Senior Clinical Trial Coordinator

ICON Strategic Solutions; Italia; On-site; EUR 31,000 - 38,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Global Employee Assistance Programme (

LifeWorks

Life assurance

Country-specific benefits

Job summary

ICON Strategic Solutions is seeking a Senior Clinical Associate to oversee and support the execution of clinical trials, ensuring quality, compliance, and efficiency. The role emphasizes leading clinical coordination tasks with a focus on continuous improvement and data integrity.

You will manage trial activities, collaborate with cross-functional teams, oversee site management, and provide guidance to clinical staff to ensure adherence to regulatory standards and study protocols.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Significant experience in clinical trial management with regulatory knowledge.
• Ability to manage multiple projects with strong organizational skills.
• Excellent communication and collaboration with diverse teams and stakeholders.
• Detail-oriented with a proactive approach to trial success.

Responsibilities

• Lead clinical coordination tasks with a focus on quality and continuous improvement.
• Manage and coordinate trial activities to meet protocols and timelines.
• Coordinate with cross-functional teams to address issues and optimize processes.
• Oversee site management and data integrity per study protocols.
• Provide guidance to clinical staff and investigators to ensure regulatory compliance.

Skills

Clinical coordination

Project management

Regulatory knowledge

Communication skills

Attention to detail

Independent work

Education

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

Job description

ICON Strategic Solutions is seeking a Senior Clinical Associate to oversee and support the execution of clinical trials, ensuring quality, compliance, and efficiency. The role emphasizes leading clinical coordination tasks with a focus on continuous improvement and data integrity.

You will manage trial activities, collaborate with cross-functional teams, oversee site management, and provide guidance to clinical staff to ensure adherence to regulatory standards and study protocols.