Clinical Research Associate II

ICON; Ancona; In loco; EUR 30.000 - 50.000; Tempo pieno

Descrizione del lavoro

ICON recherche un Clinical Research Associate basé à Ancona, Italie, pour rejoindre une organisation de recherche clinique de premier plan. Le poste implique la mise en place et le suivi d'études tout en collaborant avec des entreprises pharmaceutiques. Les candidats doivent avoir au moins 2 ans d'expérience en surveillance d'essais cliniques et un diplôme pertinent. ICON offre une culture inclusive, des atouts de formation, et diverses prestations pour soutenir le bien-être.

Servizi

Congés annuels

Assurance santé

Plan de retraite compétitif

Programme d'assistance aux employés

Assurance vie

Avantages optionnels divers

Competenze

• Minimum 2 ans d'expérience en surveillance d'études cliniques phase I-III.
• Expérience en études de taille moyenne, y compris démarrage et clôture.
• Disponibilité à voyager au moins 60% du temps.

Mansioni

• Travailler de manière indépendante pour mettre en place et suivre des études.
• Préparer et soumettre des documents pour approbation éthique.
• Responsabilité pour l'efficacité des coûts des études.

Conoscenze

Moniteur d'études cliniques

Communication écrite et verbale

Connaissances des directives ICH-GCP

Gestion du temps

Formazione

Diplôme en médecine ou science

Descrizione del lavoro

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.

As a CRA in Italy you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

You will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people's lives. Working in this program you will feel challenged and supported to advance in your professional career while making a truly impact.

What you will be doing :

• Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
• Submitting protocol, consent documents for ethics / IRB approval, as well as preparing regulatory submissions
• Taking responsibility for study cost efficiency
• Preparation and review of study documentation and feasibility studies for new proposals
• Potential to assist in training and mentoring fellow CRAs

You are :

• At least 2 years of monitoring experience in phase I-III trials as a CRA
• Degree in medicine, science, or equivalent
• Previous monitoring experience in medium-sized studies, including study start-up and close-out
• Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
• Excellent written and verbal communication in both English and Italian
• Ability to work to tight deadlines
• Availability to travel least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license

What ICON can offer you :

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON : ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, 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 through the form below.

in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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Clinical Research Associate • ancona, Italia