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
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