Senior Clinical Research Associate
On-siteRome, Lazio, Italy
Job Summary
Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conduct site visits to assess performance, resolve issues, and provide support for successful trial execution. Collaborate with cross-functional teams to guarantee timely data collection and reporting while offering training to site staff and other CRAs. Build effective relationships with site personnel and stakeholders to facilitate smooth operations. This role requires advanced life sciences or medical education, extensive CRA experience, and the ability to travel 60% of the time domestically and internationally. Based in Rome, Venice, or Florence, you will contribute to ICON's mission of accelerating new medicines to patients worldwide.
Required Qualifications
- Advanced degree in a relevant field such as life sciences, nursing, or medicine
- Extensive experience as a Clinical Research Associate
- Strong understanding of clinical trial processes and regulatory requirements
- Proven ability to manage multiple sites and projects simultaneously
- Strong organizational and problem-solving skills
- Expertise in monitoring practices
- Expertise in data integrity
- Expertise in site management
- Proficiency in relevant clinical trial software and tools
- Excellent communication skills
- Excellent interpersonal skills
- Stakeholder management skills
- Ability to influence and drive compliance within a complex environment
- Ability to travel at least 60% of the time (international and domestic - fly and drive)
- Valid driver's license
- Legal right to work in the country where the role is based
- Based in Rome, Venice or Florence
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