Les missions du poste
About the Job
Excelya is looking for a motivated Clinical Research Associate to join our dedicated Clinical Operations team. As part of our company values of Audacity, Care, and Energy, you will contribute to advancing innovative clinical trials that improve patient outcomes.
In this role, you will oversee all aspects of clinical trials from site initiation to close-out, ensuring compliance with protocols and regulations while building strong relationships with study investigators and site staff.
Key Responsibilities:
- Conduct site initiation visits, monitoring visits, and close-out visits.
- Ensure site compliance with study protocols, ICH-GCP guidelines, and applicable regulations.
- Communicate effectively with study sites to facilitate the trial process and address any issues that arise.
- Review and verify study-related documents and data for accuracy and completeness.
- Monitor patient safety and data integrity throughout the study.
- Assist in preparing for audits and regulatory inspections.
- Provide regular updates to project managers and stakeholders about site progress and challenges.
Le profil recherché
Why Join Us?
At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.
Here's what makes us unique.
We are a young, ambitious health company representing 900 Excelyates, driven to become Europe'sleading mid-size CROwith thebest employee experience. Ourone-stop provider service model offering full-service, functional service provider, and consulting enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient's journey.
Excelling with caremeans benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.
Requirements:
- Experience: Experienced as a Clinical Research Associate, preferably with experience in oncology or related therapeutic areas.
- Education: Bachelor's degree in Life Sciences, Nursing, Pharmacy, or health-related field. Clinical research certification (e.g., ACRP, SOCRA) is a plus.
- Skills: Strong knowledge of clinical trial processes and monitoring; excellent organizational and communication skills; ability to work independently.
- Languages: Fluent in English and French (written and spoken).
Bienvenue chez Excelya
Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of full-service CRO, FSP, and Resourcing solutions guided by our values Energy, Care and Audacity.
Founded in 2014 and headquartered in Paris, France, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas.
We take a one-team approach to work: our shared success is the result of collaboration at every stage of a project, from regulatory affairs and clinical operations to quality assurance and strategic development.
Excelya is committed to helping our clients deliver life-changing therapies collaboratively, so we can transform tomorrow together.
Publiée le 24/04/2026 - Réf : 1d88a8f0-7a91-4acc-b72c-bd5b36c5c518
