Senior CRA (Sponsor dedicated)(m/w/x)

Beschreibung

You will drive clinical excellence by overseeing trial site compliance and data integrity. Your day-to-day involves visiting sites and mentoring staff to ensure every study meets the highest standards.

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
• •Ability to travel 60% of the time
• •Possession of a valid driver’s license

Aufgaben

• •Monitor clinical trial sites for protocol adherence
• •Ensure compliance with regulatory and GCP standards
• •Conduct site visits to assess performance
• •Resolve site issues to ensure trial execution
• •Collaborate with cross-functional teams for data reporting
• •Train and guide site staff and colleagues
• •Maintain high standards of clinical trial conduct
• •Build effective relationships with site personnel

Tools & Technologien

Benefits