Clinical Research Associate Jobs at ICON, France | Life Sciences Candidates, Apply Online
A rare chance has emerged for aspiring Clinical Research Associates in Paris, France. ICON, a global leader in healthcare intelligence and clinical research, is seeking qualified candidates for Clinical Research Associate Jobs. This role offers an opportunity to contribute to clinical trial operations while working in a collaborative environment.
- Job Title: Clinical Research Associate I
- Location: Paris, France
- Reference Number: JR161852
- Work Type: Office-based with flexibility, remote or office
About The Company
ICON is a global healthcare intelligence and clinical research organization committed to bringing new medicines and treatments to patients faster. With a strong emphasis on integrity, collaboration, agility, and inclusion, ICON operates in various locations, including Paris, France, where they are currently hiring for the Clinical Research Associate I position.
Clinical Research Associate Jobs: Job Description
As a Clinical Research Associate I at ICON, the candidate will play a crucial role in the clinical trial operations function. This position, part of the Clinical Research Associate Jobs at ICON, requires individuals to be based in the Paris area and will involve national travel. The CRA I will be responsible for delivering high-quality outcomes across clinical programs while ensuring patient safety and protocol compliance.
Key Responsibilities
- Coordinate activities related to study set-up and monitoring, maintaining accurate study documentation and status reports.
- Conduct monitoring visits in accordance with study protocols, ICH-GCP guidelines, and applicable regulatory requirements.
- Efficiently run sponsor-generated queries and support timely issue resolution.
- Contribute to the preparation and review of study documentation and feasibility assessments for new proposals.
- Develop and maintain strong collaborative relationships with clinical investigators, site staff, and key stakeholders.
- Ensure patient safety, protocol compliance, and data integrity throughout the study lifecycle.
- Support study delivery through effective site management and communication.
Eligibility Criteria Required For Clinical Research Associate Jobs
- University degree in Life Sciences, or an equivalent scientific discipline.
- Minimum 1 year of independent clinical trial monitoring experience as a CRA.
- Experience conducting site monitoring visits and managing study sites independently.
- Knowledge of ICH-GCP guidelines and the ability to review and evaluate clinical data.
- Excellent written and verbal communication skills in English and French.
- Strong interpersonal skills with the ability to manage site relationships and resolve queries effectively.
- Strong organizational skills and attention to detail.
- Willingness to travel as required (approximately 60%).
- Residency in the Paris area.
Why Join ICON?
ICON values the quality of its people and has prioritized building a diverse culture that rewards high performance and nurtures talent. In addition to a competitive salary, ICON offers a range of benefits focused on well-being and work-life balance opportunities for employees and their families. The organization is committed to providing an inclusive and accessible environment for all candidates, ensuring equal consideration for all roles without discrimination.
In summary, ICON is offering a valuable opportunity for qualified Clinical Research Associates in Paris. Those seeking Clinical Research Associate Jobs are encouraged to apply as soon as possible to be considered for this role.
