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Remote CRA - Flexible working

Full-time

ICON

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 II with Multi-TA experience.
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
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

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)
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
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

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.
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.
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
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, 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. 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 this form .

Vacancy posted more than 2 months ago
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