IHCRA: Global Clinical Trial Coordinator & Study Manager

ICON Strategic Solutions; Paris; On-site; EUR 40,000 - 65,000; Full time

Benefits offered by this job

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Country-specific benefits (childcare,

Bike purchase schemes, gym discounts,

Job summary

ICON Strategic Solutions seeks an IHCRA to support clinical trial execution and management across sponsor-dedicated programs. You will contribute to advancing innovative therapies by ensuring quality, regulatory compliance, and efficient operations in a global context.

You will monitor trial deliverables, coordinate site management, and train site staff on protocols, with emphasis on adherence to GCP and regulatory guidelines throughout the study lifecycle.

Qualifications

• Advanced degree in life sciences, nursing, or healthcare administration.
• Extensive experience in clinical study coordination or clinical trial management.
• Strong understanding of clinical trial processes, regulatory requirements, and GCP.

Responsibilities

• Coordinate site management, participant recruitment and data collection.
• Monitor trial deliverables, ensuring quality and efficiency in conduct.
• Lead contract negotiation and manage site payments.
• Provide training and support to site staff on study procedures.

Skills

Clinical trial coordination

Regulatory knowledge

Communication skills

Leadership

Education

Advanced degree in life sciences, nursing, or healthcare administration

Tools

Veeva Systems

Ariba

Apex

RGPS

Grant Plan

Job description

ICON Strategic Solutions seeks an IHCRA to support clinical trial execution and management across sponsor-dedicated programs. You will contribute to advancing innovative therapies by ensuring quality, regulatory compliance, and efficient operations in a global context.

You will monitor trial deliverables, coordinate site management, and train site staff on protocols, with emphasis on adherence to GCP and regulatory guidelines throughout the study lifecycle.