Ecolab is looking for a Junior Project Coordinator to support process improvement initiatives across the organization. The role will assist the Enterprise Excellence team in applying tools and methodologies aimed at enhancing customer satisfaction and operational efficiency. The position is 1 year fixed-term contract and could be based anywhere in Europe How you'll make an impact: - Assist in the execution of process improvement projects aligned with business goals. - Apply Enterprise Excellence tools and methodologies to identify optimization opportunities. - Support the coordination of multiple projects, helping organize activities and resources. - Foster collaboration across teams to ensure engagement and alignment. - Prepare progress reports and share outcomes with the relevant stakeholders. Qualifications: - Bachelor’s degree (preferably in business, engineering, or related fields). - 1–3 years of experience in project support or continuous improvement roles. - Interest in process improvement methodologies (e.g., Lean, Six Sigma). - Strong organizational, communication, and teamwork skills. What’s in it for You: - The opportunity to contribute to impactful improvement projects that deliver value to our customers. - A learning experience within a company committed to excellence and innovation. - The support of a collaborative team that values diverse perspectives and fresh ideas. About Ecolab: At Ecolab, we prioritize our talent-first philosophy by creating the most capable and diverse team to excel at our nearly three million customer sites. Building on a century of innovation, our 48,000 associates help deliver comprehensive science-based solutions, data-driven insights and world-class service to advance food safety, maintain clean and safe environments, and optimize water and energy use, and improve operational efficiencies and sustainability for customers in the food, healthcare, life sciences, hospitality and industrial markets in more than 170 countries around the world. Our solutions not only enhance operational efficiency but also contribute to sustainability and public health, making a positive impact on the world. We are committed to eliminating unnecessary complexities and embracing a beginner's mindset, continuously seeking new perspectives and innovative solutions to stay ahead in a rapidly changing world. Ecolab’s commitment to diversity, equity and inclusion (DE&I) reflects our longstanding value of working together to integrate diverse perspectives to challenge ourselves, reach our goals and do what’s right. Apply today and join one of the most ethical companies with over a hundred years of history. Join Ecolab and help us protect what’s vital. #li-eu

Senior Project Manager - Internal Medicine 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 Senior Project Manager at ICON, you will be responsible for leading and manage projects, ensuring successful execution and delivery of project objectives. What You Will Do: You will manage day-to-day project and programme management activities, supporting your team to deliver quality outcomes. Key responsibilities include: - Developing and executing project plans, focusing on achieving project goals and objectives. - Leading cross-functional teams to ensure the successful implementation of project activities. - Collaborating with stakeholders to identify project requirements and define project scope. - Mentoring and guiding team members, fostering a culture of excellence and continuous improvement. - Driving the development of project documentation and reports to present findings to stakeholders in a clear and actionable manner. - Staying abreast of industry trends and emerging technologies to integrate best practices into project management strategies. - Contributing to organizational growth through effective project leadership and strategic planning. Your Profile: You will have solid project and programme management experience, with the ability to manage competing priorities and develop your team. Required qualifications and experience: - Bachelor's degree in a relevant scientific discipline or healthcare-related field - Extensive experience in project management, with a proven track record of leading successful projects in the pharmaceutical or biotech industry. - Strong proficiency in project management tools and methodologies, with excellent attention to detail. - Excellent analytical and problem-solving skills, with the ability to develop effective project strategies. - Demonstrated leadership skills, with experience in managing and mentoring teams effectively. - Exceptional communication skills, with the ability to convey technical concepts to diverse audiences. - Detail-oriented, with strong organizational skills to manage multiple projects and deadlines in a dynamic environment. - Willingness to travel as required (approximately 25%) 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

Clinical Trial Assistant - Hamburg 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 Senior Clinical Trial Associate at ICON Plc, you will support the management and execution of clinical trials by handling a range of administrative and operational tasks. What You Will Do: You will take ownership of clinical trial management deliverables, applying your expertise to complex challenges. Key responsibilities include: - Providing administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records. - Assisting in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements. - Collaborating with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study. - Monitoring and tracking trial progress, including managing site communications and ensuring timely delivery of study materials. - Building and maintaining strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support overall project success. Your Profile: You will have a strong foundation in clinical trial management, with the experience to work independently and guide others. Required qualifications and experience: - Bachelor's degree in a relevant scientific discipline or healthcare-related field - Extensive experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements. - Strong organizational and multitasking skills, with the ability to manage multiple tasks and projects effectively. - Proficiency in clinical trial management systems and relevant software, with a keen eye for detail in documentation and data management. - Excellent communication, interpersonal, and problem-solving skills, with the ability to work collaboratively with diverse teams and stakeholders. - Willingness to travel as required (approximately 10%) 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

As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive. Job Location (Full Address): Remote Work - New York, Albany, New York, United States of America, 12224 Opening: Worker Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 500468 Psych Ambulatory Nursing Work Shift: UR - Day (United States of America) Range: UR URCI 214 H Compensation Range: $37.12 - $50.11 The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations. Responsibilities: GENERAL PURPOSE: Under the direction of leadership, is accountable for provision of competent direct patient care based on established standards. Contributes to unit activities and supports enhancement of the care delivery system at the unit level. Supports peers in the delivery of patient care services and assumes an expanded role which may include charge nurse, preceptor, and committee member responsibilities. 40 hours Primarily Days URMC’s Forensic ACT team, will serve justice-involved adults with serious mental illness in Monroe County. The Project FACT team nurse provides overview of physical and behavioral health issues of individuals receiving services from the team. The nurse provides leadership and guidance to the team in addressing all preventative, ongoing and critical health matters. The nurse also coordinates pharmacological services along with the team’s prescriber(s). Nurses are core members of the team and contribute to all clinical decisions in team, including treatment plans and documentation. Rotating on call responsibilities. A university car is provided for use in seeing clients. NYS RN license in good standing. Must possess a valid New York State Driver's license and a satisfactory driving record. Minimum 3 years of Psychiatric experience required, outpatient experience preferred. The University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture to advance the University’s Mission to Learn, Discover, Heal, Create – and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion, creed, sex, sexual orientation, citizenship status, or any other characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law.