Clinical Research Associate II

Pharmaceutical Research Associates, Inc; Bergamo; In loco; EUR 35.000 - 50.000; Tempo pieno

Descrizione del lavoro

A leading company in clinical research is seeking a Clinical Research Associate (CRA) in Italy. The role involves overseeing clinical studies, ensuring compliance with regulations, and collaborating closely with pharmaceutical partners. The ideal candidate has a medical or science degree and 2 years of monitoring experience, eager to work in a fast-paced, impactful environment.

Servizi

Health insurance offerings

Various annual leave entitlements

Competitive retirement planning

Flexible optional benefits

Competenze

• At least 2 years of monitoring experience in phase I-III trials.
• Knowledge of ICH-GCP guidelines.
• Previous monitoring experience in medium-sized studies.

Mansioni

• Set up and monitor studies, complete reports, and maintain documentation.
• Submit protocol and consent documents for ethics approval.
• Assist in training and mentoring fellow CRAs.

Conoscenze

Monitoring experience

Communication in English

Communication in Italian

Ability to work to deadlines

Formazione

Degree in medicine, science, or equivalent

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.

Responsibilities

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

Qualifications

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.Our benefits examples include :

• 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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