Senior CRA
ICON
Senior Clinical Research Associate at ICON overseeing clinical trial monitoring in a sponsor-dedicated model. The role involves managing trial sites, ensuring protocol and regulatory compliance, and mentoring junior staff across multiple projects.
Responsibilities
- Monitor clinical trial sites for adherence to protocols, regulations, and GCP standards
- Conduct site visits to assess performance, resolve issues, and support trial execution
- Collaborate with cross-functional teams on accurate data collection and reporting
- Provide training and guidance to site staff and other CRAs on trial conduct standards
- Build and maintain relationships with site personnel and stakeholders for smooth operations
Requirements
- Bachelor's degree in scientific or healthcare-related discipline
- Extensive CRA experience with strong clinical trial process and regulatory knowledge
- Ability to manage multiple sites and projects with strong organizational skills
- Expertise in monitoring practices, data integrity, and clinical trial software
- Excellent communication and stakeholder management abilities
- Willingness to travel approximately 60% as required
Ledig stilling opslået Indrykket for 5 dage siden
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