IHCRA

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

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As an IHCRA at ICON, you will support the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies.

What You Will Do

You will take responsibility for clinical trial monitoring deliverables, applying your skills to ensure quality and efficiency.

Key Responsibilities Include

What You Will Be Doing:

• Responsible for controlling the contract full details.
• Lead the contract negotiation, and manage site payments.
• Good experience with VeeVa Systems
• Knowledge of Ariba, Apex, RGPS and Grant Plan
• Coordinating the day-to-day operations of clinical studies, including site management, participant recruitment, and data collection.
• Ensuring compliance with Good Clinical Practice (GCP) and regulatory guidelines throughout the study lifecycle.
• Providing training and support to site staff and investigators on study protocols and operational procedures.

Your Profile

• Advanced degree in a relevant field such as life sciences, nursing, or healthcare administration.
• Extensive experience in clinical study coordination or clinical trial management, preferably within the pharmaceutical or biotechnology industry.
• Strong understanding of clinical trial processes, regulatory requirements, and GCP.
• Excellent organizational skills and attention to detail, with the ability to manage multiple studies simultaneously.
• Strong communication and interpersonal skills, with the ability to work collaboratively with diverse teams and stakeholders.

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