Study Start-Up CRA I

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

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.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

What will you be doing?

The Study Start-Up CRA I will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

This role will be dedicated to one sponsor & local sites for Start-Up projects. 

What do you need to have?

Education: Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required

Skills: 

• Read, write and speak upper intermediate English; fluent in host country language required.
• At least 1+ years of Regulatory Start Up experience required
• Knowledge of ICH and local regulatory authority regulations regarding drug
• Clinical research experience is a pluss
• 100% Hombe based position. Available to be hired in any region in Argentina. 

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