Clinical Research Associate – Oncology

Excelya

Clinical Research Associate overseeing all aspects of clinical trials to improve patient outcomes at Excelya. Building relationships with study investigators and site staff throughout trial phases.

Posted 7/7/2026full-timeParis • 🇫🇷 FranceJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial processes, site compliance with ICH-GCP guidelines, and effective communication with study sites. Proficient in monitoring patient safety and data integrity while preparing for audits and regulatory inspections.

Highest-signal resume keywords

Clinical Research Associate ExperienceOncology KnowledgeClinical Trial MonitoringClinical Research CertificationFluency in English and French

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Site Initiation VisitsMonitoring VisitsClose-Out VisitsStudy Protocol ComplianceData VerificationPatient Safety MonitoringRegulatory Inspection Preparation

Soft Skills

Effective CommunicationOrganizational SkillsIndependent Work Ability

Certifications & Qualifications

ACRP CertificationSOCRA Certification

Industry Keywords

ICH-GCP GuidelinesClinical Trial ProcessesStudy-Related DocumentsData IntegrityPatient Safety

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

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

What you’ll need

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

Comp & perks

At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.
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.