Senior Clinical Research Associate
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Overview
In this role you will lead clinical trial monitoring to ensure protocol adherence, regulatory compliance, and high-quality data. You will work with cross-functional teams to enable timely trial execution and provide training to site staff. You'll build strong relationships with site personnel to support smooth operations and continuous improvement. This position offers a global sponsor-dedicated environment with opportunities to influence trial outcomes and patient care.
Retribuzione / Benefits
- Competitive base salary
- Health and wellbeing programmes
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes
- Learning and development opportunities
Responsabilità
- Monitor clinical trial sites for protocol, GCP, and regulatory compliance
- Conduct site visits to assess performance and resolve issues
- Collaborate with cross-functional teams for timely data collection and reporting
- Provide training and guidance to site staff and fellow CRAs
- Build and maintain relationships with site personnel and stakeholders to enable smooth operations
Requisiti fondamentali
- Bachelor in a scientific or healthcare-related field
- Extensive experience as a Clinical Research Associate
- Proven ability to manage multiple sites and projects
- Expertise in monitoring, data integrity, and site management
- Proficiency in relevant clinical trial software and tools
- Excellent communication and stakeholder management
- Willingness to travel approximately 60%
- communication
- interpersonal skills
- problem-solving
- monitoring practices
- data integrity
- site management
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