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.
Requirements
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.
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
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