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.As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing :
You will monitor multiple Phase II, III clinical trial sites, across different therapeutic areas. Assist other CRAs with co-monitoring activities both remote and on-site.You will utilise your customer service mindset with your sites focusing on delivering value, building loyalty and trust to create a positive impact and strong relationship with investigators and study coordinators where respect, knowledge and commitment to ICH / GCP guidelines are key to successful trial conduct.As the CRA you are the main sponsor representative, providing key project updates. You will collaborate with the team, developing commitment to study timelines and objectives through regular visits with site staff in-person and remotely.You will be first to review "source to CRF / eCRF," ensuring patient safety and data integrity aspect of the study.As the first point of contact for study sites, escalating any concerns / issues to other departments including Safety, Investigational Medicinal Product, Local Study Managers and management team as appropriate.Additionally, you will oversee the sites' adherence to GCP / ICH practices, ensuring quality of study conduct.You are :
Bachelor’s Degree (or equivalent) with 2-4 years of relevant healthcare experience in the pharma or clinical research industry. Minimum 2 years of monitoring and site management experienceScientific backgroundProficiency with medical terminologyWorking knowledge of Local RegulationsA demonstrated working knowledge of ICH / GCP GuidelinesExcellent record-keeping skills and attention to detailExperience conducting Site Selection, Initiation, Routine Monitoring and Close Out Visits both remotely and on-siteFluent in English, both written and oralStrong technical skills with CTMS, eCRF, eTMFWhat 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 needsCompetitive retirement planning offerings to maximise savings and plan with confidence for the years aheadGlobal 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-beingLife assuranceFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among othersICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, 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.J-18808-Ljbffr
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