IHCRA

ICON Strategic Solutions; Paris; Sur place; EUR 50 000 - 70 000; Plein temps

Avantages offerts par ce poste

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible optional benefits

Résumé du poste

ICON Strategic Solutions in Paris is seeking an experienced in-house CRA to manage clinical study operations, ensuring compliance with regulatory standards. This role involves overseeing day-to-day operations, including participant management and data collection, while contributing to innovative treatment advancements.

You will require an advanced degree in life sciences or healthcare administration and extensive clinical study coordination experience. ICON offers a range of benefits focused on work-life balance and well-being for employees and their families.

Qualifications

• Extensive experience in clinical study coordination or trial management, preferably in pharma or biotech.
• Strong understanding of clinical trial processes and GCP.
• Ability to manage multiple studies simultaneously.

Responsabilités

• Control and manage contract details and site payments.
• Coordinate day-to-day operations including participant recruitment.
• Ensure compliance with GCP and regulatory guidelines.

Connaissances

Clinical study coordination

Regulatory compliance

Communication skills

Organizational skills

Team collaboration

Formation

Advanced degree in life sciences, nursing, or healthcare administration

Outils

VeeVa Systems

Ariba

Apex

RGPS

Grant Plan

Description du poste

CTC Finance

ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking an in‑house CRA to join our diverse and dynamic team. As a IHCRA at ICON, you will play a pivotal role in the planning, execution, and oversight of clinical studies, ensuring that they are conducted in compliance with regulatory requirements and protocols. You will contribute to the advancement of innovative treatments and therapies by facilitating effective study operations and enhancing participant engagement.

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.

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, subsidised travel passes, health assessments, among others.

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.