Senior CRA

Responsibilities

• Monitor clinical trial sites for adherence to protocols and standards
• Conduct site visits to assess performance and resolve issues
• Collaborate with cross-functional teams for data collection and reporting
• Provide training and guidance to site staff and CRAs
• Build and maintain relationships with site personnel and stakeholders

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Extensive experience as a Clinical Research Associate
• Strong understanding of clinical trial processes and regulatory requirements
• Prioritization of managing multiple sites and projects simultaneously
• Expertise in monitoring practices and data integrity
• Excellent communication and stakeholder management skills
• Willingness to travel approximately 60%

Benefits

• Comprehensive total rewards package
• Health and wellbeing programmes including medical, dental, and vision coverage
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes
• Learning and development opportunities through structured training

Our client is an equal opportunity employer.