Senior Clinical Trial Associate - Lead Trial Operations

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

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,