A leading clinical research organization seeks a Clinical Research Associate to ensure seamless study execution and compliance. The ideal candidate has a science or healthcare background and at least 2 years of on-site monitoring experience, preferably in Haematology or Oncology.
Key Responsibilities:
• Monitor studies for adherence to regulatory requirements
• Collaborate with sponsors and trial sites to resolve issues
• Provide scientific expertise and guidance to trial sites
Requirements:
• Bachelor's degree in a relevant field (science or healthcare)
• At least 2 years of on-site monitoring experience
• Strong knowledge of clinical trials regulations and guidelines
Benefits:
• Opportunity to work in a dynamic environment with various teams
• Professional growth and development opportunities
What We Offer:
As a Clinical Research Associate, you will be part of a global team dedicated to delivering high-quality clinical trials. We offer a competitive salary, comprehensive benefits package, and opportunities for career advancement.
Apply now to join our team and contribute to the success of our clinical research organization!