Clinical Research Associate

3 settimane fa


Milano, Lombardia, Italia Thermo Fisher Scientific A tempo pieno

Clinical Trial Coordinator Role

At Thermo Fisher Scientific, we're committed to enabling our customers to make the world healthier, cleaner and safer. As a Clinical Trial Coordinator, you'll play a crucial role in supporting our project teams, coordinating non-clinical responsibilities, and ensuring the smooth execution of clinical trials.

Key Responsibilities:

  • Perform PPD investigator file reviews and logging of outstanding issues in project-related tracking tools
  • Review regulatory documents for proper content
  • Liaise with monitor and investigative sites to resolve outstanding regulatory issues
  • Disseminate study-related information to clients, clinical study teams, and other PPD departments
  • Ensure adherence to Good Clinical Practices, country-specific regulations, and PPD/Client Standard Operating Procedures

Requirements:

  • Master's degree in a clinical specialism or equivalent education, training, and experience
  • Experience with submissions to Ethics Committees and Regulatory bodies (desired)
  • Ability to analyze project-specific data/systems to ensure accuracy and efficiency
  • Experience managing multiple projects with differing priorities
  • Exceptional communication, collaboration, organizational, and time management skills

What We Offer:

At Thermo Fisher Scientific, we value our employees' growth and development. We offer an award-winning learning and development program, ensuring you reach your potential. Our benefits package is designed to support your health and well-being, and we prioritize a work-life balance. Join our team and discover a collaborative environment where you can share expertise and have fun together.



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