As a Senior CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
ResponsibilitiesWhat you will be doing:
Applies knowledge of ICON’s policies and proceduresDemonstrates excellent written and oral communicationDemonstrates excellent knowledge of ICH/GCPDisplays ability to manage investigative sites to facilitate trial deliverablesDemonstrates ability to escalate issues appropriatelyConducts monitoring to confirm subject safety and data integrityDescribes and demonstrates the principals of IP accountabilityIdentifies scientific misconduct at the site levelDemonstrates working knowledge of Microsoft Office applications, Clinical Trial Management Systems, IVRS/IWRS and Electronic Data Capture platformsMentors CRAs new to the position or companyServes as an observation visit leaderConducts monitoring evaluation visitsAssists team lead in the development of trial tools or documentsAssists with CTM tasksParticipates in the development of process changes/improvementsPresents at client meetings/Investigator meetingsProvides training to trial teams Qualifications
You are:
Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience requiredRead, write and speak fluent English; fluent in host country language required.2 years of experience supporting clinical trials including 1 year of on-site monitoring experience (for CRA2); 4 years of experience supporting clinical trials including 3 years of on-site monitoring experience (for CRA3)Ability to travel for approximately 10 site visits each monthProven success monitoring fast paced trials with quick turnaround times for database lockHigh proficiency with Microsoft Office and company collaboration applicationsAdvanced skill in utilization of applicable clinical systemsExperience in monitoring all trial components (PSSV to COV) is preferred
What 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.
Our benefits examples include:
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. 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 through the form below.
https://careers.iconplc.com/reasonable-accommodations
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.