Freelance CRA Opportunity in Italy
Are you a Clinical Research Associate (CRA) looking for an exciting freelance opportunity? We are on the hunt for a dedicated and experienced professional to oversee clinical trial activities throughout Italy. This role is tailored for someone who has mastered site management, excels at ensuring protocol compliance, thrives when building relationships with key stakeholders in the pharmaceutical sector, and upholds ICH-GCP standards.
Key Responsibilities:
- Site Monitoring: Conduct regular visits to ensure all study protocols are met.
- Study Oversight: Manage studies from initiation through close-out while maintaining high-quality data collection.
- Regulatory Compliance: Guarantee adherence to both local and international regulatory mandates.
- Relationship Management: Cultivate strong connections with investigators and clinic staff members alike.
- Documentation & Reporting: Keep detailed records of visit reports, monitoring logs, etc., that reflect accuracy as well as timeliness.
Skills Required:
Clinical Trials Acumen: Deep understanding of managing multiple sites within clinical trials is essential
ICH-GCP Knowledge: Proficiency in Good Clinical Practice guidelines ensures quality control across all aspects of trial conduct
Risk Assessment Ability: Aptitude for identifying potential issues early on allows proactive handling before escalation becomes necessary
Stakeholder Engagement Skillset: Expertise in forging robust partnerships aids effective communication amongst various parties involved
