Senior Clinical Research Associate (CRA) - Obesity study(m/w/x)

Beschreibung

You will drive the success of obesity clinical trials by overseeing site performance and data integrity. Your day-to-day involves balancing site visits with collaborative teamwork to ensure participant safety.

Anforderungen

• •Advanced degree in life sciences, nursing, or medicine
• •Extensive experience as Clinical Research Associate
• •Understanding of clinical trial processes and regulations
• •Ability to manage multiple sites and projects
• •Strong organizational and problem-solving skills
• •Expertise in monitoring practices and data integrity
• •Proficiency in clinical trial software and tools
• •Excellent communication and stakeholder management skills
• •Ability to influence and drive compliance
• •Willingness to travel at least 60%
• •Possession of a valid driver’s license
• •Fluency in German and English language

Aufgaben

• •Monitor clinical trial sites for protocol and GCP compliance
• •Conduct site visits to assess performance and resolve issues
• •Collaborate with cross-functional teams on data collection
• •Report trial data accurately and within established timelines
• •Train and guide site staff and fellow CRAs
• •Maintain high standards for clinical trial conduct
• •Build effective relationships with site personnel and stakeholders
• •Facilitate smooth trial operations through proactive communication

Tools & Technologien

Benefits