Senior Clinical Trial Associate

ICON Strategic Solutions; France; Sur place; EUR 50 000 - 70 000; Plein temps

Avantages offerts par ce poste

Annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Résumé du poste

ICON plc is a world-leading healthcare intelligence and clinical research organization. The Senior Clinical Trial Associate role involves taking ownership of clinical trial management deliverables and providing administrative support to ensure trial success.

You will collaborate with cross-functional teams to maintain compliance, documentation, and site communications, with travel up to ~10%. You will work in an environment that values inclusion, excellence, and a patient-centric approach,

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Extensive experience in a clinical trial support role with understanding of processes and regulatory requirements.
• Strong organizational and multitasking skills; ability to manage multiple tasks and projects.
• Proficiency in CTMS and regulatory/documentation software; meticulous data handling.
• Excellent communication and collaboration skills with diverse teams and stakeholders.
• Willingness to travel (approximately 10%).

Responsabilités

• Provide administrative support for clinical trials, manage documentation, coordinate meetings, and maintain trial records.
• Assist in preparation and submission of regulatory documents, ensuring compliance with study protocols and regulatory requirements.
• Collaborate with cross-functional teams to support trial operations and resolve issues.
• Monitor trial progress and site communications; ensure timely delivery of study materials.
• Build and maintain strong relationships with site staff and other stakeholders to support trial operations.

Connaissances

Clinical trial management

Documentation and data management

Regulatory compliance

Communication skills

Travel willingness

Formation

Bachelor's degree in a relevant scientific discipline

Outils

CTMS (clinical trial management systems)

Regulatory submission tools

Description du poste

Senior CTA

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.

As a Senior Clinical Trial Associate at ICON Plc, you will support the management and execution of clinical trials by handling a range of administrative and operational tasks.

What You Will Do

You will take ownership of clinical trial management deliverables, applying your expertise to complex challenges.

Key Responsibilities Include

• Providing administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records.
• Assisting in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements.
• Collaborating with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study.
• Monitoring and tracking trial progress, including managing site communications and ensuring timely delivery of study materials.
• Building and maintaining strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support overall project success.

Your Profile

You will have a strong foundation in clinical trial management, 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 in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements.
• Strong organizational and multitasking skills, with the ability to manage multiple tasks and projects effectively.
• Proficiency in clinical trial management systems and relevant software, with a keen eye for detail in documentation and data management.
• Excellent communication, interpersonal, and problem-solving skills, with the ability to work collaboratively with diverse teams and stakeholders.
• Willingness to travel as required (approximately 10%)

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.

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