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.
The Role:
The Research Assistant is integral in the execution of all aspects of the clinical trial, will have direct patient contact and is responsible for ensuring that all clinical trial activities are performed as outlined by the clinical trial protocol. As a Research Assistant, you will also be responsible for performing the task(s) as per clinical trial protocol, ICON Early Phase Services SOPs, FDA, ICH GCP, and utilizing proper source documentation techniques; and participate in clinical trial meetings and training as warranted by the study protocols.
To be successful in the role, you will have:
- Minimum of one-year experience in clinical research or related fields.
- High School Diploma or equivalency with medical assistant training/certification or other allied health certification
- Medical Assistant, Phlebotomy Technician, Paramedic, EMT, LVN, or RN preferably with two years of experience;
- Maintains current job-related competencies, certifications, and/or licensure.
