Contract CRA: Site & Study Management Leader

Tigermed; Bordeaux; Sur place; EUR 35 000 - 50 000; Plein temps

Résumé du poste

A leading clinical research organization in Bordeaux is seeking a Clinical Research Associate to manage and oversee clinical studies from site selection to close-out. The ideal candidate will have a bachelor's degree in biomedical sciences and at least 2 years of experience in clinical research, particularly in medical device trials. Responsibilities include regulatory compliance, monitoring site performance, and ensuring high-quality data collection. This position requires good communication skills and proficiency in Microsoft Office.

Qualifications

• At least 2 years of CRA experience.
• Experience in at least 3 medical device clinical trials.
• Good written and oral English.

Responsabilités

• Assist IRB submissions and perform site selection.
• Conduct site initiation and ensure compliance with protocols.
• Track study recruitment and conduct monitoring visits.
• Ensure timely collection of essential documents and safety information.
• Finalize budgets and execute study payment schedules.

Connaissances

Good understanding of Good Clinical Practice

Proactive attitude

Teamwork ability

Formation

Bachelor's degree in biomedical / medical science

Outils

Microsoft Word

Microsoft Excel

PowerPoint

Outlook

Description du poste

A leading clinical research organization in Bordeaux is seeking a Clinical Research Associate to manage and oversee clinical studies from site selection to close-out. The ideal candidate will have a bachelor's degree in biomedical sciences and at least 2 years of experience in clinical research, particularly in medical device trials. Responsibilities include regulatory compliance, monitoring site performance, and ensuring high-quality data collection. This position requires good communication skills and proficiency in Microsoft Office.