ICON plc

Clinical Python DeveloperAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. Are you passionate about transforming complex clinical data into meaningful insights? Looking to work in a modern tech stack and data pipeline? Join our team as a Clinical Python Developer and play a critical role in driving data-driven decision-making across clinical trials through advanced analytics and visualization solutions. This is your opportunity to make a real impact at the intersection of clinical research, data science, and visualization excellence. What You Will Be Doing: • Be responsible for delivery in a continuous improvement framework with respect to systems deployment, life cycle management and enhancements supported user groups. • Contribute to initiatives to yield faster and more effective report development, efficient change management services for analytics platforms. • Use your technical expertise with clinical data and report building, and experience gained through working with diverse and complex business processes and associated system infrastructures. • Work in a matrix environment across functions and departments. Your Profile: • 4+ years’ experience as a Python Programmer / Visualisation Developer / Business Analyst utilising data warehouse pipelines. • Strong hands-on experience with Python (and relevant libraries/packages) for data transformations and manipulations o Pyspark experience preferred. o Pandas experienced also considered. • Exposure to and understanding of CDSIC guided data structures within a regulated clinical trial environment o Mapping experience and domain specific therapeutic area knowledge preferred. • Solid development skills within Tibco Spotfire or equivalent data visualization tools (Power BI, Tableau, Qlik etc.) • Databricks experience preferred. Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: • 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. Visit our careers site to read more about the benefits ICON offers. 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. Are you a current ICON Employee? Please click here to apply

Site Care Partner - Site Engagement Liaison - Sponsor Dedicated IsraelAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Site Engagement Liaison at ICON, you will foster relationships with clinical trial sites, enhancing site engagement, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You will contribute to clinical research activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: • Building and maintaining strong relationships with key stakeholders at clinical trial sites, including principal investigators, site coordinators, and research staff. • Providing support and guidance to site staff on study protocols, procedures, and regulatory requirements, ensuring compliance and successful study conduct. • Identifying opportunities to improve site engagement and optimize site performance through regular communication and feedback mechanisms. • Collaborating with internal teams to develop and implement site engagement strategies tailored to the specific needs of each study and site. • Monitoring site performance metrics and providing regular updates to study teams on site engagement activities and outcomes. Your Profile: You will bring relevant clinical research experience, along with the following qualifications and skills. Required qualifications and experience: • Bachelor's degree in Life Sciences or a related field. • At least 5 years of experience as a CRA/Senior CRA; CTM experience preferred. • Solid experience managing complex clinical trials across Oncology and non-Oncology therapeutic areas. • Demonstrated experience in study start-up, site activation, study conduct, and close-out activities. • Strong study oversight and site management experience, including prior experience as a site monitor/CRA. • Experience reviewing Monitoring Visit Reports (MVRs) and driving appropriate follow-up actions. • Strong knowledge of ICH-GCP, quality standards, and applicable regulatory requirements. • Strong quality mindset, with a commitment to compliance and inspection readiness. • Excellent communication, stakeholder management, teamwork, organizational, and problem-solving skills. • Fluent in English and Hebrew, with willingness to travel as required (approximately 60%). #LI-Remote #LI-SK1 Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: • 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. Visit our careers site to read more about the benefits ICON offers. 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. Are you a current ICON Employee? Please click here to apply

Clinical Research AssociateAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a CRA II 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 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 Your Profile: You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience: • 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%) • #LI-OB1 Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: • 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. Visit our careers site to read more about the benefits ICON offers. 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. Are you a current ICON Employee? Please click here to apply

Site Specialist II - Israel - Hybrid ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a Site Specialist II at ICON, you will independently manage a range of site support activities, acting as a key operational contact for sites and contribute to efficient study start-up and maintenance. What You Will Do: You will take responsibility for site management and operations deliverables, applying your skills to ensure quality and efficiency. Key responsibilities include: • Coordinating site-level document collection, review, and maintenance, ensuring accuracy and compliance for assigned sites or studies. • Acting as an operational liaison for site staff on documentation, systems, and process-related questions. • Maintaining up-to-date site status, metrics, and key milestones in clinical trial management tools. • Supporting planning and logistics for site meetings, investigator meetings, and monitoring visits. • Identifying opportunities to streamline site workflows and contributing to process improvement initiatives. • Providing guidance to Site Specialist I or junior colleagues, sharing best practices and supporting their development. Your Profile: You will bring relevant site management and operations experience, along with the following qualifications and skills. Required qualifications and experience: • Bachelor's degree in life sciences, healthcare, business, or a related field, or equivalent clinical research experience. • Relevant experience in site support, clinical administration, or similar roles within CRO, pharma, or healthcare. • Prior experience and background in local regulation and ethics • Good understanding of clinical trial processes, GCP, and site documentation requirements. • Exposure to contracts is preferential • Strong organisational and problem-solving skills, with the ability to manage multiple sites and priorities. • Excellent communication and interpersonal skills, with a proactive, service-focused mindset. • Comfort working independently while collaborating effectively with cross-functional teams. Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: • 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. Visit our careers site to read more about the benefits ICON offers. 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. Are you a current ICON Employee? Please click here to apply