• implementation of research projects: creating offers and research concepts, analysis of results, preparation of a report, presentation of results • establishing and maintaining contacts with clients • active participation in proposing research solutions • participation in the implementation of sales and development goals of the department • readiness to promote NEUROHM methods at conferences, industry events • cooperation with the team on new products

• Design and conduct qualitative and quantitative market and product research studies to identify market trends, understand customer needs, validate product concepts, and assess usability • Serve as the internal expert on Customer Insights (CI) and Market Research topics • Perform and leverage competitive analyses, product benchmarking, and user experience evaluations to inform product positioning and differentiation • Collaborate with cross-functional teams to translate research findings into concrete product requirements and innovation strategies • Produce clear, compelling reports and presentations to communicate insights and recommendations to organizational stakeholders

Clinical Research Associate 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 We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II 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. What you will be doing - 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 - Work location: Home-based Your profile - Bachelor's degree in a scientific or healthcare-related field - Minimum of 2 years of Global SIT Phase I to III onsite monitoring CRA experience - 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 #LI-DP1 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

• Utilize your analytical and quantitative skills, market knowledge and intuition to develop and implement automated statistical trading models. • Participate in all aspects of research and trading model development, including generating research ideas, building and analyzing data sets, conducting statistical data analysis and implementing quantitative production trading models.