Senior CRA

• Monitor clinical trial sites for adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
• Conduct site visits to assess site performance, resolve issues, and support successful trial execution
• Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting
• Provide training and guidance to site staff and other CRAs
• Build and maintain effective relationships with site personnel and stakeholders
• Oversee and manage clinical trial activities throughout the study lifecycle
• Ensure data integrity, participant safety, and compliance

• Advanced degree in a relevant field such as life sciences, nursing, or medicine
• Extensive experience as a Clinical Research Associate, with a 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, data integrity, and site management
• Proficiency in relevant clinical trial software and tools
• Excellent communication, interpersonal, and stakeholder management skills
• Ability to influence and drive compliance within a complex environment
• Ability to travel at least 60% of the time, internationally and domestically, by air and car
• Valid driver’s license
• Legal right to work in the country where the role is based

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways