Clinical Research Associate
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Clinical Research Associate II – Paris (Home-Based)
Chloe O'Shea has partnered with a large global CRO renowned for delivering innovative, high-quality solutions in clinical development. We are seeking an experienced Clinical Research Associate II (CRA II) to join a dedicated single-sponsor team in Paris. This is an exciting opportunity to contribute to late-phase oncology studies within a leading sponsor environment, while enjoying the flexibility of a home-based position.
The Role
As a CRA II, you will be a key contributor to the successful delivery of clinical trials across Île-de-France. You will oversee site management activities, act as the primary liaison with investigative sites, and ensure strict compliance with study protocols, ICH-GCP, and local regulatory requirements. This role is well-suited to CRAs who are eager to deepen their expertise in oncology while working within a supportive, sponsor-dedicated team.
Key Responsibilities
- Independently manage qualification, initiation, monitoring, and close-out visits.
- Ensure compliance with ICH-GCP, local regulations, and sponsor SOPs.
- Perform source data verification, investigational product accountability, and maintain accurate site documentation.
- Build and maintain strong relationships with site staff, providing guidance and ongoing support.
- Proactively identify and resolve site-level challenges to keep studies on track.
- Maintain complete and accurate trial documentation in CTMS, eTMF, and EDC systems.
Requirements
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
- Minimum of 2 years of independent monitoring experience (CRO or pharmaceutical company).
- Experience in late-phase studies, ideally in oncology.
- Strong knowledge of ICH-GCP and French clinical trial regulations.
- Excellent communication, relationship-building, and organisational skills.
What’s in It for You?
This role offers a competitive salary and benefits package, flexible home-based working, and clear opportunities for career progression within one of the world’s largest CROs. You’ll gain valuable experience working on impactful late-phase oncology trials, while enjoying a collaborative culture that values professional development, work-life balance, and wellbeing.
If you are an experienced CRA looking to take the next step in your career, we’d love to hear from you. Apply today to join a global team dedicated to advancing clinical research and improving patients’ lives.
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