Senior Clinical Research Associate - Oncology - Remote

Overview

The Senior Clinical Research Associate (CRA) is responsible for managing clinical studies at allocated sites, ensuring compliance with international guidelines and local regulations, and collaborating with study teams to achieve study commitments.

In Short

• Manage site selection and start-up processes.
• Conduct monitoring visits both remotely and onsite.
• Ensure sites are compliant with ICH-GCP and local regulations.
• Support investigators and site staff in study-related matters.
• Prepare and finalize monitoring visit reports.
• Conduct risk assessments and adapt monitoring intensity.
• Maintain accurate study documentation and data integrity.
• Collaborate with local Medical Science Liaisons as needed.
• Participate in quality checks and audits.
• Provide feedback on research-related information.

Requirements

• Bachelor’s degree in life sciences or related field.
• Excellent attention to detail and communication skills.
• Knowledge of ICH-GCP and local regulations.
• Ability to manage multiple tasks with conflicting deadlines.
• Proficient in written and spoken English.
• Experience in clinical trial monitoring.
• Ability to work in a remote environment.
• Good analytical and problem-solving skills.
• Flexibility to adapt to changing demands.
• Ability to travel nationally/internationally as required.

Benefits

• Opportunity to contribute to improving global health.
• Work with a diverse and dedicated team.
• Access to professional development resources.
• Flexible working environment.
• Competitive compensation package.