Job Description

As a CRA you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence. We are currently looking for a CRA II with Obesity trials experience for one of our FSP programs! What you will be doing: Conduct clinical trial site visits including evaluation, initiation, monitoring and close out Oversee and report on the conduct of clinical trials at a site level including and on-line site visit reports and updates to electronic management systems Proactive site management including: Building and maintaining solid and professional relationships with site staff Facilitating subject enrolment incorporating recruitment strategies and action plans at site level Maintaining site audit/inspection readiness Ensuring appropriate safety reporting and use of on-line safety reporting/reviewing systems Verification of electronic case report form data against written and electronic source documentation as per study schema/monitoring plan Responding to site queries and escalating issues in accordance with processes and timelines Conducting IP accountability and reconciliation Facilitating implementation of new technologies and systems at clinical sites (Electronic Data Capture, eSAE reporting) Maintenance of site study supplies You are: BA/BS/BSc in the sciences or nursing equivalent A trained CRA with at least 2 years of on-site monitoring experience in phase II and phase III trials Working knowledge of Electronic Data Capture (preferred) Experience/working knowledge of the oncology disease area (preferred) Experience of Centralized/Risk Based/Targeted monitoring (preferred) Experience of working within a metric based environment (preferred) Comprehensive knowledge and understanding of ICH-GCP Fluent oral (face to face and telephone) and written English language skills Able and willing to travel up to 60% of the time or as per local requirements Possession of a full driver's license Able and willing to work from a designated and appropriate home office as per local requirements Willing to attend and contribute to team meetings including mandatory training (remote/off-site) Competent computer skills including working knowledge of common software packages Working knowledge of trial management databases and on-line systems Able to attend a 1 week face to face in-house training course as part of on-boarding training Able and willing to work on several protocols/therapy areas Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. _Pay Range ( 110,520.00 USD - 138,150.00USD)_ 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: Various annual leave entitlements A range of health insurance offerings to suit you and your family's needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global 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-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: 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, 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 through the form below. 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. ICON Clinical Research

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