office software (Microsoft Office). #LI-JC3 What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: - Various annual leave entitlements - A range of health insurance offerings to suit you and your family’s needs. - Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. - Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. - Life assurance - Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Wondering what’s within Beckman Coulter Diagnostics? Take a closer look. At first glance, you’ll see that for more than 90 years we’ve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We’re building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you’ll see we are invested in you—providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful. Beckman Coulter Diagnostics is proud to work alongside a community of fellow Diagnostics Companies at Danaher. Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges. The Material Safety Data Sheet (MSDS) Author for Beckman Coulter Diagnostics is responsible for ensuring that Beckman Coulter products, processes, and documentation comply with local, national, and international chemical safety and regulatory requirements, enabling safe product use and global market access. This position is part of the Global Chemical Compliance Department and will be fully remote. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Global Chemical Compliance team and report to the Director of Global Compliance and Regulatory Affairs, responsible for global chemical compliance strategy and regulatory alignment. If you thrive in a highly collaborative, global-facing role and want to help build a world‑class compliance organization—read on. In this role, you will have the opportunity to: - Generate and maintain Safety Data Sheets (SDSs) in compliance with worldwide chemical user safety regulations. - Partner cross‑functionally with product developers, chemists, and site teams to support chemical compliance across Beckman Coulter locations. - Interpret and apply evolving global chemical regulations to products, processes, and documentation. - Develop and support chemical compliance strategies, including risk identification, mitigation planning, and regulatory readiness. - Provide guidance and subject‑matter expertise to internal teams on safe handling, labeling, and disposal requirements. - Support audits, regulatory inquiries, and internal compliance initiatives as required. The essential requirements of the job include: - Bachelor’s degree in Chemistry, Chemical Engineering, Environmental Science, Toxicology, or a related field. - 5+ years of professional experience in chemical compliance, regulatory affairs, or a related discipline. - Demonstrated knowledge of global chemical safety regulations governing the creation and management of SDSs. - Experience working cross‑functionally with technical and scientific stakeholders. - Ability to travel periodically to the United States (minimum once per year). It would be a plus if you also possess previous experience in: - UL WERCS - Oracle Business Systems - Prior experience supporting in‑vitro diagnostic devices or other highly regulated industries At Beckman Coulter Diagnostics we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Diagnostics can provide. Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com.

• Lead, manage, and develop a team of data engineers, fostering a culture of technical excellence, independence, collaboration, and accountability. • Create and execute a Data Engineering roadmap that helps ReUp to achieve its goals. • Partner with technology, analytics, finance, B2B, and B2C teams to define data requirements, and design and develop solutions that drive value for ReUp’s clients and learners. • Oversee the design, development, testing, implementation, maintenance, and continuous improvement of data pipelines and warehouses that ingest, transform, store, and provide access to student and institutional data to power business intelligence products, ML models, cloud-based web applications, and marketing and coaching services. • Champion automation, observability, and performance to ensure ReUp’s pipeline efficiently and reliably delivers quality data to end users. • Proactively identify, triage, and resolve data quality and availability issues through root-cause analysis, remediation, monitoring, and cross-functional collaboration. • Define and monitor SLAs for data quality, workflow status and runtime, incident response and resolution time, and team velocity. • Define and implement data engineering standards and best practices. • Support data security, compliance, and governance initiatives.