Senior Clinical Research Associate

JR France; Chambéry; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading global CRO is looking for an experienced Clinical Research Associate (CRA) to conduct site visits and ensure compliance with clinical trial protocols across France. This role allows for flexible working conditions while offering opportunities for career growth and exposure to innovative methodologies in the clinical research field.

Prestations

Competitive salary with additional benefits

Opportunities for career growth

Flexible working environment

Comprehensive health benefits

Qualifications

• At least 3 years of independent monitoring experience as a CRA.
• Strong knowledge of ICH-GCP guidelines and French regulatory requirements.
• Experience in conducting site visits across multiple therapeutic areas.

Responsabilités

• Perform site qualification, initiation, monitoring, and close-out visits.
• Ensure compliance with ICH-GCP guidelines and protocol-specific requirements.
• Maintain essential trial documentation and update systems like CTMS and EDC.

Connaissances

Organizational Skills

Monitoring Experience

Knowledge of ICH-GCP

Fluency in French and English

Formation

Bachelor’s degree in health or life sciences

Description du poste

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Client:

AL Solutions

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

1637664170902028288327641

Job Views:

1

Posted:

02.06.2025

Expiry Date:

17.07.2025

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Job Description:

Chloe O'Shea is proud to partner with a leading global CRO providing innovative clinical trial solutions. We are seeking an experienced Clinical Research Associate (CRA) to join a dedicated team based in France for a single-sponsor opportunity in CNS. This role offers a manageable workload of 5-8 site visits per month , allowing you to focus on high-quality monitoring and site management.

The Role

As a Clinical Research Associate (CRA) , you will play a key role in driving the success of clinical trials across France. Collaborating with the sponsor and investigative sites, you will ensure compliance with protocols, GCP guidelines, and regulatory requirements. With a focus on building strong site relationships, this position is ideal for professionals passionate about advancing clinical research in a supportive and innovative environment.

Key Responsibilities

• Perform site qualification, initiation, routine monitoring, and close-out visits across France.
• Ensure clinical sites adhere to ICH-GCP guidelines, applicable regulations, and protocol-specific requirements.
• Verify the accuracy and integrity of clinical data and oversee the management of investigational products (IP).
• Identify, resolve, and escalate site-related issues to ensure timely and efficient trial progress.
• Foster and maintain strong professional relationships with site staff and sponsor representatives.
• Provide training and guidance to site staff to ensure protocol compliance and study quality.
• Maintain essential trial documentation and update systems such as CTMS, eTMF, and EDC.

Requirements

• A Bachelor’s degree in a health or life sciences discipline.
• At least 3 years of independent monitoring experience as a CRA
• Strong knowledge of ICH-GCP guidelines and French regulatory requirements.
• Experience in conducting site visits and monitoring activities across multiple therapeutic areas.
• Fluent in French and English , both written and spoken.
• Strong organizational skills and ability to manage priorities effectively.

What’s in It for You?

• Competitive salary with additional benefits.
• Opportunities for career growth within a global organization.
• Flexible working environment with manageable travel requirements.
• Exposure to innovative technologies and methodologies in clinical research.
• Comprehensive health benefits and wellness programs.

If you are a motivated professional looking to advance your career as a Clinical Research Associate, we would love to hear from you. Apply now and join a team dedicated to driving innovation in clinical trials!