Senior CRA: Lead Monitoring & Site Ops

ICON Strategic Solutions; Paris; Sur place; EUR 70 000 - 95 000; Plein temps

Avantages offerts par ce poste

Health insurance

Life assurance

Retirement planning

Employee assistance

Résumé du poste

ICON plc is a leading healthcare intelligence and clinical research organization seeking a Clinical Research Associate to lead monitoring tasks with a focus on quality and continuous improvement. The role requires overseeing site visits, regulatory compliance, and data reporting across multiple sites.

You will collaborate with cross-functional teams, guide site staff, and travel up to 60% to ensure trial success while upholding ICON’s commitment to inclusive work practices and high standards of

Qualifications

• Strong foundation in clinical trial monitoring and QA
• Experience as a Clinical Research Associate with regulatory knowledge
• Ability to manage multiple sites and projects
• Proficiency in data integrity and site management
• Excellent communication and stakeholder management skills
• Willingness to travel approximately 60%

Responsabilités

• Monitor clinical trial sites to ensure adherence to study protocols and GCP standards.
• Conduct site visits to assess performance, resolve issues, and support trial execution.
• Collaborate with cross-functional teams to ensure accurate data collection and reporting.
• Provide training and guidance to site staff to maintain high trial conduct standards.
• Build and maintain relationships with site personnel and stakeholders for smooth operations.

Connaissances

Independent worker

Stakeholder management

Communication

Problem solving

Travel readiness

Formation

Bachelor's degree in a relevant field

Outils

Clinical trial software

Description du poste

ICON plc is a leading healthcare intelligence and clinical research organization seeking a Clinical Research Associate to lead monitoring tasks with a focus on quality and continuous improvement. The role requires overseeing site visits, regulatory compliance, and data reporting across multiple sites.

You will collaborate with cross-functional teams, guide site staff, and travel up to 60% to ensure trial success while upholding ICON’s commitment to inclusive work practices and high standards of