Clinical Associate

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.- The role:
- As Clinical Associate you would be an integral part of the study team whilst acquiring clinical and corporate knowledge of clinical trial conduct. Provide administrative support to the Project Manager(s), Clinical Trial Manager(s) and/or sites, with emphasis on driving global inspection readiness.- You will need:- Bachelor’s degree preferred in a scientific/medical discipline or equivalent experience.
- An understanding of Pharmaceutical industry process with previous exposure to medical terminology and GCPs is preferred.
- You will possess good written and verbal communication in EnglishBenefits of Working in ICON:
- 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.- The role:
- As Clinical Associate you would be an integral part of the study team whilst acquiring clinical and corporate knowledge of clinical trial conduct. Provide administrative support to the Project Manager(s), Clinical Trial Manager(s) and/or sites, with emphasis on driving global inspection readiness.- You will need:Bachelor’s degree preferred in a scientific/medical discipline or equivalent experience.
-An understanding of Pharmaceutical industry process with previous exposure to medical terminology and GCPs is preferred.
You will possess good written and verbal communication in English

Benefits of Working in ICON:
- Our success depends on the knowledge, capabilities and quality of our people. That'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 programs. In 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 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. #LI-ED1- #LI-Remote