Les missions du poste
About the Job
Excelya invites you to join a team defined by Audacity, Care, and Energy. We foster bold innovation and support a collaborative environment where personal and professional growth thrive.
As a Clinical Research Associate at Excelya, you will be integral to ensuring the successful execution of clinical trials by overseeing site activities, adherence to protocols, and regulatory compliance. This role is pivotal in advancing clinical projects that aim to improve patient care.
Main Responsibilities:
- Conduct site initiation, monitoring, and close-out visits to ensure compliance with clinical trial protocols.
- Maintain effective communication with investigators and site staff to support trial progress.
- Review and verify clinical trial data and documentation for accuracy and completeness.
- Monitor patient safety and data integrity throughout the study duration.
- Assist in preparation for audits and inspections, ensuring sites are inspection-ready.
- Report deviations, adverse events, and other study-related issues in a timely manner.
- Collaborate with project managers to provide updates and address challenges encountered at sites.
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:
- 1-3 years of experience as a Clinical Research Associate, preferably in oncology or other therapeutic areas.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related field; advanced degrees or certifications in clinical research are advantageous.
- Strong knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.
- Excellent interpersonal, communication, and organizational skills.
- Fluency in English and French.
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 13/05/2026 - Réf : 49b4cd00-0b97-438a-a2c3-c319ac2ccd89
