Clinical Research Associate

AL Solutions; Paris; Sur place; EUR 50 000 - 70 000; Plein temps

Avantages offerts par ce poste

Competitive salary

Flexible home-based working

Career progression opportunities

Résumé du poste

A global clinical research organization is seeking an experienced Clinical Research Associate II (CRA II) for a home-based role in Paris. You will manage clinical trials, ensuring adherence to protocols and building strong relationships with site staff. Ideal candidates have a Bachelor's degree in Life Sciences, at least 2 years of independent monitoring experience, and a solid understanding of ICH-GCP. This position offers a competitive salary, benefits, and opportunities for career progression, ensuring a balance between work-life and professional development.

Qualifications

• Minimum of 2 years of independent monitoring experience (CRO or pharmaceutical company).
• Experience in late-phase studies, ideally in oncology.

Responsabilités

• Independently manage qualification, initiation, monitoring, and close-out visits.
• Ensure compliance with ICH-GCP, local regulations, and sponsor SOPs.
• Perform source data verification and investigational product accountability.

Connaissances

Strong knowledge of ICH-GCP

Excellent communication skills

Relationship-building skills

Organisational skills

Formation

Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related field

Description du poste

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.