Clinical Research Associate H/F Excelya
- Paris - 75
- CDI
- Bac +5
- Industrie Pharmaceutique • Biotechn. • Chimie
- Exp. 3 ans min.
Les missions du poste
Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.
As a Clinical Research Associate (CRA), you will be responsible for monitoring clinical studies and ensuring compliance with study protocols, ICHGCP guidelines, and regulatory requirements. You will act as a key liaison between study sites and project teams, contributing to the successful execution of oncology clinical trials.solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.
Key Responsibilities
- Review study protocols and provide operational feedback regarding site implementation and study feasibility.
- Contribute to the development of study documentation, including CRFs, monitoring guidelines, investigator brochures, and study materials.
- Collect and review all site documentation required for study startup activities.
- Plan and perform site initiation, monitoring, and closeout visits, and prepare corresponding monitoring reports.
- Verify the accuracy and quality of clinical trial data and ensure compliance with study protocols and ICHGCP requirements.
- Ensure proper management of investigator and pharmacy files, including filing and archiving activities within study documentation systems.
- Follow up on Serious Adverse Event (SAE) reporting and ensure site compliance with safety requirements.
- Communicate protocol-related information to investigational sites and support site teams throughout the study lifecycle.
- Act as a key liaison between study stakeholders, investigators, and clinical research teams while promoting Good Clinical Practices.
- Maintain study tracking tools and report site issues, risks, and improvement opportunities to the project team.
- Stay up to date with relevant medical, scientific, and pharmacological knowledge.
- Report regularly to the CRA Manager on study progress and site-related activities.
Le profil recherché
Why join us?
At Excelya, we combine a passion for science with the enthusiasm of teamwork to redefine excellence in healthcare.
Here's what makes us unique:
We are a young and ambitious healthcare company, bringing together 900 Excelyates, driven by the goal of becoming the leading mid-sized CRO in Europe, while offering the best employee experience.
Our "one-stop provider" service model-combining full-service, functional service provider, and consulting-allows you to grow through diverse and stimulating projects. By collaborating with leading experts, you will contribute to the development of scientific, operational, and human knowledge, all in service of improving the patient journey.
Excelling with kindness means evolving in an environment that values your natural talents, encourages boldness, pushes boundaries, and cultivates your potential, so that you can fully contribute to our shared mission.
- Strong experience in clinical trial monitoring.
- Significant experience in interventional clinical studies, preferably involving investigational medicinal products.
- Good understanding of the pharmaceutical industry environment and sponsor expectations.
- Experience in oncology and/or hematology is considered a strong asset.
- Experience working on complex clinical studies and/or high patient-enrollment studies is highly desirable.
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 22/10/2026 - Réf : e9102370-af61-4d88-8786-324cc19998ce
