Senior Clinical Research Associate
Senior CRA / CRA II
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
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Overview:
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.
DESCRIPTION DU POSTE
ICON plc est une organisation de recherche clinique et d’intelligence en soins de santé de premier plan à l’échelle mondiale. De la molécule à la médecine, nous faisons progresser la recherche clinique en offrant des services externalisés aux entreprises pharmaceutiques, biotechnologiques et d’équipement médical, ainsi qu’aux organismes gouvernementaux et de santé publique.
En maintenant nos patients au centre de toutes nos activités, nous aidons à accélérer le développement des médicaments et des dispositifs qui sauvent des vies et améliorent la qualité de vie.
Nos employés sont au cœur de notre culture et constituent la force motrice de notre succès. Les employés d’ ICON ont pour mission de réussir et leur passion garantit que nous faisons bien notre travail.
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.
Responsabilités
En tant qu’associé(e) de recherche clinique (ARC), vous surveillerez les progrès des études cliniques aux centres d’étude ou à distance, et vous vous assurerez que les études cliniques sont menées, documentées et signalées conformément au protocole, aux procédures opérationnelles normalisées (PON), aux bonnes pratiques cliniques (BPC) élaborées par la Conférence internationale sur l’harmonisation (CIH) et à toutes les exigences réglementaires applicables.
Qualifications:
What do you need to have?
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Bachelor's degree, or its international equivalent in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role
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1+ years of clinical monitoring experience or equivalent combination of education and experience is required for the level 2 role; 3+ years is required for a level 3
- ONCOLOGY MONITORING EXPERIENCE PREFERRED
- ABILITY TO TRAVEL 70%
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Knowledge of ICH and local regulatory authority regulations regarding drug trials
To qualify, applicants must be legally authorized to work in the United States or Canada, 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 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, suppo