Senior Clinical Research Associate

ICON Strategic Solutions; Italia; In loco; EUR 45.000 - 65.000; Tempo pieno

Vantaggi offerti da questo lavoro

Health insurance

Competitive salary

Various annual leave entitlements

Global Employee Assistance Programme

Flexible optional benefits

Descrizione del lavoro

ICON Strategic Solutions is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trial activities in Italy. The role involves monitoring trial sites, ensuring compliance with protocols, and supporting team collaboration.

The successful candidate will have an advanced degree, extensive CRA experience, and strong organizational skills. Benefits include competitive salary, health insurance, and assistance programs to support work-life balance.

Competenze

• Extensive experience as a Clinical Research Associate with regulatory knowledge.
• Proven ability to manage multiple sites and projects simultaneously.
• Ability to travel at least 60% of the time.

Mansioni

• Monitor clinical trial sites for adherence to protocols and GCP standards.
• Conduct site visits for performance assessment and support.
• Collaborate with teams for timely data collection.
• Provide training to site staff and CRAs.
• Build relationships with stakeholders for trial operations.

Conoscenze

Clinical trial processes

Data integrity

Site management

Organizational skills

Communication skills

Formazione

Advanced degree in life sciences, nursing, or medicine

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. As a Senior CRA at ICON Plc, 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.

Responsibilities

• 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

• Advanced degree in a relevant field such as life sciences, nursing, or medicine.
• 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.
• Ability to travel at least 60% of the time (international and domestic) and should possess a valid driver’s license.
• Location: Rome, Venice or Florence.

What ICON Can Offer You

• Competitive salary and a range of benefits designed to support well-being and work-life balance.
• Various annual leave entitlements and health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of professionals for well-being support.
• Life assurance and flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, and health assessments.

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

At 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, color, 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 or submit a request here.

Interested 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.

Are you a current ICON Employee? Please click here to apply