(Senior) Clinical Research Associate (CRA) - sponsor dedicated(m/w/x)

Beschreibung

In this role, you will drive clinical excellence by coordinating study activities and ensuring patient safety. You'll balance technical reporting with building vital relationships at research sites.

Anforderungen

• •University degree in medicine, science, or equivalent
• •Knowledge of ICH-GCP guidelines and medical data expertise
• •Excellent written and verbal English and German
• •Good social skills and timely query management
• •Ability to travel 60% and valid drivers license

Aufgaben

• •Coordinate all study setup and monitoring activities
• •Complete accurate study status reports
• •Maintain comprehensive study documentation
• •Resolve sponsor-generated queries efficiently
• •Manage and monitor study cost efficiency
• •Prepare and review study documentation
• •Conduct feasibility studies for new proposals
• •Build collaborative relationships with clinical investigators
• •Maintain strong connections with site staff
• •Ensure patient safety through protocol compliance
• •Adhere to regulatory requirements and procedures

Tools & Technologien

Benefits