Senior Clinical Research Associate

As a Senior Clinical Research Associate, you will oversee and manage clinical trial activities focused in Oncology to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.

Requirements

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Minimum 5 years of experience as CRA with a strong understanding of clinical trial processes and regulatory requirements in the Oncology field
• Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
• Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
• Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment

Benefits

• 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