Icon plc is a world-leading healthcare intelligence and clinical research organisationFrom 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 successIcon people have a mission to succeed and a passion that ensures what we do, we do well.
You are a forward thinkerYou are an innovator that refuses to settleYou want to push the boundaries and change not just what it means to be a clinical research associate, you want to change the futureYou want to learn from the best, grow your knowledge and your skill set, and you want to build your career hereYou want to use the latest technology and tools in the industry to push the momentum of an already growing company forwardYou want to find a balance that still lets you be, well, youMost of all, you want to do it in a place where you’re more than an employee numberA place you love workingStill here? goodBecause if this is you, we’d really like to meet you.
Responsibilities
As a clinical research associate (cra), you will monitor the progress of clinical studies, either 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.
Qualifications
What do you need to have?
Undergraduate degree or its international equivalent in clinical, science, or health related field from an accredited institution; a licensed healthcare professional (i.e., registered nurse); or equivalent work experience required
2+ years of clinical monitoring experience or equivalent combination of education and experience is required for the level 2 role; 5+ years is required for a level 3
Ability to travel
Knowledge of ich and local regulatory authority regulations regarding drug trials
To qualify, applicants must be legally authorized to work in the united states, and should not require, now or in the future, sponsorship for employment visa status.
Benefits of working in icon:
Our success depends on the knowledge, capabilities and quality of our peopleThat’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
At icon, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programsIn addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
Icon, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassmentAll 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.
Options
Apply Now onlineapply share sorry the share function is not working properly at this momentPlease refresh the page and try again laterShare on your newsfeed
Connect with us!
