Senior Clinical Research Associate

JR France; Dijon; Sur place; EUR 40 000 - 55 000; Plein temps

Résumé du poste

Une entreprise mondiale de recherche clinique recrute un Clinical Research Associate (CRA) pour rejoindre son équipe en France. Ce rôle permet des visites de sites gérables, avec une forte relation avec les sites et le sponsor, pour assurer la conformité et la qualité des essais. Avec une expérience requise de 3 ans, notamment en ICH-GCP, ce poste offre des opportunités de carrière et une rémunération compétitive.

Prestations

Salaire compétitif avec avantages supplémentaires

Opportunités de croissance de carrière

Environnement de travail flexible

Programmes de santé et de bien-être

Qualifications

• Au moins 3 ans d'expérience indépendante en suivi comme CRA.
• Expérience dans la conduite de visites de site dans plusieurs domaines thérapeutiques.

Responsabilités

• Effectuer des visites de qualification, d'initiation et de suivi.
• Assurer la conformité des sites cliniques aux directives ICH-GCP et réglementaires.
• Vérifier l'exactitude des données cliniques et gérer les produits d'investigation.

Connaissances

Organisation

Gestion des priorités

Connaissance des directives ICH-GCP

Bilingue en français et anglais

Formation

Diplôme en sciences de la santé ou de la vie

Description du poste

Client:

AL Solutions

Location:

Job Category:

Other

-

EU work permit required:

Yes

Job Reference:

1637664170902028288327614

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!