Senior Clinical Research Associate (Oncology Experience Preferred) - Remote

Overview

The Senior Clinical Research Associate (CRA) at Parexel will ensure data integrity and compliance with regulatory standards while conducting monitoring activities primarily remotely.

In Short

• Responsible for data integrity and quality at clinical sites.
• Conduct monitoring in line with Study Monitoring Plan.
• Collaborate with Site Manager for compliance assurance.
• Ensure adherence to ICH GCP and local regulations.
• Perform source document review and verification.
• Manage reporting of protocol deviations.
• Document activities per SOPs and project requirements.
• Participate in global monitoring and project meetings.
• Build relationships with site staff and stakeholders.
• Adapt to changing technologies and processes.

Requirements

• Bachelor’s degree or RN in a related field.
• Experience in clinical research and monitoring.
• Excellent verbal and written communication skills.
• Fluency in English and proficiency in local language.
• Strong networking and relationship-building abilities.
• Able to adapt to changing technologies.
• Effective problem-solving skills.
• Understanding of regulatory compliance and GCP guidelines.
• Ability to work independently and manage multiple tasks.
• Experience in oncology preferred.

Benefits

• Opportunity to contribute to improving global health.
• Work with a dedicated and empathetic team.
• Engagement in innovative clinical studies.
• Access to extensive training and development.
• Flexible work environment with remote options.
• Competitive compensation package.
• Collaborative and supportive workplace culture.
• Global exposure to clinical research practices.
• Participation in impactful projects.
• Career advancement opportunities.