Senior Clinical Research Associate

ICON San Antonio; Milano; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

ICON Strategic Solutions is seeking a Clinical Research Associate to lead monitoring activities with a focus on quality and continuous improvement. You will conduct site visits, ensure adherence to GCP and regulatory standards, and support successful trial execution through collaboration with cross-functional teams.

The role requires guiding site staff, managing multiple sites, and travelling up to 60% to ensure data integrity and high standards of conduct across trials.

Competenze

• Bachelor's degree in a relevant scientific field.
• Extensive experience as a Clinical Research Associate with regulatory knowledge.
• Ability to manage multiple sites and projects concurrently.
• Expertise in monitoring, data integrity and site management.
• Strong communication and stakeholder management skills.

Mansioni

• Lead clinical trial monitoring tasks with a focus on quality and continuous improvement.
• Perform site visits, assess performance, resolve issues and support trial execution.
• Collaborate with cross-functional teams to ensure timely data collection and reporting.
• Provide training and guidance to site staff to maintain high trial conduct standards.
• Build and maintain effective relationships with site personnel and stakeholders.

Conoscenze

Clinical trial monitoring

Regulatory compliance

Site management

Data integrity

Communication & stakeholder mgmt

Travel readiness

Formazione

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Strumenti

CTMS

Descrizione del lavoro

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

What You Will Do

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.

Key Responsibilities Include

• 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

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.

Required Qualifications And Experience

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• 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 as required (approximately 60%)

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 maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others.

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