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.
Requirements
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).
Benefits
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’s leading mid-size CRO with the best employee experience. Our one-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 care means 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.
Other open roles at Excelya(6)
Excelya is an independent, Paris-headquartered contract research organization (CRO) founded in 2014 that supports biotech, pharmaceutical, and medical device companies with full-service CRO, FSP, and resourcing solutions across clinical development. The company operates through a global network with 900+ experts and coverage in 25 countries, offering capabilities in areas such as clinical operations, data management, biometrics, pharmacovigilance, regulatory affairs, and medical affairs to help clients deliver clinical trials and bring new therapies to patients.
Key team members
Julien Sallaind
Elitza Ouzounova
Emilie Stefanelli
Laurence MAUNIER
Jobr aggregates jobs directly from company career portals — no middlemen. Our team applies on your behalf with AI-tailored resumes, reviewed by a human before submission.