Senior CRA

ICON; Pavia; In loco; EUR 35.000 - 55.000; Tempo pieno

Descrizione del lavoro

ICON, a leading healthcare intelligence organization, seeks a Senior Clinical Research Associate to oversee clinical trials in Italy. The role involves ensuring compliance with study protocols and collaborating with teams to maintain data integrity and participant safety. Ideal candidates possess significant CRA experience and relevant degrees.

Servizi

Various annual leave entitlements

Health insurance options

Employee Assistance Programme

Life assurance

Flexible country-specific benefits

Competenze

• Extensive experience as a Clinical Research Associate.
• Strong understanding of clinical trial processes.
• Ability to manage multiple sites and projects.

Mansioni

• Monitoring clinical trial sites for adherence.
• Conducting site visits to assess performance.
• Collaborating with cross-functional teams.

Conoscenze

Monitoring practices

Data integrity

Project management

Problem-solving

Communication

Formazione

Laurea Triennale in biotechnology, biology, pharmaceutical sciences

Laurea Magistrale in clinical research-related specializations

Strumenti

Clinical trial software

Descrizione del lavoro

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team in Italy. As a Senior CRA at ICON, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

This role involves working with multiple sponsors, including some of the largest and most high-profile ones.

What You Will Be Doing :

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile :

Laurea Triennale and Laurea Magistrale in a relevant field such as biotechnology, biology, pharmaceutical sciences, or clinical research-related specializations.

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.

Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.

Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.

Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.

Willingness to travel across Italy as part of the position.

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 benefits focused on well-being and work-life balance, including :

Various annual leave entitlements

A range of health insurance options for you and your family

Global Employee Assistance Programme, LifeWorks, offering 24-hour support from over 80,000 professionals

Life assurance

Flexible, country-specific benefits such as childcare vouchers, bike schemes, gym discounts, travel passes, and health assessments

Visit our careers site to learn more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental. We’re committed to providing an inclusive, accessible environment for all candidates. ICON is an equal opportunity employer, considering all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

If you need a reasonable accommodation during the application process or to perform the job functions, please let us know or submit a request here.

Interested but unsure if you meet all requirements? We encourage you to apply — you might be exactly what we’re looking for, whether for this or other roles.

Current ICON employee? Please click here to apply.

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