Clinical Research Associate

divh2Clinical Research Associate - California/h2pICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster./ppAs 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./ppAs a CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards./ppWhat You Will Do:/ppYou will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include:/pulliMonitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards./liliConducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution./liliCollaborating with cross-functional teams to ensure timely and accurate data collection and reporting./liliProviding training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct./liliBuilding and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations./li/ulpYour Profile:/ppYou will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience:/pulliBachelors degree in a relevant scientific discipline or healthcare-related field/liliExtensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements./liliProven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills./liliExpertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools./liliExcellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment./liliWillingness to travel as required (approximately 60%)/li/ulpEmployment with ICON is contingent upon having the legal right to work in the country where the role is based./ppRewards Benefits/ppICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development./ppBenefits may include:/pulliCompetitive base salary and performance related incentives/liliHealth and wellbeing programmes including medical, dental, and vision coverage where applicable/liliRetirement and pension plans/liliLife assurance and disability coverage/liliEmployee assistance programmes and wellbeing resources/liliLearning and development opportunities through structured training and career pathways/li/ulpBenefits may vary depending on role and location./ppInclusion and Accessibility/ppICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported./ppIf you require reasonable accommodations during the recruitment process, please let us know or submit a request here./p/div