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In this highly specialized and dynamic role, you'll utilise your extensive therapeutic knowledge to oversee uniquely-focused clinical studies. Working at the core of clinical research, you'll be exposed to cutting-edge protocols and experience a dedicated partnership with your team like never before.
What You Will Be Doing
You will monitor multiple Phase I, II, III & IV clinical trial sites across different therapeutic areas. Assist other CRAs with co-monitoring activities both remotely 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 relationships 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 review source data and ensure patient safety and data integrity of the study.
As the first point of contact for study sites, escalate any concerns / issues to relevant departments including Safety, Investigational Medicinal Product, Local Study Managers, and management as appropriate.
You will oversee sites' adherence to GCP / ICH practices, ensuring quality of study conduct.
You Are
Bachelor's Degree (or equivalent) with 3-4 years of relevant clinical monitoring experience
Scientific background
Proficiency with medical terminology
Working knowledge of local regulations
Demonstrated working knowledge of ICH / GCP guidelines
Excellent record-keeping skills and attention to detail
Experience conducting Site Selection, Initiation, Routine Monitoring, and Close Out Visits both remotely and on-site
Fluent in English, both written and oral
Strong technical skills with CTMS, eCRF, eTMF
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 benefits focused on well-being and work-life balance for you and your family.
Our Benefits Examples Include
Various annual leave entitlements
A range of health insurance options for you and your family
Competitive retirement planning offerings
Global Employee Assistance Programme, TELUS Health, with 24-hour access to support professionals
Life assurance
Flexible, country-specific optional benefits such as childcare vouchers, bike schemes, gym discounts, travel passes, health assessments, etc.
Visit our careers website to learn more about working at ICON. ICON values inclusion and belonging, providing an accessible environment for all candidates. We are committed to equal opportunity employment, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
If you're unsure whether you meet all the requirements, we encourage you to apply. You might be exactly who we're looking for, whether for this or other roles.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Pharmaceutical Manufacturing
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