Senior Clinical Research Associate

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

Résumé du poste

Une entreprise mondiale propose un poste de Clinical Research Associate (CRA) à Valence, France. Ce rôle exige une expérience de surveillance indépendante et offre un environnement de travail flexible. En tant que CRA, vous serez clé dans la gestion de plusieurs essais cliniques, en garantissant la conformité et la qualité des sites. Opportunités de croissance de carrière et avantages compétitifs attendent le candidat motivé.

Prestations

Environnement de travail flexible

Avantages de santé complets

Opportunités de développement de carrière

Exposition à des technologies innovantes

Qualifications

• Minimum 3 ans d'expérience en surveillance indépendante en tant que CRA.
• Fluent en français et anglais, écrit et parlé.
• Expérience en réalisant des visites de sites à travers plusieurs domaines thérapeutiques.

Responsabilités

• Effectuer des visites de qualification, d'initiation, de surveillance et de clôture des sites.
• Vérifier l'exactitude des données cliniques.
• Foster des relations professionnelles solides avec le personnel des sites.

Connaissances

Gestion des priorités

Connaissance des lignes directrices ICH-GCP

Formation

Diplôme de Bachelor en sciences de la santé ou de la vie

Description du poste

Senior Clinical Research Associate, valence

Client:

AL Solutions

Location:

valence, France

Job Category:

Other

-

EU work permit required:

Yes

Job Reference:

1637664170902028288327642

Job Views:

1

Posted:

02.06.2025

Expiry Date:

17.07.2025

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!

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