Clinical Research Associate II
2 weeks ago
As a Clinical Research Associate II, you will be part of a dynamic team responsible for monitoring clinical trials across various therapeutic areas. Your primary focus will be on ensuring the quality and integrity of trial data, while maintaining strong relationships with investigators and study coordinators.
Key Responsibilities:- Monitor multiple clinical trial sites, conducting regular visits to ensure compliance with ICH/GCP guidelines.
- Collaborate with the team to develop and implement study timelines, ensuring timely completion of trial objectives.
- Review and verify source data, ensuring accuracy and integrity of trial results.
- Escalate any concerns or issues to relevant departments, ensuring prompt resolution and minimizing trial delays.
- Oversee site adherence to GCP/ICH practices, ensuring high-quality trial conduct.
- Bachelor's Degree (or equivalent) with 2-4 years of relevant healthcare experience in the pharma or clinical research industry.
- Minimum 12 months of independent clinical trials monitoring experience and site management experience.
- Scientific background and proficiency with medical terminology.
- Working knowledge of Local Regulations and ICH/GCP Guidelines.
- Excellent record-keeping skills and attention to detail.
- Experience conducting Site Selection, Initiation, Routine Monitoring, and Close Out Visits.
- Fluent in English, both written and oral.
- Strong technical skills with CTMS, eCRF, and eTMF.
At ICON, we value diversity, inclusion, and belonging. Our team is committed to providing an inclusive and accessible environment for all candidates. We offer a competitive salary, a range of benefits, and opportunities for professional growth and development.
Our benefits include various annual leave entitlements, health insurance, retirement planning, and a global Employee Assistance Programme. We also offer flexible country-specific optional benefits, such as childcare vouchers, bike purchase schemes, and discounted gym memberships.
Visit our careers website to learn more about the benefits of working at ICON: https://careers.iconplc.com/benefits
We are an equal opportunities employer and welcome applications from all qualified candidates. If you need a reasonable accommodation for any part of the application process, please let us know through the form below: https://careers.iconplc.com/reasonable-accommodations
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