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 an In-House Clinical Research Associate (IHCRA) to join our diverse and dynamic team. As an IHCRA at ICON, you will play a pivotal role in supporting the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies.This role is office based in Barcelona or Madrid (Hybrid). Applicants must be able to commute to either office.What You Will Be Doing Assisting in the planning, initiation, and execution of clinical trial activitiesConducting site feasibility assessments and participating in site selection processesCoordinating with investigative sites to ensure compliance with study protocols and regulatory requirementsMonitoring study progress and data collection activities to ensure quality and accuracyAssisting in the preparation and review of study documentation and reportsYour profile Bachelors degree in a relevant field, such as life sciences or healthcarePrevious experience in clinical research or a related field preferredStrong organizational and communication skillsAbility to work independently and collaboratively in a fast-paced environmentAttention to detail and ability to prioritize tasks effectivelyWhat 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.Various annual leave entitlementsA 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.General Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.Life assuranceFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized 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 hereInterested 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 applyQuality Assurance Officer of GCPs for Clinical Development RADeep Study Coordinator (Childhood cancer and blood disorders) Clinical Validation & Pilot Studies Coordinator (Re2) Clinical Research Coordinator (at the rank of Senior Technical Officer/Technical Officer) in the Clinical Research Centre Manager, Quality Management Documentation and Quality Management Systems - Europe - Remote Research Associate/Senior Research Associate- National Centre of Excellence in Intellectual Disability Health Freelance Senior Manager, Quality Assurance (GCP Auditor) (0.8-1.0 FTE) Clinical Project Manager ( Medical Devices) Global Clinical Project Manager - Vendor Management Expert - Novartis Dedicated (home-based in Europe)#J-18808-Ljbffr