• Writes, reviews, tests, and maintains code to support analytic dataset development and statistical analyses, ensuring accuracy, efficiency, and reproducibility. • Implements data quality initiatives under the guidance of the Registry Lead to ensure accuracy, completeness, and reliability of datasets. • Works closely with the Registry Lead to ensure timely completion of deliverables and adherence to project deadlines. • Assists the Registry Lead in maintaining existing reports and developing new reports as needed. • Produces monthly analytic data cuts, monthly reports, and quarterly reports, ensuring accuracy, consistency, and alignment with reporting requirements. • Serves as an additional point of contact for assigned registries, proactively supporting colleagues by addressing registry-related questions on data structures, outputs, etc. • Provides support on ad hoc projects and analyses as needed. • Creates data pipelines for ingestion of external data sources and integration with clinical registry data to create combined datasets. • Compiles, analyzes and reports statistical data for various projects. • Carries out complex statistical analyses with supervision according to a statistical analysis plan. • Assists Biostatistical Team Lead in the development of new statistical methodology for measurement and analysis of data. • Assesses relevant literature as well as existing data, evaluates the quality of data used in reports and assists with preparation and distribution of periodic reports. • Prepares written reports and summarizes data for investigators with minimal supervision. • Makes original contributions to research projects, takes initiative in professional activities and beginning to be more independent in their statistical decision making. • Closely collaborates and participates in knowledge sharing with other statistical analysts.

Role Description Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. The Clinical Science Liaison will have responsibility for clinical and academic collaborations within the Clinical Science and Collaborations segment of the Ultrasound Organization. Research is focused upon driving evidence generation from collaborations, clinical trials, and enhancing partnerships with external key thought leaders and luminaries. This is a role well suited to an ambitious professional, looking for the next step in their career. As a Clinical Science Liaison, you will be responsible for: - Scientific expertise for developing research collaborations. - Remain current with published literature and clinical results for strategic purposes. - Promote continuous dialogue with collaborators to identify opportunities for collaboration on research topics and to translate these into project proposals. - Provide scientific feedback and advice to internal and external partners regarding our technologies. - Work directly with collaboration partners and research staff at luminary academic institutes. - Compile data and write project results, while performing statistical analysis and using statistics to develop study endpoints, sample size, etc. - Provide oversight of investigator-initiated research studies. Collaboration Management: - Contribute to study development and start-up process including reviewing protocols, drafting of IRB packages, consent forms, designing and/or reviewing CRFs, writing collaboration contracts, executing collaboration contracts, preparing volunteer Informed Consent forms, developing study documents, organizing, and presenting at investigator meetings, while working with management on monitoring strategy. - Negotiating and finalizing contracts for execution with support from legal, regulatory and compliance. - Ensure that all study related documents are tracked, filed and reviewed, and complete according to SOPs, regulatory requirements and protocol. - Administrative and logistical tasks, including tracking, collecting, distributing, and filing study documentation. - Ensure collaborations are on track for site initiation, subject recruitment and enrollment, as well as close-out. - Clinical trial execution and monitoring. - Work with management team to define timelines of milestones, deliverables and data. - Design reports and metrics that are useful management tools for projects. - Adapt to collaboration archiving tools and work with cross-functional teams and tools to ensure payment of milestones and deliverables. - Monitor activities at clinical study sites to ensure adherence to GCP, ICH, SOPs, FDA guidelines, study protocols, and internal collaboration controls including compliance. Qualifications - Ph.D. or other doctorate degree in Cardiology, Imaging, epidemiology or related disciplines +3 years of relevant experience; master’s degree. - Expertise in Imaging. - Expertise in imaging, cardiology, radiology, procedures. - 5+ years of experience in working with clinical research experience in med tech industry, health care or pharmaceutical. - At least 4+ years of clinical monitoring experience or clinical trial experience. - Experience in working with clinical and academic research environments. - In-depth knowledge of clinical trials and the critical elements for success in clinical trials. - Knowledge of medical terminology, as well as knowledge of clinical research and scientific principles. Benefits - Medical insurance. - Dental insurance. - Vision insurance. - 401(k) retirement plan. - Life insurance. - Long-term and short-term disability insurance. - Paid parking/public transportation. - Paid time off. - Paid sick and safe time.

Role Description At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. You will act as a strategic clinical advisor, partnering with internal Solventum teams and key customers to drive best practices and deliver advanced education. You will lead priority customer engagements, provide escalated clinical and technical consultation, and support economic value discussions with evidence-based data. As a Peri-op Area Clinical Leader, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by: - Acting as strategic advisor to internal Solventum teams on wound care clinical strategy and industry best practices - Collaborating with sales leadership to identify opportunities to educate and upskill teams and individuals on clinical or technical consultative practices - Presenting compelling data and clinical application during priority planned customer engagements - Building and maintaining relationships with key healthcare customers to ensure customer loyalty and satisfaction - Engaging alongside local teams to plan & lead comprehensive customer education events - Directly interacting with customers who require escalated consultation on clinical or technical on-label scenarios - Serving as a consultative partner to various internal business stakeholders on clinical and/or technical matters - Supporting economic objection handling with customers by articulating evidence-based clinical efficacy and the connection to economic value - Aiding in resource management for conversions/evaluations - Maintaining clinical/technical relevance through ongoing continuous learning and participation in professional associations - Understanding and translating current relevant industry standards (e.g., ERAS, AAMI) Qualifications - Bachelor’s Degree or higher AND 2 years of healthcare experience in a hospital, surgery center, or long-term care environment - OR High School Diploma/GED AND 4 years of healthcare experience in a hospital, surgery center, or long-term care environment - Experience with Microsoft Office applications (i.e. Excel, Power Point, Outlook) - Current, valid Driver’s License Requirements - Current certification(s): BSN, RN, CNOR - Strong understanding of clinical value drivers across hospital care areas and alternative sites of care - Excellent organizational and time management skills - Understanding of the principles of adult learning - Demonstrated analytical, problem solving, project management, and implementation skills - Proven ability to cultivate strong internal and external collaborative relationships - Experience with public speaking and technical presentations Benefits - Medical, Dental & Vision - Health Savings Accounts - Health Care & Dependent Care Flexible Spending Accounts - Disability Benefits - Life Insurance - Voluntary Benefits - Paid Absences - Retirement Benefits Company Description Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided by empathy, insight, and clinical intelligence, we collaborate with the best minds in healthcare to address our customers’ toughest challenges.

Role Description As a Clinical Research Associate at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: - Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. - Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. - Collaborating with investigators and site staff to facilitate smooth study conduct. - Performing data review and resolution of queries to maintain high-quality clinical data. - Contributing to the preparation and review of study documentation, including protocols and clinical study reports. Qualifications - Bachelor's degree in a scientific or healthcare-related field. - Minimum of 2 years of experience as a Clinical Research Associate. - In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. - Strong organizational and communication skills, with attention to detail. - Ability to work independently and collaboratively in a fast-paced environment. - Willingness to travel as required (approximately 60%). Benefits - 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.