CRC Level 1
- Wilmington
- ICON Full Service & Corporate Support
- Clinical Research Site Services
- Office Based
About the role
This vacancy has now expired. Please click here to view live vacancies.
At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.
Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
Overview of the role:
Title: Clinical Research Coordinator I
Location: On-Site, Wilmington NC
Summary: As a Clinical Research Coordinator within our team, you will be overseeing coordinating our procedural tasks and documentation for our clinical trials running on-site. Our mission within this group is to bring clinical research to as many lives as possible, while delivering unparalleled service and exceptional value to our clinical trial partners.
Duties:
- Participate in the early planning phases of clinical study by providing assistance in the preparation of study proposal timelines, scheduling and other study requirements as appropriate
- Evaluate, coordinate, and ensure the completion of all protocol related tasks
- Coordinate with Study or Project Manger to ensure appropriate timelines are being met as per contractual obligations
- Participate in meetings to include (pre-planning and clinical tracking).
- Coordinates with Screening and Recruitment to maintain timely execution of study enrolment
Role Requirements:
- Bachelor’s Degree in medicine, science or equivalent degree would be desirable but not essential
- Excellent communication, planning and decision-making skills
- Must be able to utilize computer-based applications such as Microsoft Office and other web based systems including CTMS systems
Benefits of Working in ICON:
ICON provides you with the innovative resources to be successful in delivering results, inspiring others and becoming a trusted partner. We offer an exceptional benefits package that includes a comprehensive health plan, retirement plans, highly competitive pay, corporate bonus plan, time away from work, and many other incentives amongst an opportunity to grow your career within ICON.
What’s Next?
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
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