• Accountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout • Serve as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements • Develop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas • Influence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives • Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including for example, novel site models, community-based research initiatives etc • Capture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct • Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery • Leverage performance metrics to anticipate issues, intervene decisively, and maintain momentum toward clinical milestones • Drive inspection readiness as a continuous discipline across sites • Collaborate across functions and with vendor partners to resolve operational barriers, ensuring delivery with speed and quality • Maintain advanced understanding of local treatment paradigms and standard of care to influence strategic country/site selection and protocol localization • Provide oversight and quality assurance for vendor monitoring, escalating risks proactively • Cultivate a portfolio of strategically aligned, high-impact investigators

Role Description We are currently seeking a Clinical Research Associate (Level II or Senior) to join our diverse and dynamic team. As a CRA II/Senior CRA at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. - 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 health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role. - Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior 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. - Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license. Benefits - Competitive base salary and performance related incentives. - Health and wellbeing programmes including medical, dental, and vision coverage where applicable. - Retirement and pension plans. - Life assurance and disability coverage. - Employee assistance programmes and wellbeing resources. - Learning and development opportunities through structured training and career pathways. - Benefits may vary depending on role and location. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Salary Range $91,336.00-$114,170.00

Role Description As a Vascular Area Clinical Leader at Solventum, 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. Your impact will include: - 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 4 years of healthcare experience in a hospital setting. - OR High School Diploma/GED AND 8 years of healthcare experience in a hospital setting. - Experience with Microsoft Office applications (i.e. Excel, Power Point, Outlook). - Current, valid Driver’s License. Requirements - Current certification(s): BSN, RN, VA-BC, CRNI. - 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 - Competitive pay and benefits. - Medical, Dental & Vision coverage. - Health Savings Accounts. - Health Care & Dependent Care Flexible Spending Accounts. - Disability Benefits. - Life Insurance. - Voluntary Benefits. - Paid Absences. - Retirement Benefits.

Role Description The Supervisor, Clinical Services – Site of Care (SOC) is responsible for providing day-to-day leadership and strategic oversight to the SOC business unit. This role is focused on optimizing operational performance through: - Talent development - Quality improvement - Innovation - Cost reduction The Supervisor plays a key role in guiding the Rep/Tech to ensure high-quality service delivery, regulatory compliance, and seamless coordination across internal departments. Core responsibilities include: - Managing daily operations - Driving performance against established metrics - Overseeing training and policy implementation - Supporting the accurate and timely redirection of patients to appropriate sites of care This position requires strong collaboration with internal stakeholders to ensure that service level expectations for both physicians and patients are consistently met. The Supervisor is also accountable for: - Ensuring standardization of processes - Promoting consistency in workflows - Maintaining compliance with all applicable federal, state, and client-specific requirements - Representing the SOC team in client-facing meetings - Supporting new client implementations - Serving as a primary escalation point for operational issues Qualifications - 2-3 years of experience in a people leadership or supervisory role and/or Subject Matter Expert (SME) or Lead role - Demonstrated ability to work in fast pace, multi-tasking team environment while meeting deadlines - Highly skilled in leading significant change efforts - Ability to summarize complex issues and problems into a concise report, focused on key findings and outcomes - Proficiency in developing communication strategies for a wide array of audiences that support strategic objectives - Proficiency in the management of time, flexibility, and influencing colleagues to meet demanding timelines - Strong coaching and interpersonal skills - Ability to cultivate a strong internal culture designed around collaboration, feedback, motivation and accountability - Strong leadership and collaboration skills that drive results Requirements - 2 plus years working with Novologix and SalesForce - Excellent verbal and written communication skills - Ability to form cross-functional partnerships to accomplish goals - Associates Degree or Bachelor's degree preferred Education - High School Diploma or equivalent GED Benefits - Medical, dental, and vision coverage - Paid time off - Retirement savings options - Wellness programs - Other resources, based on eligibility