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Clinical Research Coordinator

  1. Piedmont
JR088342
  1. ICON Full Service & Corporate Support
  2. Clinical Research Site Services

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 organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation 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.

The role:
The Clinical Research Coordinator (CRC) will coordinate and ensure execution of all clinical study protocol activities within Good Clinical Practice (GCP) and the Food and Drug Administration (FDA) regulations and requirements, Sponsor expectations and ICON Early Phase Standard Operating Procedures (SOPs). The CRC will work with study Principle/Sub Investigators (Sub-PI), Study Managers and Clinical Manager for project scheduling and design. The CRC should have a basic understanding of research methods and various research study design to identify and ensure successful clinical studies preparation, site initiation, monitoring and closeout visits.

You will need:
• We are seeking candidates with a Bachelor’s degree in a related field OR Certified/Registered Medical Assistant (CMA/RMA), Licensed Vocational Nurse (LVN), Registered Nurse (RN), Emergency Medical Technician (EMT).
• Two years medical experience
• Previous research experience
• Proficient with Microsoft Office
• Certified Clinical Research Coordinator (CCRC) preferred

Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. 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 the form below.

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