Senior Clinical Research Associate
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
* 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