{"id":3050827,"url":"https://alion.io/job/icon-clinical-research-associate-3-2","title":"Clinical Research Associate 3","company":{"id":5677,"name":"ICON","domain":"iconplc.com","url":"https://alion.io/company/icon","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":null},"role":"Biotech","role_family":"Biotech","seniority":null,"employment_type":"full_time","work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"board_field","remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Sydney, Australia"],"countries":["AU"],"hiring_countries":["AU"],"hiring_countries_total":1,"salary":null,"salary_estimate":null,"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false},{"name":"Good Clinical Practice","optional":false}],"status":"live","first_seen_at":"2026-10-22T02:26:09Z","employer_posted_date":"2026-10-22","last_verified_at":"2026-10-22T03:45:51Z","board_verified":true,"closed_at":null,"days_open":0,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":0},"description":"CRA III Adelaide, Australia - RemoteAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.\nAs 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.\nAs a Senior 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.\nWhat You Will Do:\nYou will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.\nKey responsibilities include:\nMonitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.\nConducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.\nCollaborating with cross-functional teams to ensure timely and accurate data collection and reporting.\nProviding training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.\nBuilding and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.\nYour Profile:\nYou will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.\nRequired qualifications and experience:\nBachelor's degree in a relevant scientific discipline or healthcare-related field\nExtensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.\nProven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.\nExpertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.\nExcellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.\nWillingness to travel as required (approximately 60%)\nEmployment with ICON is contingent upon having the legal right to work in the country where the role is based.\nRewards & Benefits\nICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.\nBenefits may include:\nCompetitive base salary and performance related incentives\nHealth and wellbeing programmes including medical, dental, and vision coverage where applicable\nRetirement and pension plans\nLife assurance and disability coverage\nEmployee assistance programmes and wellbeing resources\nLearning and development opportunities through structured training and career pathways\nBenefits may vary depending on role and location.\nVisit our careers site to read more about the benefits ICON offers.\nInclusion and Accessibility\nICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.\nIf you require reasonable accommodations during the recruitment process, please let us know or submit a request here.\nAre you a current ICON Employee? 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