Senior Clinical Research Associate (Oncology Experience Preferred) - Remote

Overview

The Senior Clinical Research Associate at Parexel is responsible for ensuring data integrity and compliance with regulatory standards while conducting clinical trials, primarily through remote monitoring.

In Short

• Responsible for data integrity and quality in clinical trials.
• Ensure compliance with ICH GCP and local regulations.
• Conduct monitoring activities both remotely and on-site.
• Collaborate with site managers and investigators.
• Manage protocol deviations and follow-up reporting.
• Verify informed consent processes and subject safety.
• Document monitoring activities and ensure project timelines are met.
• Participate in global clinical monitoring and project meetings.
• Build effective relationships with stakeholders.
• Adapt to changing technologies and processes.

Requirements

• Bachelor’s degree or Registered Nurse (RN) in a related field.
• Excellent communication skills, both verbal and written.
• Proficiency in local language and fluency in English.
• Experience in clinical research and monitoring.
• Ability to adapt to changing environments.
• Strong networking and relationship-building skills.
• Knowledge of clinical trial protocols and compliance standards.
• Ability to manage multiple tasks and priorities.
• Experience with data management and reporting.
• Understanding of patient welfare and ethical considerations in research.

Benefits

• Opportunity to contribute to improving global health.
• Flexible working arrangements including remote work.
• Supportive team environment.
• Access to professional development and training.
• Participation in significant clinical trials.
• Networking opportunities within the healthcare industry.
• Competitive compensation package.
• Work with a diverse and global team.
• Access to company resources and tools for success.
• Engagement in meaningful work that impacts patient lives.