Senior Clinical Research Associate

ICON plc; Italia; Remoto; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A global clinical research company is seeking a Clinical Research Associate for a full-time remote role based in Italy. The ideal candidate will have over 3 years of experience monitoring clinical trials and a relevant degree in Life Sciences or Health Sciences. Responsibilities include ensuring compliance with regulatory requirements, developing study protocols, and engaging in data collection. This position emphasizes independence and attention to detail.

Competenze

• 3+ years of experience as a Clinical Research Associate, monitoring independently across Italy.
• Relevant certification required under Italian law.

Mansioni

• Perform monitoring of clinical trials and ensure compliance with regulatory requirements.
• Develop and maintain study protocols and perform site visits.
• Engage in data collection and contribute to research activities.

Conoscenze

Monitoring clinical trials

Attention to detail

Organizational skills

Ability to work independently

Formazione

Bachelor's / Master's degree in Life Sciences or Health Sciences

Descrizione del lavoro

Since our foundation in Dublin, Ireland in 1990, ICON plc has been dedicated to helping our clients accelerate the development of drugs and medical devices that save lives and improve quality of life. We provide best-in-class information, solutions, and performance with a focus on quality. Operating from a global network of offices in 53 countries, we offer comprehensive consulting, development, and commercialization services. Our innovation centers on critical client needs, such as reducing time to market, cost, and enhancing quality through our extensive expertise in various therapeutic areas.

Role Description

This is a full-time remote role for a Clinical Research Associate. The Clinical Research Associate will perform various tasks including monitoring clinical trials, developing and maintaining study protocols, performing site visits, and ensuring compliance with regulatory requirements. They will engage in data collection, documentation, and contribute to research activities to ensure the successful execution of clinical operations.

Qualifications

• 3+ years of experience as a CRA, monitoring independently across Italy.
• Excellent attention to detail and strong organizational skills.
• Ability to work independently and remotely.
• Relevant certification required under Italian law.
• Bachelor's / Master's degree in a related field such as Life Sciences or Health Sciences.

Additional Opportunities

• Study Operations Manager/ Local Trial Manager - FSP - Remote - Register Your Interest
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