Provide safety monitoring and supervision of study participants.Īdminister investigational drugs and concomitant medications to subject according to study protocol.Įnsure proper documentation to meet all reporting requirements.ĭemonstrate strong ethical and safety practices. Maintaining nursing knowledge, skills and licensure. Lastly, because research is all about the documentation, you’ll be documenting all of the data you collect and work closely with study investigators on any adverse events that may happen.Ĭlinical Quality, Data Integrity, and Safety You will administer study drugs, take vitals, perform phlebotomy and conduct other examinations given by the study protocol. You will be working side-by-side with research associates collecting data from our subjects, while also using your RN /LPN experience to keep those subjects safe. ICON people have a mission to succeed and a passion that ensures what we do, we do well.Īs a Clinical Research Nurse, you are helping with the overall execution of Phase 1 clinical trials. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

ICON plc is a world-leading healthcare intelligence and clinical research organisation.

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