Clinical Research Associate (CRA)

TN France; Boulogne-Billancourt; Hybride; EUR 35 000 - 55 000; Plein temps

Résumé du poste

An established industry player is seeking a dynamic Clinical Research Associate to join their team in Boulogne-Billancourt. This hybrid role combines the responsibilities of a Junior CRA and a Clinical Trial Site Coordinator, offering a unique opportunity to support clinical trials across multiple sites. The ideal candidate will ensure compliance with GCP standards while engaging with site staff and sponsors. If you are passionate about clinical research and eager to contribute to impactful studies, this position is perfect for you. Join a forward-thinking organization where your skills will make a real difference.

Qualifications

• 1+ year experience as CRA or relevant clinical research experience.
• Valid GCP/ISO14155 certification and knowledge of current regulations.

Responsabilités

• Conduct feasibility and site qualification visits.
• Act as the primary contact between Sponsor/CRO and the site.

Connaissances

Organizational Skills

Communication Skills

Data Entry Proficiency

Problem-Solving Skills

Formation

Bachelor’s degree in Life Sciences/Health/Pharmacy

Outils

eCRF Systems

Description du poste

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Clinical Research Associate (CRA), Boulogne-Billancourt

Client: VCLS

Location: Boulogne-Billancourt, France

Job Category: Other

EU work permit required: Yes

Job Reference: ceb48e51d921

Job Views: 3

Posted: 24.04.2025

Expiry Date: 08.06.2025

Job Description:

We are looking for a dynamic and motivated junior CRA/Clinical Study Coordinator to fill a hybrid position, combining responsibilities of a Junior Clinical Research Associate (CRA) (60%) and a Clinical Trial Site Coordinator (40%). The ideal candidate will support clinical trial activities across multiple sites, ensuring compliance with GCP and study protocols, while providing hands-on coordination and data entry support at the site level.

Junior CRA position :

• Conduct feasibility and site qualification visits
• Prepare and conduct site initiation visits, monitoring, and site closure in accordance with GCP and study procedures
• Write visit reports and contribute to study progress reports for the project team and sponsor
• Train the principal investigator and investigational team on the study protocol, documentation, and procedures
• Ensure investigator adherence to GCP standards
• Maintain proper filing and documentation in the Investigator Site File
• Retrieve essential documents for the Trial Master File
• Monitor patient enrollment and follow up on site performance
• Oversee materials and products at sites, including returns
• Perform source data verification and ensure data quality
• Support regulatory document reviews as part of EU legal activities

Clinical trial site coordinator position:

• Act as the primary contact between Sponsor/CRO and the site
• Track patient enrollment and support site in achieving goals
• Perform data entry into eCRF and address queries
• Maintain site documentation and regulatory compliance
• Assist in scheduling and preparing for monitoring visits, audits, and inspections

Requirements:

• Bachelor’s degree in Life Sciences/Health/Pharmacy
• Valid GCP/ISO14155 certification and knowledge of current regulations
• At least 1-year experience as CRA or relevant clinical research experience
• Excellent organizational and multitasking skills
• Strong communication skills for engaging with site staff and sponsors
• Proficiency in data entry and eCRF systems
• Problem-solving skills and attention to detail